Skip to main content
main-content
Top

Tip

Swipe om te navigeren naar een ander hoofdstuk

2014 | OriginalPaper | Hoofdstuk

Aangeboren afwijkingen van het spraakorgaan

maart 2002

Auteurs: H.F.M. Peters, R. Bastiaanse, J. Van Borsel, K. Jansonius-Schultheiss, Sj. Van der Meulen, B.J.E. Mondelaers

Gepubliceerd in: Perifere articulatiestoornissen

Uitgeverij: Bohn Stafleu van Loghum

share
DELEN

Deel dit onderdeel of sectie (kopieer de link)

  • Optie A:
    Klik op de rechtermuisknop op de link en selecteer de optie “linkadres kopiëren”
  • Optie B:
    Deel de link per e-mail

Samenvatting

Het spraakorgaan wordt onderverdeeld in drie verschillende systemen: a het articulatorisch systeem, b het fonatiesysteem en c het respiratoir systeem. Het articulatorische systeem omvat de mond- en keelholte; met het fonatiesysteem worden hoofdzakelijk de stembanden en larynx bedoeld; het respiratoir systeem verwijst naar de respiratoire tractus distaal van de larynx.
Literatuur
go back to reference Agosti, E., Filippi, G., & Chiussi, F. (1974). Generalized familial bronchomalacia. Acta Paediatrica Scandinavica, 63, 616-618. Agosti, E., Filippi, G., & Chiussi, F. (1974). Generalized familial bronchomalacia. Acta Paediatrica Scandinavica, 63, 616-618.
go back to reference Auchterlonie, I.A., & White, M.P. (1982). Recurrence of the vater association within a sibship. Clinical Genetics, 21, 122-124. Auchterlonie, I.A., & White, M.P. (1982). Recurrence of the vater association within a sibship. Clinical Genetics, 21, 122-124.
go back to reference Bamshad, M., Lin, R.C., Law, D.J., e.a. (1997). Mutations in human tbx3 alter limb, apocrine and genital development in ulnar-mammary syndrome. Nature Genetics, 16, 311-315. Bamshad, M., Lin, R.C., Law, D.J., e.a. (1997). Mutations in human tbx3 alter limb, apocrine and genital development in ulnar-mammary syndrome. Nature Genetics, 16, 311-315.
go back to reference Belmont, J.R., & Grundfast, K. (1984). Congenital laryngeal stridor (laryngomalacia): etiologic factors and associated disorders. Annals of Otology Rhinology and Laryngology, 93, 430-437. Belmont, J.R., & Grundfast, K. (1984). Congenital laryngeal stridor (laryngomalacia): etiologic factors and associated disorders. Annals of Otology Rhinology and Laryngology, 93, 430-437.
go back to reference Benjamin, B., Pitkin, J., & Cohen, D. (1981). Congenital tracheal stenosis. Annals of Otology Rhinology and Laryngology, 90, 364-371. Benjamin, B., Pitkin, J., & Cohen, D. (1981). Congenital tracheal stenosis. Annals of Otology Rhinology and Laryngology, 90, 364-371.
go back to reference Biesecker, L.G., Abbott, M., Allen, J., e.a. (1996). Report from the workshop on Pallister- Hall syndrome and related phenotypes. American Journal of Medical Genetics, 65, 76-81. Biesecker, L.G., Abbott, M., Allen, J., e.a. (1996). Report from the workshop on Pallister- Hall syndrome and related phenotypes. American Journal of Medical Genetics, 65, 76-81.
go back to reference Bray, R.J., & Lamb, W.H. (1988). Tracheal stenosis or agenesis in association with tracheooesophageal fistula and oesophageal atresia. Anaesthesia, 43, 654-658. Bray, R.J., & Lamb, W.H. (1988). Tracheal stenosis or agenesis in association with tracheooesophageal fistula and oesophageal atresia. Anaesthesia, 43, 654-658.
