-
1
-
-
0017119580
-
Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human y chromosome long arm
-
L. Tiepolo, and O. Zuffardi Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human Y chromosome long arm Hum Genet 34 1976 119 124
-
(1976)
Hum Genet
, vol.34
, pp. 119-124
-
-
Tiepolo, L.1
Zuffardi, O.2
-
2
-
-
0026726412
-
The human y chromosome: Overlapping DNA clones spanning the euchromatic region
-
S. Foote, D. Vollrath, A. Hilton, and D.C. Page The human Y chromosome: overlapping DNA clones spanning the euchromatic region Science 258 1992 60 66
-
(1992)
Science
, vol.258
, pp. 60-66
-
-
Foote, S.1
Vollrath, D.2
Hilton, A.3
Page, D.C.4
-
3
-
-
0026756965
-
The human y chromosome: A 43-interval map based on naturally occurring deletions
-
D. Vollrath, S. Foote, A. Hilton, L.G. Brown, P. Beer-Romero, and J.S. Bogan The human Y chromosome: a 43-interval map based on naturally occurring deletions Science 258 1992 52 59
-
(1992)
Science
, vol.258
, pp. 52-59
-
-
Vollrath, D.1
Foote, S.2
Hilton, A.3
Brown, L.G.4
Beer-Romero, P.5
Bogan, J.S.6
-
4
-
-
0027715823
-
A y chromosome gene family with RNA-binding protein homology: Candidates for the azoospermia factor AZF controlling human spermatogenesis
-
K. Ma, J.D. Inglis, A. Sharkey, W.A. Bickmore, R.E. Hill, and E.J. Prosser A Y chromosome gene family with RNA-binding protein homology: candidates for the azoospermia factor AZF controlling human spermatogenesis Cell 75 1993 1287 1295
-
(1993)
Cell
, vol.75
, pp. 1287-1295
-
-
Ma, K.1
Inglis, J.D.2
Sharkey, A.3
Bickmore, W.A.4
Hill, R.E.5
Prosser, E.J.6
-
5
-
-
0029088061
-
Diverse spermatogenic defects in humans caused by y chromosome deletions encompassing a novel RNA-binding protein gene
-
R. Reijo, T.Y. Lee, P. Salo, R. Alagappan, L.G. Brown, and M. Rosenberg Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene Nat Genet 10 1995 383 393
-
(1995)
Nat Genet
, vol.10
, pp. 383-393
-
-
Reijo, R.1
Lee, T.Y.2
Salo, P.3
Alagappan, R.4
Brown, L.G.5
Rosenberg, M.6
-
6
-
-
0026726199
-
Microdeletions in interval 6 of the y chromosome of males with idiopathic sterility point to disruption of AZF, a human spermatogenesis gene
-
P. Vogt, A.C. Chandley, T.B. Hargreave, R. Keil, K. Ma, and A. Sharkey Microdeletions in interval 6 of the Y chromosome of males with idiopathic sterility point to disruption of AZF, a human spermatogenesis gene Hum Genet 89 1992 491 496
-
(1992)
Hum Genet
, vol.89
, pp. 491-496
-
-
Vogt, P.1
Chandley, A.C.2
Hargreave, T.B.3
Keil, R.4
Ma, K.5
Sharkey, A.6
-
7
-
-
0007272350
-
Human y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11
-
P.H. Vogt, A. Edelmann, S. Kirsch, O. Henegariu, P. Hirschmann, and F. Kiesewetter Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11 Hum Mol Genet 5 1996 933 943
-
(1996)
Hum Mol Genet
, vol.5
, pp. 933-943
-
-
Vogt, P.H.1
Edelmann, A.2
Kirsch, S.3
Henegariu, O.4
Hirschmann, P.5
Kiesewetter, F.6
-
8
-
-
0035014112
-
Meiotic behaviour of the sex chromosomes in three patients with sex chromosome anomalies (47, XXY, mosaic 46, XY/47, XXY and 47, XYY) assessed by fluorescence in-situ hybridization
-
J. Blanco, J. Egozcue, and F. Vidal Meiotic behaviour of the sex chromosomes in three patients with sex chromosome anomalies (47, XXY, mosaic 46, XY/47, XXY and 47, XYY) assessed by fluorescence in-situ hybridization Hum Reprod 16 2001 887 892
-
(2001)
Hum Reprod
, vol.16
, pp. 887-892
-
-
Blanco, J.1
Egozcue, J.2
Vidal, F.3
-
9
-
-
0034641881
-
Two long homologous retroviral sequence blocks in proximal Yq11 cause AZFa microdeletions as a result of intrachromosomal recombination events
-
C. Kamp, P. Hirschmann, H. Voss, K. Huellen, and P.H. Vogt Two long homologous retroviral sequence blocks in proximal Yq11 cause AZFa microdeletions as a result of intrachromosomal recombination events Hum Mol Genet 9 2000 2563 2572
-
(2000)
Hum Mol Genet
, vol.9
, pp. 2563-2572
-
-
Kamp, C.1
Hirschmann, P.2
Voss, H.3
Huellen, K.4
Vogt, P.H.5
-
10
-
-
0035184973
-
The AZFc region of the y chromosome features massive palindromes and uniform recurrent deletions in infertile men
