SCOPUS 정보 검색 플랫폼

Volumn 38, Issue 12, 2001, Pages 876-881

Maternal uniparental isodisomy 11q13→qter in a dysmorphic and mentally retarded female with partial trisomy mosaicism 11q13→qter [9]

(4) Kotzot, D a Rothlisberger B a Riegel, M a Schinzel, A a

a UNIVERSITY OF ZURICH (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ALLELE; CASE REPORT; CHROMOSOME 11Q; CHROMOSOME ANALYSIS; CROSSING OVER; FACE DYSMORPHIA; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; LETTER; MENTAL RETARDATION MALFORMATION SYNDROME; MOSAICISM; PARTIAL TRISOMY; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; TRISOMY 11Q; UNIPARENTAL DISOMY;

ADULT; ALLELES; CELLS, CULTURED; CHILD; CHROMATIDS; CHROMOSOME BREAKAGE; CHROMOSOMES, HUMAN, PAIR 11; CHROMOSOMES, HUMAN, PAIR 19; CRANIOFACIAL ABNORMALITIES; FEMALE; FIBROBLASTS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; INFANT, NEWBORN; KARYOTYPING; LYMPHOCYTES; MALE; MEIOSIS; MENTAL RETARDATION; MICROSATELLITE REPEATS; MITOSIS; MODELS, GENETIC; MOSAICISM; TRISOMY; UNIPARENTAL DISOMY;

EID: 0035662375 PISSN: 00222593 EISSN: None Source Type: Journal
DOI: None Document Type: Letter

Times cited : (5)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.