go back to reference Brenner, K.E., Oca, M.J., & Donn, S.M. (2000). Congenital choanal atresia in siblings. Journal of Perinatology 2000, 20, 443-444. Brenner, K.E., Oca, M.J., & Donn, S.M. (2000). Congenital choanal atresia in siblings. Journal of Perinatology 2000, 20, 443-444.
go back to reference Buzenet, C., Hamel-Teillac, D., Acar, P., e.a. (2000). Facial hemangioma associated with arterial and eye abnormalities and coarctatio aorta: phaces syndrome. Annales de Dermatologie et de Venereologie, 127, 292-295. Buzenet, C., Hamel-Teillac, D., Acar, P., e.a. (2000). Facial hemangioma associated with arterial and eye abnormalities and coarctatio aorta: phaces syndrome. Annales de Dermatologie et de Venereologie, 127, 292-295.
go back to reference Chen, H., Chang, C.H., Perrin, E., & Perrin, J. (1982). A lethal, Larsen-like multiple joint dislocation syndrome. American Journal of Medical Genetics, 13, 149-161. Chen, H., Chang, C.H., Perrin, E., & Perrin, J. (1982). A lethal, Larsen-like multiple joint dislocation syndrome. American Journal of Medical Genetics, 13, 149-161.
go back to reference Cohen, M.M. (1991). Hallermann-Streiff syndrome: a review. American Journal of Medical Genetics, 41, 488-499. Cohen, M.M. (1991). Hallermann-Streiff syndrome: a review. American Journal of Medical Genetics, 41, 488-499.
go back to reference Cohen, M.M. (1997). The child with multiple birth defects. New York: Oxford University Press. Cohen, M.M. (1997). The child with multiple birth defects. New York: Oxford University Press.
go back to reference Cooley, W.C., & Graham, J.M. (1991). Down syndrome: an update and review for the primary pediatrician. Clinical Pediatrics, 30, 233-253 Cooley, W.C., & Graham, J.M. (1991). Down syndrome: an update and review for the primary pediatrician. Clinical Pediatrics, 30, 233-253
go back to reference Cunningham, M.J., Eavey, R.D., & Shannon, D.C. (1985). Familial vocal cord dysfunction. Pediatrics, 76, 750-753. Cunningham, M.J., Eavey, R.D., & Shannon, D.C. (1985). Familial vocal cord dysfunction. Pediatrics, 76, 750-753.
go back to reference Davenport, S.L.H., Hefner, M.A., & Mitchell, J.A. (1986). The spectrum of clinical features in charge syndrome. Clinical Genetics, 29, 298-310. Davenport, S.L.H., Hefner, M.A., & Mitchell, J.A. (1986). The spectrum of clinical features in charge syndrome. Clinical Genetics, 29, 298-310.
go back to reference De Lorimer, A.A., & Harrison, M.R. (1985). Oesophageal atresia: embryogenesis and managment. World Journal of Surgery, 9, 250. De Lorimer, A.A., & Harrison, M.R. (1985). Oesophageal atresia: embryogenesis and managment. World Journal of Surgery, 9, 250.
go back to reference Devriendt, K., Swillen, A., & Fryns, J.P. (1996). Het velocardiofaciaal syndroom: een frequente genetische aandoening veroorzaakt door microdeleties in chromosoom 22q11. Tijdschrift voor Geneeskunde, 52, 511-521. Devriendt, K., Swillen, A., & Fryns, J.P. (1996). Het velocardiofaciaal syndroom: een frequente genetische aandoening veroorzaakt door microdeleties in chromosoom 22q11. Tijdschrift voor Geneeskunde, 52, 511-521.
go back to reference D’Hooghe, I., Lemmerling, M., Lagache, M., e.a. (1998). Otological manifestations of Charge syndrome. Annals of Otology Rhinology and Laryngology, 107, 935-941. D’Hooghe, I., Lemmerling, M., Lagache, M., e.a. (1998). Otological manifestations of Charge syndrome. Annals of Otology Rhinology and Laryngology, 107, 935-941.
