Denys-Drash syndrome and congenital diaphragmatic hernia: Another case with the 1097G > A(Arg366His) mutation

American Journal of Medical Genetics, Part A

Volumn 146, Issue 4, 2008, Pages 496-499

  Antonius, Timothy ^a   Van Bon, Bregje ^a   Eggink, Alex ^a   Van Der Burgt, Ineke ^a   Noordam, Kees ^a   Van Heijst, Arno ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

Arg366his; Chromosome 11p13; Congenital diaphragmatic hernia; Denys Drash syndrome; WT1

Indexed keywords

ARGININE; DNA; HISTIDINE; WT1 PROTEIN;

ARTICLE; CASE REPORT; CLINICAL FEATURE; CONGENITAL DIAPHRAGM HERNIA; DENYS DRASH SYNDROME; DIAPHRAGM; GENE; GENE MUTATION; HUMAN; LUNG DEVELOPMENT; LUNG HYPOPLASIA; NEWBORN; PRIORITY JOURNAL; PULMONARY HYPERTENSION; SYNDROME DELINEATION; WT1 GENE;

ARGININE; DENYS-DRASH SYNDROME; FATAL OUTCOME; FEMALE; GENES, WILMS TUMOR; HERNIA, DIAPHRAGMATIC; HISTIDINE; HUMANS; INFANT, NEWBORN; MALE; POINT MUTATION;

EID: 38949218052     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.32168     Document Type: Article

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