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Fertility and Sterility

Volumn 86, Issue 6, 2006, Pages 1801-1802

Techniques and reasons to remain interested in the Y chromosome

(3) Noordam, Michiel J a van der Veen, Fulco a Repping, Sjoerd a

a ACADEMIC MEDICAL CENTER (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME DELETION Y; CHROMOSOME POLYMORPHISM; GENE DELETION; HUMAN; LETTER; MOLECULAR GENETICS; PREGNANCY OUTCOME; PRIORITY JOURNAL; SCREENING; SPERMATOGENESIS; Y CHROMOSOME;

ABORTION, HABITUAL; ADULT; CASE-CONTROL STUDIES; CHROMOSOMES, HUMAN, Y; GENE DELETION; GENE FREQUENCY; HUMANS; INFERTILITY, MALE; MALE; POLYMERASE CHAIN REACTION; SEX CHROMOSOME ABERRATIONS;

EID: 33751178805 PISSN: 00150282 EISSN: None Source Type: Journal
DOI: 10.1016/j.fertnstert.2006.07.1454 Document Type: Letter

Times cited : (11)

References (7)

1
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- Role of the AZFd locus in spermatogenesis
- Muslumanoglu M.H., Turgut M., Cilingir O., Can C., Ozyurek Y., and Artan S. Role of the AZFd locus in spermatogenesis. Fertil Steril 84 (2005) 519-522
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- Muslumanoglu, M.H.¹ Turgut, M.² Cilingir, O.³ Can, C.⁴ Ozyurek, Y.⁵ Artan, S.⁶

2
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- Y-chromosome microdeletions and recurrent pregnancy loss
- Dewan S., Puscheck E.E., Coulam C.B., Wilcox A.J., and Jeyendran R.S. Y-chromosome microdeletions and recurrent pregnancy loss. Fertil Steril 85 (2006) 441-445
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- Dewan, S.¹ Puscheck, E.E.² Coulam, C.B.³ Wilcox, A.J.⁴ Jeyendran, R.S.⁵

3
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- High mutation rates have driven extensive structural polymorphism among human Y chromosomes
- Repping S., van Daalen S.K., Brown L.G., Korver C.M., Lange J., Marszalek J.D., et al. High mutation rates have driven extensive structural polymorphism among human Y chromosomes. Nat Genet 38 (2006) 463-467
- (2006) Nat Genet , vol.38 , pp. 463-467
- Repping, S.¹ van Daalen, S.K.² Brown, L.G.³ Korver, C.M.⁴ Lange, J.⁵ Marszalek, J.D.⁶

4
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- EAA/EMQN best practice guidelines for molecular diagnosis of Y-chromosomal microdeletions. State of the art 2004
- Simoni M., Bakker E., and Krausz C. EAA/EMQN best practice guidelines for molecular diagnosis of Y-chromosomal microdeletions. State of the art 2004. Int J Androl 27 (2004) 240-249
- (2004) Int J Androl , vol.27 , pp. 240-249
- Simoni, M.¹ Bakker, E.² Krausz, C.³

5
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- Polymorphism for a 1.6-Mb deletion of the human Y chromosome persists through balance between recurrent mutation and haploid selection
- Repping S., Skaletsky H., Brown L., van Daalen S.K., Korver C.M., Pyntikova T., et al. Polymorphism for a 1.6-Mb deletion of the human Y chromosome persists through balance between recurrent mutation and haploid selection. Nat Genet 35 (2003) 247-251
- (2003) Nat Genet , vol.35 , pp. 247-251
- Repping, S.¹ Skaletsky, H.² Brown, L.³ van Daalen, S.K.⁴ Korver, C.M.⁵ Pyntikova, T.⁶

6
- 2642530984
- A family of human Y chromosomes has dispersed throughout northern Eurasia despite a 1.8-Mb deletion in the azoospermia factor c region
- Repping S., van Daalen S.K., Korver C.M., Brown L.G., Marszalek J.D., Gianotten J., et al. A family of human Y chromosomes has dispersed throughout northern Eurasia despite a 1.8-Mb deletion in the azoospermia factor c region. Genomics 83 (2004) 1046-1052
- (2004) Genomics , vol.83 , pp. 1046-1052
- Repping, S.¹ van Daalen, S.K.² Korver, C.M.³ Brown, L.G.⁴ Marszalek, J.D.⁵ Gianotten, J.⁶

7
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- The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes
- Skaletsky H., Kuroda-Kawaguchi T., Minx P.J., Cordum H.S., Hillier L., Brown L.G., et al. The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes. Nature 423 (2003) 825-837
- (2003) Nature , vol.423 , pp. 825-837
- Skaletsky, H.¹ Kuroda-Kawaguchi, T.² Minx, P.J.³ Cordum, H.S.⁴ Hillier, L.⁵ Brown, L.G.⁶

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.