22q13 Deletion Syndrome: An Update and Review for the Primary Pediatrician

Clinical Pediatrics

Volumn 43, Issue 1, 2004, Pages 43-53

  Havens, Joaquim M ^a   Visootsak, Jeannie ^b   Phelan, Mary C ^c   Graham Jr , John M ^b,d  

^a HARVARD MEDICAL SCHOOL   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c TC Thompson Children's Hospital   (United States)

^d CEDARS SINAI MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHILD; CHILD BEHAVIOR; CHROMOSOME 22Q; CHROMOSOME DELETION; CHROMOSOME DELETION 22; CLINICAL FEATURE; DEVELOPMENTAL DISORDER; FAMILY; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC ANALYSIS; GENETIC PROCEDURES; HUMAN; MENTAL DEFICIENCY; PEDIATRICIAN; PRIMARY MEDICAL CARE; REVIEW;

CHILD; CHROMOSOME DELETION; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 22; CRANIOFACIAL ABNORMALITIES; DEVELOPMENTAL DISABILITIES; HUMANS; PRIMARY HEALTH CARE; SYNDROME;

EID: 1642458249     PISSN: 00099228     EISSN: None     Source Type: Journal    
DOI: 10.1177/000992280404300106     Document Type: Review

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