Single gene disorders associated with congenital diaphragmatic hernia

American Journal of Medical Genetics, Part C: Seminars in Medical Genetics

Volumn 145, Issue 2, 2007, Pages 172-183

  Slavotinek, Anne M ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

CDH; Congenital diaphragmatic hernia; Fryns syndrome; Syndrome

Indexed keywords

CLINICAL FEATURE; CONFERENCE PAPER; CONGENITAL DIAPHRAGM HERNIA; CONGENITAL MALFORMATION; CRANIOFRONTONASAL SYNDROME; DE LANGE SYNDROME; DENYS DRASH SYNDROME; DISEASE ASSOCIATION; EMBRYO DEVELOPMENT; EXON; GENE ISOLATION; GENE MUTATION; GENETIC DISORDER; GENOTYPE PHENOTYPE CORRELATION; HEREDITY; HOMOZYGOSITY; HUMAN; JARCHO LEVIN SYNDROME; MARFAN SYNDROME; MESOTHELIUM; MORTALITY; PATHOGENESIS; PRACTICE GUIDELINE; PRIORITY JOURNAL; SIMPSON GOLABI BEHMEL SYNDROME;

ANIMALS; CHROMOSOME ABERRATIONS; EPHRIN-B1; GENES, WILMS TUMOR; GENETIC DISEASES, X-LINKED; HERNIA, DIAPHRAGMATIC; HUMANS; MALE; MICE; MICE, MUTANT STRAINS; SYNDROME;

EID: 34249037677     PISSN: 15524868     EISSN: 15524876     Source Type: Journal    
DOI: 10.1002/ajmg.c.30125     Document Type: Conference Paper

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