Ichthyosis-characteristic appearance-mental retardation syndrome with distinct histological skin abnormalities

American Journal of Medical Genetics

Volumn 61, Issue 2, 1996, Pages 127-130

  Devriendt, Koenraad ^a   Van Den Oord, Joost ^a   De Vos, Rita ^a   Van Den Berghe, Herman ^a   Fryns, Jean Pierre ^a,b  

^a UNIVERSITY HOSPITALS LEUVEN   (Belgium)

^b CENTER FOR HUMAN GENETICS   (Belgium)

Author keywords

cleft palate; ichthyosis; megalocornea; multiple congenital anomalies

Indexed keywords

KERATOHYALIN;

ARTICLE; CASE REPORT; CONSANGUINEOUS MARRIAGE; CRANIOFACIAL MALFORMATION; GRANULAR CELL; HUMAN; ICHTHYOSIS; MALE; MENTAL DEFICIENCY; PRESCHOOL CHILD; PRIORITY JOURNAL; SKIN BIOPSY;

ABNORMALITIES, MULTIPLE; CHILD, PRESCHOOL; CLEFT PALATE; HUMANS; ICHTHYOSIS; MALE; MENTAL RETARDATION; SKIN; SKIN ABNORMALITIES; SYNDROME;

EID: 0030066156     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19960111)61:2<127::AID-AJMG4>3.0.CO;2-U     Document Type: Article

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