Overview of epidemiology, genetics, birth defects, and chromosome abnormalities associated with CDH

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

Volumn 145, Issue 2, 2007, Pages 158-171

  Pober, Barbara R ^a,b,c,d  

^a HARVARD MEDICAL SCHOOL   (United States)

^b BOSTON CHILDREN S HOSPITAL   (United States)

^c MASSACHUSETTS GENERAL HOSPITAL   (United States)

^d Center for Human Genetic Research   (United States)

Author keywords

Bochdalek hernia; Chromosome abnormalities; Classification; Congenital diaphragmatic hernia; Epidemiology; Genetic syndromes; Isolated CDH; Morgagni hernia; Mortality; Multiplex families; Syndromic CDH

Indexed keywords

BIRTH DEFECT; BOCHDALEK HERNIA; CARDIOVASCULAR MALFORMATION; CHROMOSOME 8Q; CHROMOSOME ABERRATION; CHROMOSOME DELETION; CHROMOSOME REARRANGEMENT; CLINICAL FEATURE; CONFERENCE PAPER; CONGENITAL DIAPHRAGM HERNIA; DISEASE ASSOCIATION; DISEASE CLASSIFICATION; GENE LOCATION; GENETIC DISORDER; HUMAN; ISOCHROMOSOME; MEDICAL RESEARCH; MORTALITY; PREVALENCE; PRIORITY JOURNAL; TETRASOMY; TRISOMY 18; TRISOMY 21;

ABNORMALITIES; ABNORMALITIES, MULTIPLE; CARDIOVASCULAR ABNORMALITIES; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 15; FAMILY HEALTH; HERNIA, DIAPHRAGMATIC; HUMANS; META-ANALYSIS; PREVALENCE;

EID: 34249063569     PISSN: 15524868     EISSN: 15524876     Source Type: Journal    
DOI: 10.1002/ajmg.c.30126     Document Type: Conference Paper

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