Meier-Gorlin syndrome: The adult phenotype [3]

Clinical Dysmorphology

Volumn 7, Issue 3, 1998, Pages 231-232

  Fryns, J P ^a  

^a CENTER FOR HUMAN GENETICS   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; BONE MALFORMATION; CASE REPORT; EAR MALFORMATION; FACE DYSMORPHIA; FEMALE; GROWTH RETARDATION; HUMAN; LETTER; MALE; MANDIBLE HYPOPLASIA; MAXILLA HYPOPLASIA; PHENOTYPE; PRIORITY JOURNAL; SHORT STATURE; SYNDROME;

ABNORMALITIES, MULTIPLE; BODY HEIGHT; DWARFISM; EAR; FACE; FACIES; FEMALE; HUMANS; MALE; MANDIBLE; MIDDLE AGED; PHENOTYPE; SYNDROME;

EID: 0031846299     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-199807000-00016     Document Type: Letter

References (2)

1. Boles RG, Teebi AS, Schwartz D, Harper JF (1994). Further delineation of the ear, patella, short stature syndrome (Meier-Gorlin syndrome). Clin Dysmorphol 3:207-214.
2. Gorlin RJ (1992). Microtia, absent patellae, short stature, micrognathia syndrome. J Med Genet 29:516-517.