Brief clinical report: Holoprosencephaly associated with an apparent isolated 2q37.1→2q37.3 deletion

American Journal of Medical Genetics

Volumn 100, Issue 3, 2001, Pages 179-181

  Lehman, Norman L ^a,c   Zaleski, Dianna H ^b   Sanger, Warren G ^b   Adickes, Edward D ^a  

^a CREIGHTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF NEBRASKA MEDICAL CENTER   (United States)

^c STANFORD UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

2q37 deletion; Holoprosencephaly; Lobar variant

Indexed keywords

ARTICLE; BRAIN DEVELOPMENT; CASE REPORT; CHROMOSOME 2Q; CHROMOSOME DELETION; CYTOGENETICS; FEMALE; FOREBRAIN; HOLOPROSENCEPHALY; HUMAN; HUMAN TISSUE; INFANT; PARTIAL MONOSOMY; PRIORITY JOURNAL; CHROMOSOME 2; GENETICS; KARYOTYPING; NEWBORN;

CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 2; FEMALE; HOLOPROSENCEPHALY; HUMANS; INFANT, NEWBORN; KARYOTYPING;

EID: 0035341275     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.1245     Document Type: Article

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