go back to reference Evans, J.N. (1985). Management of the cleft larynx and tracheoesophageal clefts. Annals of Otology Rhinology and Laryngology, 94, 627-30. Evans, J.N. (1985). Management of the cleft larynx and tracheoesophageal clefts. Annals of Otology Rhinology and Laryngology, 94, 627-30.
go back to reference Finlay, H.V. (1955). Familial congenital stridor. Archives of Disease in Childhood, 24, 219-223. Finlay, H.V. (1955). Familial congenital stridor. Archives of Disease in Childhood, 24, 219-223.
go back to reference Fitzsimmons, J.S., Fitzsimmons, E.M., Barrow, M., & Gilbert, G.B. (1982). Fronto-metaphyseal dysplasia: further delineation of the clinical syndrome. Clinical Genetics, 22, 195-205. Fitzsimmons, J.S., Fitzsimmons, E.M., Barrow, M., & Gilbert, G.B. (1982). Fronto-metaphyseal dysplasia: further delineation of the clinical syndrome. Clinical Genetics, 22, 195-205.
go back to reference Fraser, F.C. (1970). The genetics of cleft lip and cleft palate. American Journal of Human Genetics, 22, 336-352. Fraser, F.C. (1970). The genetics of cleft lip and cleft palate. American Journal of Human Genetics, 22, 336-352.
go back to reference Fraser, C., Baird, P.A., & Sadovnick, A.D. (1987). A comparison of incidence trends for esophageal atresia and tracheoesophagal fistula, and infectious disease. Teratology, 36, 363-369. Fraser, C., Baird, P.A., & Sadovnick, A.D. (1987). A comparison of incidence trends for esophageal atresia and tracheoesophagal fistula, and infectious disease. Teratology, 36, 363-369.
go back to reference Gorlin, R.J., Cohen, M.M., & Levin, L.S. (1990). Syndromes of the head and neck. Oxford: Oxford University Press. Gorlin, R.J., Cohen, M.M., & Levin, L.S. (1990). Syndromes of the head and neck. Oxford: Oxford University Press.
go back to reference Gripp, K.W., Wotton, D., Edwards, M.C., e.a. (2000). Mutations in tgif cause holoprosencephaly and link nodal signalling to human neural axis development. Nature Genetics, 25, 205-208. Gripp, K.W., Wotton, D., Edwards, M.C., e.a. (2000). Mutations in tgif cause holoprosencephaly and link nodal signalling to human neural axis development. Nature Genetics, 25, 205-208.
go back to reference Harris, J., Robert, E., & Kallen, B. (1997). Epidemiology of choanal atresia with special reference to the charge association. Pediatrics, 99, 363-7. Harris, J., Robert, E., & Kallen, B. (1997). Epidemiology of choanal atresia with special reference to the charge association. Pediatrics, 99, 363-7.
go back to reference Hawkins, D.B., Liu-Shindo, M., Kahlstrom, E.J., & MacLaughlin, E.F. (1990). Familial vocal cord dysfunction associated with digital anomalies. Laryngoscope, 100, 1001-1004. Hawkins, D.B., Liu-Shindo, M., Kahlstrom, E.J., & MacLaughlin, E.F. (1990). Familial vocal cord dysfunction associated with digital anomalies. Laryngoscope, 100, 1001-1004.
go back to reference Kang, S., Graham, J.M., Olney, A.H., & Biesecker, L.G. (1997). gli3 frameshift mutations cause autosomal dominant Pallister-Hall syndrome. Nature Genetics, 15, 266-268. Kang, S., Graham, J.M., Olney, A.H., & Biesecker, L.G. (1997). gli3 frameshift mutations cause autosomal dominant Pallister-Hall syndrome. Nature Genetics, 15, 266-268.
