SCOPUS 정보 검색 플랫폼

Volumn 17, Issue 3, 2002, Pages 133-136

First case of trisomy 13 plus mosaic trisomy 1q

(9) Liehr, Thomas a,d Schmidt, Matthias b Starke, Heike a Ziegler, Monika a Kittner, Gabriele a Heller, Anita a Rubtsov, Nikolai a,c Trifonov, Vladimir a,c Claussen, Uwe a

a Institute of Human Genetics and Anthropology (Germany)

b Central Clinic gGmbH (Germany)

c INSTITUTE OF CYTOLOGY AND GENETICS (Russian Federation)

d Institut fur Humangenetik und Anthropologie (Germany)

Author keywords

Chromosomal rearrangement; Sonographic abnormalities; Trisomy 13 plus mosaic trisomy 1q

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHROMOSOME 1Q; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME BREAKAGE; CHROMOSOME HIGH RESOLUTION BANDING ANALYSIS; CLINICAL FEATURE; DISEASE COURSE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; KARYOTYPE; METAPHASE; MISSED ABORTION; PARTIAL TRISOMY; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; TRISOMY; TRISOMY 13; TRISOMY 1Q;

ABORTION, MISSED; ADULT; CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 1; CHROMOSOMES, HUMAN, PAIR 13; FEMALE; HUMANS; KARYOTYPING; MALE; MATERNAL AGE; MOSAICISM; PREGNANCY; PREGNANCY, HIGH-RISK; PRENATAL DIAGNOSIS; TRISOMY; ULTRASONOGRAPHY, PRENATAL;

EID: 0036206609 PISSN: 10153837 EISSN: None Source Type: Journal
DOI: 10.1159/000048025 Document Type: Article

Times cited : (7)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.