SCOPUS 정보 검색 플랫폼

American Journal of Human Genetics

Volumn 59, Issue 2, 1996, Pages 423-430

Allele-specific replication of 15q11-q13 loci: A diagnostic test for detection of uniparental disomy

(6) White, Lisa M a Rogan, Peter K c,e Nicholls, Robert D d Wu, Bai Lin a Korf, Bruce a Knoll, Joan H M a,b

a BOSTON CHILDREN S HOSPITAL (United States)

b BETH ISRAEL DEACONESS MEDICAL CENTER (United States)

c PENNSYLVANIA STATE UNIVERSITY (United States)

d CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE (United States)

e ALLEGHENY SINGER RESEARCH INSTITUTE (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; SMALL NUCLEAR RIBONUCLEOPROTEIN;

ARTICLE; CHROMOSOME 15Q; CHROMOSOME ANALYSIS; CHROMOSOME REPLICATION; CONTROLLED STUDY; DIAGNOSTIC TEST; DISOMY; DNA METHYLATION; DNA PROBE; FLUORESCENCE IN SITU HYBRIDIZATION; HAPPY PUPPET SYNDROME; HUMAN; HUMAN CELL; INTERPHASE; LYMPHOBLASTOID CELL; LYMPHOCYTE; METAPHASE; PRADER WILLI SYNDROME; PRIORITY JOURNAL;

ADULT; ALLELES; ANGELMAN SYNDROME; AUTOANTIGENS; CHILD; CHROMOSOMES, HUMAN, PAIR 15; DNA REPLICATION; GENOMIC IMPRINTING; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; PRADER-WILLI SYNDROME; RIBONUCLEOPROTEINS, SMALL NUCLEAR;

EID: 0029811340 PISSN: 00029297 EISSN: None Source Type: Journal
DOI: None Document Type: Article

Times cited : (37)

References (5)

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2
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- Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15
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3
- 0022462350
- Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome
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- Butler, M.G.¹ Meaney, F.J.² Palmer, C.G.³

4
- 0021094659
- Parental origin of chromosome 15 deletion in Prader-Willi syndrome
- Butler MG, Palmer CG (1983) Parental origin of chromosome 15 deletion in Prader-Willi syndrome. Lancet 1:1285-1286
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- Butler, M.G.¹ Palmer, C.G.²

5
- 0027520382
- Difference in methylation patterns within the D15S9 region of chromosome 15q11-13 in first cousins with Angelman syndrome and Prader-Willi syndrome
- Clayton-Smith J, Driscoll DJ, Waters MF, Webb T, Andrews T, Malcolm S, Pembrey ME, et al (1993) Difference in methylation patterns within the D15S9 region of chromosome 15q11-13 in first cousins with Angelman syndrome and Prader-Willi syndrome. Am J Med Genet 47:683-686
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.