go back to reference Keeling, J.W. (1993). Fetal and neonatal pathology. London: Springer-Verlag. Koppel, R., Friedman, S., & Fallet, S. (1996). Congenital vocal cord paralysis with possible autosomal dominant recessive inheritance: case report and review of the literature. American Journal of Medical Genetics, 64, 485-487. Keeling, J.W. (1993). Fetal and neonatal pathology. London: Springer-Verlag. Koppel, R., Friedman, S., & Fallet, S. (1996). Congenital vocal cord paralysis with possible autosomal dominant recessive inheritance: case report and review of the literature. American Journal of Medical Genetics, 64, 485-487.
go back to reference Lacassie, Y., & Arriaza, M.I. (1996). Opitz gbbb syndrome and the 22q11.2 deletion. American Journal of Medical Genetics, 62, 318. Lacassie, Y., & Arriaza, M.I. (1996). Opitz gbbb syndrome and the 22q11.2 deletion. American Journal of Medical Genetics, 62, 318.
go back to reference Larrandaburu, M., Schuler, L., Ehlers, J.A., Reis, A.M., & Silveira, E.L. (1999). The occurence of Poland and Poland-Moebius syndromes in the same family: further evidence of their genetic component. Clinical Dysmorphology, 8, 93-99. Larrandaburu, M., Schuler, L., Ehlers, J.A., Reis, A.M., & Silveira, E.L. (1999). The occurence of Poland and Poland-Moebius syndromes in the same family: further evidence of their genetic component. Clinical Dysmorphology, 8, 93-99.
go back to reference Larsen, W.J. (1993). Human embryology. New York: Churchill Livingstone. Maslova, I.V., Solonichenko, V.G., Sodatskii, I.U.L., & Onufrieva, E.K. (1999). Genetic aspects of congenital pathology of the larynx and trachea. Vestn Otorinolaryngol, 2, 30-33. Larsen, W.J. (1993). Human embryology. New York: Churchill Livingstone. Maslova, I.V., Solonichenko, V.G., Sodatskii, I.U.L., & Onufrieva, E.K. (1999). Genetic aspects of congenital pathology of the larynx and trachea. Vestn Otorinolaryngol, 2, 30-33.
go back to reference McDonld-McGinn, D.M., La Rossa, D., e.a. (1997). The 22q11.2 deletetion : screening, diagnostic workup, and outcome of results: reports on 181 patients. Genetic Testing, 1, 99-108. McDonld-McGinn, D.M., La Rossa, D., e.a. (1997). The 22q11.2 deletetion : screening, diagnostic workup, and outcome of results: reports on 181 patients. Genetic Testing, 1, 99-108.
go back to reference Miettinen, P.J., Chin, J.R., Shum, L., e.a. (1999). Epidermal growth factor receptor function is necessary for normal craniofacial development and palate closure. Nature Genetics, 22, 69-73. Miettinen, P.J., Chin, J.R., Shum, L., e.a. (1999). Epidermal growth factor receptor function is necessary for normal craniofacial development and palate closure. Nature Genetics, 22, 69-73.
go back to reference Melnick, M., Bixler, D., Fogh-Andersen, P., e.a. (1980). Cleft lip (cleft palate: An overview of the literature and an analysis of Danish cases born between 1941 and 1968). American Journal of Medical Genetics, 6, 83-97. Melnick, M., Bixler, D., Fogh-Andersen, P., e.a. (1980). Cleft lip (cleft palate: An overview of the literature and an analysis of Danish cases born between 1941 and 1968). American Journal of Medical Genetics, 6, 83-97.
