SCOPUS 정보 검색 플랫폼

Volumn 20, Issue 11, 2000, Pages 914-916

Retrospective diagnosis of trisomy 15 in formalin-fixed, paraffin-embedded placental tissue in a newborn girl with Prader-Willi syndrome

(4) Walczak, Claudia a Enders, Herbert a Grissinger, Klaus a Dufke, Andreas a,b

a UNIVERSITY OF TÜBINGEN (Germany)

b Abteilung Molekulare Genetik (Germany)

Author keywords

CPM trisomy 15; Prader Willi syndrome; UPD15

Indexed keywords

MICROSATELLITE DNA;

ARTICLE; CASE REPORT; CHROMOSOME 15; CHROMOSOME 15Q; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CLINICAL FEATURE; DISEASE ASSOCIATION; DISEASE COURSE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; KARYOTYPE; NEWBORN; PLACENTA; PRADER WILLI SYNDROME; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RETROSPECTIVE STUDY; TRISOMY; TRISOMY 15; UNIPARENTAL DISOMY;

ADULT; AMNIOCENTESIS; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 15; FEMALE; FORMALDEHYDE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT, NEWBORN; KARYOTYPING; MATERNAL AGE; MICROSATELLITE REPEATS; MOSAICISM; PARAFFIN EMBEDDING; PLACENTA; PRADER-WILLI SYNDROME; PREGNANCY; PREGNANCY, HIGH-RISK; RETROSPECTIVE STUDIES; TRISOMY;

EID: 0033652236 PISSN: 01973851 EISSN: None Source Type: Journal
DOI: 10.1002/1097-0223(200011)20:11<914::AID-PD939>3.0.CO;2-6 Document Type: Article

Times cited : (4)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.