The gr/gr deletion(s): a new genetic test in male infertility?

被引：87

作者：

Giachini, C

Guarducci, E

Longepied, G

Degl'Innocenti, S

Becherini, L

Forti, G

Mitchell, MJ

Krausz, C

机构：

[1] Univ Florence, Androl Unit, Dept Clin Physiopathol, Ctr Res Transfer & Higher Educ Chron Inflammatory, I-50139 Florence, Italy

[2] Fac Med Marseille, INSERM, U491, F-13385 Marseille, France

[3] Inst Reprod Med, F-13008 Marseille, France

来源：

JOURNAL OF MEDICAL GENETICS | 2005年 / 42卷 / 06期

关键词：

D O I：

10.1136/jmg.2004.028191

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

[No abstract available]

引用

页码：497 / 502

页数：6

共 23 条

[1] DAZL polymorphisms and susceptibility to spermatogenic failure: an example of remarkable ethnic differences [J].

Becherini, L ;

Guarducci, E ;

Degl'Innocenti, S ;

Rotondi, M ;

Forti, G ;

Krausz, C .

INTERNATIONAL JOURNAL OF ANDROLOGY, 2004, 27 (06) :375-381

[2] A large AZFc deletion removes DAZ3/DAZ4 and nearby genes from men in Y haplogroup N [J].

Fernandes, S ;

Paracchini, S ;

Meyer, LH ;

Floridia, G ;

Smith, CT ;

Vogt, PH .

AMERICAN JOURNAL OF HUMAN GENETICS, 2004, 74 (01) :180-187

[3] High frequency of DAZ1/DAZ2 gene deletions in patients with severe oligozoospermia [J].

Fernandes, S ;

Huellen, K ;

Goncalves, J ;

Dukal, H ;

Zeisler, J ;

De MEyts, ER ;

Skakkebaek, NE ;

Habermann, B ;

Krause, W ;

Sousa, M ;

Barros, A ;

Vogt, PH .

MOLECULAR HUMAN REPRODUCTION, 2002, 8 (03) :286-298

[4] Prognostic value of Y deletion analysis - What is the clinical prognostic value of Y chromosome microdeletion analysis? [J].

Krausz, C ;

Quintana-Murci, L ;

McElreavey, K .

HUMAN REPRODUCTION, 2000, 15 (07) :1431-1434

[5] The Y chromosome and male fertility and infertility [J].

Krausz, C ;

Forti, G ;

McElreavey, K .

INTERNATIONAL JOURNAL OF ANDROLOGY, 2003, 26 (02) :70-75

[6]

KURODAKAWAGUCHI T, 2001, NAT GENET, V29, P79286

[7] Sequence family variant loss from the AZFc interval of the human Y chromosome, but not gene copy loss, is strongly associated with male infertility [J].

Machev, N ;

Saut, N ;

Longepied, G ;

Terriou, P ;

Navarro, A ;

Levy, N ;

Guichaoua, M ;

Metzler-Guillemain, C ;

Collignon, P ;

Frances, AM ;

Belougne, J ;

Clemente, E ;

Chiaroni, J ;

Chevillard, C ;

Durand, C ;

Ducourneau, A ;

Pech, N ;

McElreavey, K ;

Mattei, MG ;

Mitchell, MJ .

JOURNAL OF MEDICAL GENETICS, 2004, 41 (11) :814-825

[8] DIVERSE SPERMATOGENIC DEFECTS IN HUMANS CAUSED BY Y-CHROMOSOME DELETIONS ENCOMPASSING A NOVEL RNA-BINDING PROTEIN GENE [J].

REIJO, R ;

LEE, TY ;

SALO, P ;

ALAGAPPAN, R ;

BROWN, LG ;

ROSENBERG, M ;

ROZEN, S ;

JAFFE, T ;

STRAUS, D ;

HOVATTA, O ;

DELACHAPELLE, A ;

SILBER, S ;

PAGE, DC .

NATURE GENETICS, 1995, 10 (04) :383-393

[9] Recombination between palindromes P5 and P1 on the human Y chromosome causes massive deletions and spermatogenic failure [J].

Repping, S ;

Skaletsky, H ;

Lange, J ;

Silber, S ;

van der Veen, F ;

Oates, RD ;

Page, DC ;

Rozen, S .

AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) :906-922

[10] Polymorphism for a 1.6-Mb deletion of the human Y chromosome persists through balance between recurrent mutation and haploid selection [J].

Repping, S ;

Skaletsky, H ;

Brown, L ;

van Daalen, SKM ;

Korver, CM ;

Pyntikova, T ;

Kuroda-Kawaguchi, T ;

de Vries, JWA ;

Oates, RD ;

Silber, S ;

van der Veen, F ;

Page, DC ;

Rozen, S .

NATURE GENETICS, 2003, 35 (03) :247-251

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