go back to reference mim. Mendelian Inheritance in Man; web-URL: http://​www.​ncbi.​nlm.​nih.​gov/​O mim mim. Mendelian Inheritance in Man; web-URL: http://​www.​ncbi.​nlm.​nih.​gov/​O mim
go back to reference Mitchell, D.B., Irwin, C., Bailey, C.M., & Evans, N.G. (1987). Cysts of the infants larynx. Journal of Laryngology and Otology, 101, 833-837. Mitchell, D.B., Irwin, C., Bailey, C.M., & Evans, N.G. (1987). Cysts of the infants larynx. Journal of Laryngology and Otology, 101, 833-837.
go back to reference Mostafa, S.M. (1976). Variation in subglottic size in children. Proceedings of the Royal Society of Medicine, 69, 793. Mostafa, S.M. (1976). Variation in subglottic size in children. Proceedings of the Royal Society of Medicine, 69, 793.
go back to reference Oley, C.A., Baraitser, M., & Grant, D.B. (1988). A reappraisal of the charge association. Journal of Medical Genetics, 25, 147-157. Oley, C.A., Baraitser, M., & Grant, D.B. (1988). A reappraisal of the charge association. Journal of Medical Genetics, 25, 147-157.
go back to reference Ondrey, F., Griffith, A., Van Waes, C., e.a. (2000). Asymptomatic laryngeal malformations are common in patients with Pallister-Hall syndrome. American Journal of Medical Genetics, 91, 64-67. Ondrey, F., Griffith, A., Van Waes, C., e.a. (2000). Asymptomatic laryngeal malformations are common in patients with Pallister-Hall syndrome. American Journal of Medical Genetics, 91, 64-67.
go back to reference Parnell, F.W., & Brandenberg, J.H. (1970). Vocal Cord paralysis: a review of 100 cases. Laryngoscope, 80, 1036-1045. Parnell, F.W., & Brandenberg, J.H. (1970). Vocal Cord paralysis: a review of 100 cases. Laryngoscope, 80, 1036-1045.
go back to reference Phelan, P.D., Stocks, J.G., Williams, H.E., & Danks, D.M. (1973). Familial occurrence of congenital laryngeal clefts. Archives of Disease in Childhood, 48, 275-278. Quaderi, N.A., Schweiger, S., Gaudenz, K., e.a. (1997). Opitz g/bbb syndrome, a defect of midline development, is due to mutations in a new ring finger gene on Xp22. Nature Genetics, 17, 285-291. Phelan, P.D., Stocks, J.G., Williams, H.E., & Danks, D.M. (1973). Familial occurrence of congenital laryngeal clefts. Archives of Disease in Childhood, 48, 275-278. Quaderi, N.A., Schweiger, S., Gaudenz, K., e.a. (1997). Opitz g/bbb syndrome, a defect of midline development, is due to mutations in a new ring finger gene on Xp22. Nature Genetics, 17, 285-291.
go back to reference Ramos-Arroyo, M.A., Valiente, A., Rodriguez-Toral, E., e.a. (2000). Familial choanal atresia with maxillary hypoplasia, prognathism, and hypodontia. American Journal of Medical Genetics, 95, 237-240. Ramos-Arroyo, M.A., Valiente, A., Rodriguez-Toral, E., e.a. (2000). Familial choanal atresia with maxillary hypoplasia, prognathism, and hypodontia. American Journal of Medical Genetics, 95, 237-240.
go back to reference Richardson, M.A., & Cotton, R.T. (1984). Anatomic abnormalities of the pediatric airway. Pediatric Clinics of North America, 31, 821-834. Richardson, M.A., & Cotton, R.T. (1984). Anatomic abnormalities of the pediatric airway. Pediatric Clinics of North America, 31, 821-834.
go back to reference Salbert, B.A., Stevens, C.A., & Spence, J.E. (1991). Tracheomalacia in Hallermann-Streiff syndrome. American Journal of Medical Genetics, 41, 521-523. Salbert, B.A., Stevens, C.A., & Spence, J.E. (1991). Tracheomalacia in Hallermann-Streiff syndrome. American Journal of Medical Genetics, 41, 521-523.
