Syndrome of gingival hypertrophy, hirsutism, mental retardation and brachymetacarpia in two sisters: Specific entity or variant of a described condition?

American Journal of Medical Genetics

Volumn 95, Issue 3, 2000, Pages 241-246

  Göhlich Ratmann, Gudrun ^a   Lackner, Anja ^a   Schaper, J ^b   Voit, T ^a   Gillessen Kaesbach, Gabriele ^b  

^a UNIVERSITY OF DUISBURG ESSEN   (Germany)

^b UNIVERSITY HOSPITAL ESSEN   (Germany)

Author keywords

Developmental delay; Gingival fibromatosis; Hypertrichosis; Short metacarpals

Indexed keywords

ARTICLE; BRACHYMETACARPY; CASE REPORT; CLINICAL FEATURE; CONGENITAL HYPOTHYROIDISM; EAR MALFORMATION; EPILEPSY; FALLOT TETRALOGY; FAMILIAL INCIDENCE; FEMALE; GENETIC VARIABILITY; GINGIVA HYPERTROPHY; HIRSUTISM; HUMAN; LEBANON; MENTAL DEFICIENCY; MENTAL RETARDATION MALFORMATION SYNDROME; NOSE MALFORMATION; PRIORITY JOURNAL; SCHOOL CHILD; SIBLING; URETER OBSTRUCTION;

EID: 0034722844     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/1096-8628(20001127)95:3<241::AID-AJMG11>3.3.CO;2-E     Document Type: Article

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