Fryns Syndrome: A Review of the Phenotype and Diagnostic Guidelines

American Journal of Medical Genetics

Volumn 124 A, Issue 4, 2004, Pages 427-433

  Slavotinek, Anne M ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Brachytelephalangy; Congenital diaphragmatic hernia; Fryns syndrome; Pulmonary hypoplasia

Indexed keywords

AORTA ANOMALY; AUTOSOMAL RECESSIVE DISORDER; BONE MALFORMATION; BRAIN VENTRICLE DILATATION; CHROMOSOME ABERRATION; CLEFT FACE; CLINICAL FEATURE; CONGENITAL DIAPHRAGM HERNIA; CORPUS CALLOSUM AGENESIS; CRANIOFACIAL MALFORMATION; CYTOGENETICS; DIAGNOSTIC TEST; DISEASE ASSOCIATION; FRYNS SYNDROME; HETEROTOPIA; HUMAN; HYDRAMNIOS; HYDROCEPHALUS; KARYOTYPE; KIDNEY CYST; KIDNEY DYSPLASIA; LIMB MALFORMATION; LUNG HYPOPLASIA; MAJOR CLINICAL STUDY; MULTIPLE MALFORMATION SYNDROME; NAIL HYPOPLASIA; PHENOTYPIC VARIATION; PRACTICE GUIDELINE; PRIORITY JOURNAL; REVIEW; URETER DILATATION; UTERUS BICORNIS;

EID: 0942279747     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.20381     Document Type: Review

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