go back to reference Scherer, N.J., D’Antonio, L.L., & Kalbfleissch, J.H. (1999). Early Speech and Language Development in Children with Velocardiofacial Syndrome. American Journal of Medical Genetics (Neuropsychiatric Genetics), 88, 714-723. Scherer, N.J., D’Antonio, L.L., & Kalbfleissch, J.H. (1999). Early Speech and Language Development in Children with Velocardiofacial Syndrome. American Journal of Medical Genetics (Neuropsychiatric Genetics), 88, 714-723.
go back to reference Schinzel, A. (1987). Ulnar-mammary syndrome. Journal of Medical Genetics, 24, 778-781. Schinzel, A. (1987). Ulnar-mammary syndrome. Journal of Medical Genetics, 24, 778-781.
go back to reference Sedano, H.O., & Gorlin, R.J. (1988). Opitz oculo-genital-laryngeal syndrome (Opitz bbb/gcompound syndrome). (Letter) American Journal of Medical Genetics, 30, 847-849. Sedano, H.O., & Gorlin, R.J. (1988). Opitz oculo-genital-laryngeal syndrome (Opitz bbb/gcompound syndrome). (Letter) American Journal of Medical Genetics, 30, 847-849.
go back to reference Shprintzen, R.J., Goldberg, R.B., Lewin, M.L., e.a. (1978). A new syndrome involving cleft palate, cardiac anomalies, typical facies, and learning disabilities: velo-cardio-facial syndrome. Cleft Palate Journal, 15, 56-62. Shprintzen, R.J., Goldberg, R.B., Lewin, M.L., e.a. (1978). A new syndrome involving cleft palate, cardiac anomalies, typical facies, and learning disabilities: velo-cardio-facial syndrome. Cleft Palate Journal, 15, 56-62.
go back to reference Shprintzen, R.J., Siegel-Sadewitz, V.L., Amato, J., & Goldberg, R.B. (1985). Anomalies associated with cleft lip, cleft palate, or both. American Journal of Medical Genetics, 20, 585-595. Shprintzen, R.J., Siegel-Sadewitz, V.L., Amato, J., & Goldberg, R.B. (1985). Anomalies associated with cleft lip, cleft palate, or both. American Journal of Medical Genetics, 20, 585-595.
go back to reference Shohat, M., Sivan, Y., Taub, E., & Davidson, S. (1992). Autosomal dominant congenital laryngomalacia. American Journal of Medical Genetics, 42, 813-814. Shohat, M., Sivan, Y., Taub, E., & Davidson, S. (1992). Autosomal dominant congenital laryngomalacia. American Journal of Medical Genetics, 42, 813-814.
go back to reference Shulman, J.B., Hollister, D.W., Thibeault, D.W., e.a. (1976). Familial laryngomalacia: a case report. Laryngoscope, 86, 84-91. Shulman, J.B., Hollister, D.W., Thibeault, D.W., e.a. (1976). Familial laryngomalacia: a case report. Laryngoscope, 86, 84-91.
go back to reference Stevenson, R.E., Hall, J.G., & Goodman, R.M. (1993). Human malformations and related anomalies. Oxford: Oxford University Press. Stevenson, R.E., Hall, J.G., & Goodman, R.M. (1993). Human malformations and related anomalies. Oxford: Oxford University Press.
go back to reference Stoler, J.M., Ladoulis, M., & Holmes, L.B. (1998). Anterior laryngeal webs and 22q11 deletions. (Letter). American Journal of Medical Genetics, 79, 152 only. Stoler, J.M., Ladoulis, M., & Holmes, L.B. (1998). Anterior laryngeal webs and 22q11 deletions. (Letter). American Journal of Medical Genetics, 79, 152 only.
