Scanning for telomeric deletions and duplications and uniparental disomy using genetic markers in 120 children with malformations

Human Genetics

Volumn 109, Issue 3, 2001, Pages 311-318

  Rosenberg, M J ^a   Killoran, C ^a   Dziadzio, L ^a   Chang, S ^a   Stone, D L ^a   Meck, J ^a   Aughton, D ^a   Bird, L M ^a   Bodurtha, J ^a   Cassidy, S B ^a   Graham, J M ^a   Grix, A ^a   Guttmacher, A E ^a   Hudgins, L ^a   Kozma, C ^a   Michaelis, R C ^a   Pauli, R ^a   Peters, K F ^a   Rosenbaum, K N ^a   Tifft, C J ^a   Wargowski, D ^a   Williams, M S ^a   Biesecker, L G ^a   more..

^a NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHILD; CHROMOSOME 7Q; CHROMOSOME 9P; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME ARM; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CHROMOSOME SIZE; CHROMOSOME VARIANT; COHORT ANALYSIS; CONGENITAL MALFORMATION; CYTOGENETICS; GENETIC MARKER; GENETIC SCREENING; GENOTYPE; GROWTH RETARDATION; HUMAN; MAJOR CLINICAL STUDY; MENTAL DEFICIENCY; PRIORITY JOURNAL; SCREENING TEST; SENSITIVITY AND SPECIFICITY; SHORT TANDEM REPEAT POLYMORPHISM; STATISTICS; TANDEM REPEAT; TELOMERE; UNIPARENTAL DISOMY;

ABNORMALITIES, MULTIPLE; ANEUPLOIDY; CHILD; CHROMOSOME ABERRATIONS; CHROMOSOME DELETION; FEMALE; GENETIC MARKERS; GROWTH DISORDERS; HUMANS; MALE; MENTAL RETARDATION; POLYMORPHISM, GENETIC; TANDEM REPEAT SEQUENCES; TELOMERE;

EID: 0034805155     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390100559     Document Type: Article

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