Clinical outcomes of four patients with microdeletion in the long arm of chromosome 2

American Journal of Medical Genetics

Volumn 78, Issue 1, 1998, Pages 36-43

  McMilin, Kenneth D ^a   Reiss, Jacob A ^b   Brown, Michael G ^a   Black, Mary H ^a   Buckmaster, Deborah A ^a   Durum, Connie T ^a   Gunter, Kristine A ^a   Lawce, Helen J ^a   Berry, Toby L ^b   Lamb, Olivia A ^b   Olson, Cathy L ^b   Weeks, Francoise F ^b   Yoshitomi, Marvin J ^b   Jacky, Peter B ^b   Olson, Susan B ^a   Magenis, R Ellen ^a,c  

^a OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

^b KAISER PERMANENTE   (United States)

^c OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

Author keywords

Chromosomal deletion; Human chromosome 2; Interstitial deletion; Mental retardation; Seizure disorder

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHILD; CHROMOSOME 2Q; CHROMOSOME DELETION; CHROMOSOME HIGH RESOLUTION BANDING ANALYSIS; CYTOGENETICS; FOLLOW UP; GENE LOCATION; GENOME IMPRINTING; HUMAN; KARYOTYPE; MENTAL DEFICIENCY; MONOSOMY; NEWBORN; OUTCOMES RESEARCH; PRIORITY JOURNAL; SEIZURE;

ADULT; CHILD; CHROMOSOME ABERRATIONS; CHROMOSOME DELETION; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 2; FEMALE; FOLLOW-UP STUDIES; HUMANS; MALE; MENTAL RETARDATION; SEIZURES;

GENETTA;

EID: 0031863823     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19980616)78:1<36::AID-AJMG8>3.0.CO;2-J     Document Type: Article

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