Het syndroom van Meier-Gorlin

Tijdschrift voor Kindergeneeskunde

Volumn 67, Issue 1, 1999, Pages 32-35

  Verhallen, J T C M ^a   Van Der Lely, N ^a   Kant, S G ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0002046552     PISSN: 03767442     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (7)

1. Meier VZ, Poschiavo, Rothschild M Ein Fall von Arthrogryposis multiplex congenita kombimert mit Dysostosis mandibulofacialis (Franceschetti-Syndrom). Helv Paediatr Acta 1959;2:213-6.
2. Gorlin RJ, Cervenka J, Moller K, et al. A selected miscellany Birth Defects 1975;11:39-50.
3. Boles RG, Teebi AS, Schwartz D, et al Further delineation of the ear, patella, short stature syndrome (Meier-Gorlin syndrome). Clin Dysmorphol 1994;3:207-14
4. Cohen B, Temple IK, Symons JC, et al Microtia and short stature: a new syndrome. J Med Genet 1991;28:786-90.
5. Lacombe D, Toutain A, Gorlin RJ, et al. Clinical identification of a human equivalent to the short ear (se) murine phenotype. Ann Genet 1994;37:184-91.
6. Gorlin RJ. Microtia, absent patellae, short stature, micrognathia syndrome. J Med Genet 1992;29:516
7. Hurst JA, Winter RM, Baraitser M. Distinctive syndrome of short stature, craniosynostosis, skeletal changes and malformed ears. Am J Med Genet 1988;29:107-15.