SCOPUS 정보 검색 플랫폼

Volumn 8, Issue 11, 2000, Pages 815-819

Familial Robertsonian translocation 15;21 and rare paracentric inv(21): Unexpected re-inversion in a child with translocation trisomy 21

(4) Mau, Ulrike A a Petruch, Uwe R a Kaiser, Peter a Eggermann, Thomas b

a UNIVERSITY OF TÜBINGEN (Germany)

b RWTH AACHEN UNIVERSITY (Germany)

Author keywords

Paracentric inversion 21q; Reinversion; Translocation trisomy 21

Indexed keywords

ALLELE; ARTICLE; AUTOSOMAL INHERITANCE; CASE REPORT; CHILD; CHROMOSOME 21Q; CHROMOSOME ANALYSIS; CHROMOSOME SEGREGATION; CHROMOSOME TRANSLOCATION 15; CHROMOSOME TRANSLOCATION 21; CONTROLLED STUDY; DOWN SYNDROME; FAMILY HEALTH; GENETIC ANALYSIS; GENETIC LINKAGE; GENETIC PREDISPOSITION; HETEROZYGOTE; HUMAN; HUMAN CELL; KARYOTYPING; MALE; MEIOSIS; MOTHER; PARACENTRIC CHROMOSOME INVERSION; PRIORITY JOURNAL; ROBERTSONIAN CHROMOSOME TRANSLOCATION; SEGREGATION ANALYSIS; SUPERNUMERARY CHROMOSOME; TANDEM REPEAT; TRISOMY 21;

ADULT; CHROMOSOMES, HUMAN, PAIR 15; CHROMOSOMES, HUMAN, PAIR 21; FAMILY HEALTH; HUMANS; INFANT; INVERSION, CHROMOSOME; KARYOTYPING; MALE; MICROSATELLITE REPEATS; PEDIGREE; TRANSLOCATION, GENETIC; TRISOMY;

ROBERTSONIA;

EID: 0033724525 PISSN: 10184813 EISSN: None Source Type: Journal
DOI: 10.1038/sj.ejhg.5200544 Document Type: Article

Times cited : (2)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.