Developmental field defects: Coming together of associations and sequences during blastogenesis

American Journal of Medical Genetics

Volumn 110, Issue 4, 2002, Pages 320-323

  Hersh, Joseph H ^a,e   Angle, Brad ^a   Fox, Terry L ^b   Barth, Rolf F ^c   Bendon, Robert W ^d   Gowans, Gordon ^a  

^a University of Louisville School of Medicine   (United States)

^b NATIONWIDE CHILDREN S HOSPITAL   (United States)

^c OHIO STATE UNIVERSITY   (United States)

^d KOSAIR CHILDREN'S HOSPITAL   (United States)

^e UNIVERSITY OF LOUISVILLE SCHOOL OF MEDICINE   (United States)

Author keywords

Blastogenesis; Developmental field defects; Holoprosencephaly

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 18; CHROMOSOME ABERRATION; CHROMOSOME DELETION; CLINICAL FEATURE; DEVELOPMENT FIELD; DEVELOPMENTAL DISORDER; EMBRYO DEVELOPMENT; FETUS; HOLOPROSENCEPHALY; HUMAN; INFANT; LYMPHOCYTE TRANSFORMATION; MALE; PATHOGENESIS; PRIORITY JOURNAL;

ABNORMALITIES, MULTIPLE; ANUS, IMPERFORATE; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 18; ECTROMELIA; ENCEPHALOCELE; FATAL OUTCOME; FETAL DISEASES; HEART DEFECTS, CONGENITAL; HOLOPROSENCEPHALY; HUMANS; INFANT, NEWBORN; KIDNEY; MALE;

GENETTA;

EID: 0037100086     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.10429     Document Type: Article

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