Fraser syndrome and cryptophthalmos: Review of the diagnostic criteria and evidence for phenotypic modules in complex malformation syndromes

Journal of Medical Genetics

Volumn 39, Issue 9, 2002, Pages 623-633

  Slavotinek, A M ^a   Tifft, C J ^b  

^a NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^b CHILDREN'S NATIONAL MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AMBIGUITY; ANUS ATRESIA; ARTICLE; CHILD; CHOANA ATRESIA; CLINICAL FEATURE; CONGENITAL DISORDER; CONSANGUINITY; CONTROLLED STUDY; CRYPTOPHTHALMOS; DIAGNOSTIC VALUE; DISEASE ASSOCIATION; DNA MODIFICATION; EAR MALFORMATION; FEMALE; FRASER SYNDROME; GENITAL SYSTEM; HUMAN; INFANT; KIDNEY AGENESIS; MAJOR CLINICAL STUDY; MALE; MALFORMATION SYNDROME; NEWBORN; PHENOTYPE; PRIORITY JOURNAL; PUBLICATION; SYNDACTYLY; SYNDROME DELINEATION; UTERUS MALFORMATION; VALIDATION PROCESS;

EID: 0036712853     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.39.9.623     Document Type: Article

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