Mowat-Wilson syndrome

Journal of Medical Genetics

Volumn 40, Issue 5, 2003, Pages 305-310

  Mowat, D R ^a,b   Wilson, M J ^c   Goossens, M ^d  

^a SYDNEY CHILDREN'S HOSPITAL   (Australia)

^b UNIVERSITY OF NEW SOUTH WALES   (Australia)

^c CHILDREN S HOSPITAL AT WESTMEAD   (Australia)

^d HENRI MONDOR HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT; PROTEIN ZFHX1B; UNCLASSIFIED DRUG;

CHROMOSOME 2Q; CLINICAL FEATURE; CONGENITAL HEART DISEASE; CONGENITAL MALFORMATION; CORPUS CALLOSUM AGENESIS; CRANIOFACIAL MALFORMATION; DISEASE ASSOCIATION; DISEASE SEVERITY; GENE DELETION; GENE EXPRESSION; GENE MUTATION; HETEROZYGOSITY; HIRSCHSPRUNG DISEASE; HUMAN; HYPOSPADIAS; INTELLECTUAL IMPAIRMENT; MICROCEPHALY; MOWAT WILSON SYNDROME; PHENOTYPE; PRIORITY JOURNAL; REVIEW; SEIZURE; SHORT STATURE; UROGENITAL TRACT MALFORMATION;

EID: 0038577214     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.40.5.305     Document Type: Review

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