go back to reference Strakowski, S.M., Butler, M.G., Cheek, J.W., Moore, W.T., Netterville, J.L., & Phillips, J.A. (1988). Familial laryngeal web in three generations with probable autosomal dominant transmission. Dysmorphology & Clinical Genetics, 2, 9-12. Strakowski, S.M., Butler, M.G., Cheek, J.W., Moore, W.T., Netterville, J.L., & Phillips, J.A. (1988). Familial laryngeal web in three generations with probable autosomal dominant transmission. Dysmorphology & Clinical Genetics, 2, 9-12.
go back to reference Temple, I.K. (1989). Stickler syndrome. Journal of Medical Genetics, 26, 119-126. Temple, I.K. (1989). Stickler syndrome. Journal of Medical Genetics, 26, 119-126.
go back to reference Thompson, M.W., McInnes, R.R., & Willard, H.F. (1991). Genetics in medicine. Philadelphia: WB Saunders Company. Thompson, M.W., McInnes, R.R., & Willard, H.F. (1991). Genetics in medicine. Philadelphia: WB Saunders Company.
go back to reference Tucker, H.M. (1983). Congenital bilateral recurrent nerve paralysis and ptosis: A new syndrome? Laryngoscope, 93, 1405-1407. Tucker, H.M. (1983). Congenital bilateral recurrent nerve paralysis and ptosis: A new syndrome? Laryngoscope, 93, 1405-1407.
go back to reference Van Lierde, K.M., Van Borsel, J., Van Cauwenberge P., & Callewaert S. (2001). Speech patterns in children with velo-cardio-facial syndrome: two case studies. Folia Phoniatrica Logopedica, 53, 213-221. Van Lierde, K.M., Van Borsel, J., Van Cauwenberge P., & Callewaert S. (2001). Speech patterns in children with velo-cardio-facial syndrome: two case studies. Folia Phoniatrica Logopedica, 53, 213-221.
go back to reference Van Staey, M., De Bie, S., Matton, M.T., e.a. (1984). Familial congenital oesophageal atresia. Human Genetics, 66, 260. Van Staey, M., De Bie, S., Matton, M.T., e.a. (1984). Familial congenital oesophageal atresia. Human Genetics, 66, 260.
go back to reference Weiss, L.S., & White, J.A. (1990). Macroglossia: a review. Journal of the Louisiana State Medical Society, 142, 13-6. Weiss, L.S., & White, J.A. (1990). Macroglossia: a review. Journal of the Louisiana State Medical Society, 142, 13-6.
go back to reference Weng, E., Mortier, G., & Graham, J. (1995). Beckwith-Wiedemann Syndrome. An update and review for the Primary Pediatrician. Clinical Pediatrics, 34, 317-326. Weng, E., Mortier, G., & Graham, J. (1995). Beckwith-Wiedemann Syndrome. An update and review for the Primary Pediatrician. Clinical Pediatrics, 34, 317-326.
go back to reference Wilkin, D.J., Mortier, G.R., Johnson, C.L., e.a. (1998). Correlation of linkage data with clinical features in eight families with Stickler syndrome. American Journal Medical Genetics, 80, 121-127. Wilkin, D.J., Mortier, G.R., Johnson, C.L., e.a. (1998). Correlation of linkage data with clinical features in eight families with Stickler syndrome. American Journal Medical Genetics, 80, 121-127.
go back to reference Zaw-Tun, H.I. (1988). Development of congenital laryngeal atresias and clefts. Annals of Otology Rhinology and Laryngology, 97, 353-358. Zaw-Tun, H.I. (1988). Development of congenital laryngeal atresias and clefts. Annals of Otology Rhinology and Laryngology, 97, 353-358.
Metagegevens
Titel
Aangeboren afwijkingen van het spraakorgaan
Auteurs
H.F.M. Peters
R. Bastiaanse
J. Van Borsel
K. Jansonius-Schultheiss
Sj. Van der Meulen
B.J.E. Mondelaers
Copyright
2014
Uitgeverij
Bohn Stafleu van Loghum
DOI
https://doi.org/10.1007/978-90-368-0782-1_5