-
T. Kuroda-Kawaguchi, H. Skaletsky, L.G. Brown, P.J. Minx, H.S. Cordum, and R.H. Waterston The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile men Nat Genet 29 2001 279 286
-
(2001)
Nat Genet
, vol.29
, pp. 279-286
-
-
Kuroda-Kawaguchi, T.1
Skaletsky, H.2
Brown, L.G.3
Minx, P.J.4
Cordum, H.S.5
Waterston, R.H.6
-
11
-
-
0036782130
-
Recombination between palindromes P5 and P1 on the human y chromosome causes massive deletions and spermatogenic failure
-
C. Sun, H. Skaletsky, J. Lange, S. Silber, F. Van Der Veen, and R.D. Oates Recombination between palindromes P5 and P1 on the human Y chromosome causes massive deletions and spermatogenic failure Am J Hum Genet 71 2002 906 922
-
(2002)
Am J Hum Genet
, vol.71
, pp. 906-922
-
-
Sun, C.1
Skaletsky, H.2
Lange, J.3
Silber, S.4
Van Der Veen, F.5
Oates, R.D.6
-
12
-
-
0034703178
-
Deletion of azoospermia factor a (AZFa) region of human y chromosome caused by recombination between HERV15 proviruses
-
C. Sun, H. Skaletsky, S. Rozen, J. Gromoll, E. Nieschlag, and R. Oates Deletion of azoospermia factor a (AZFa) region of human Y chromosome caused by recombination between HERV15 proviruses Hum Mol Genet 9 2000 2291 2296
-
(2000)
Hum Mol Genet
, vol.9
, pp. 2291-2296
-
-
Sun, C.1
Skaletsky, H.2
Rozen, S.3
Gromoll, J.4
Nieschlag, E.5
Oates, R.6
-
13
-
-
0141813754
-
Idiopathic cases of male infertility from a region in India show low incidence of Y-chromosome microdeletion
-
R. Ambasudhan, K. Singh, J.K. Agarwal, S.K. Singh, A. Khanna, and R.K. Sah Idiopathic cases of male infertility from a region in India show low incidence of Y-chromosome microdeletion J Biosci 28 2003 605 612
-
(2003)
J Biosci
, vol.28
, pp. 605-612
-
-
Ambasudhan, R.1
Singh, K.2
Agarwal, J.K.3
Singh, S.K.4
Khanna, A.5
Sah, R.K.6
-
14
-
-
33947546526
-
Molecular and clinical characterization of y chromosome microdeletions in infertile men: A 10-year experience in Italy
-
A. Ferlin, B. Arredi, E. Speltra, C. Cazzadore, R. Selice, and A. Garolla Molecular and clinical characterization of Y chromosome microdeletions in infertile men: a 10-year experience in Italy J Clin Endocrinol Metab 92 2007 762 770
-
(2007)
J Clin Endocrinol Metab
, vol.92
, pp. 762-770
-
-
Ferlin, A.1
Arredi, B.2
Speltra, E.3
Cazzadore, C.4
Selice, R.5
Garolla, A.6
-
15
-
-
0036712133
-
Natural transmission of a partial AZFb deletion of the y chromosome over three generations: Case report
-
C. Rolf, J. Gromoll, M. Simoni, and E. Nieschlag Natural transmission of a partial AZFb deletion of the Y chromosome over three generations: case report Hum Reprod 17 2002 2267 2271
-
(2002)
Hum Reprod
, vol.17
, pp. 2267-2271
-
-
Rolf, C.1
Gromoll, J.2
Simoni, M.3
Nieschlag, E.4
-
16
-
-
33749507234
-
Natural transmission of AZFb Y-chromosomal microdeletion from father to his three sons
-
H. Samli, M. Murat Samli, and M. Solak Natural transmission of AZFb Y-chromosomal microdeletion from father to his three sons Arch Androl 52 2006 423 426
-
(2006)
Arch Androl
, vol.52
, pp. 423-426
-
-
Samli, H.1
Murat Samli, M.2
Solak, M.3
-
17
-
-
0037967242
-
The male-specific region of the human y chromosome is a mosaic of discrete sequence classes
-
H. Skaletsky, T. Kuroda-Kawaguchi, P.J. Minx, H.S. Cordum, L. Hillier, and L.G. Brown 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
-
18
-
-
0036178949
-
A nomenclature system for the tree of human Y-chromosomal binary haplogroups
-
A nomenclature system for the tree of human Y-chromosomal binary haplogroups Genome Res 12 2002 339 348
-
(2002)
Genome Res
, vol.12
, pp. 339-348
-
-
-
19
-
-
0242298320
-
Polymorphism for a 1.6-Mb deletion of the human y chromosome persists through balance between recurrent mutation and haploid selection
-
S. Repping, H. Skaletsky, L. Brown, S.K. van Daalen, C.M. Korver, and T. Pyntikova 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
-
20
-
-
0345742509
-
A large AZFc deletion removes DAZ3/DAZ4 and nearby genes from men in y haplogroup N
-
S. Fernandes, S. Paracchini, L.H. Meyer, G. Floridia, C. Tyler-Smith, and P.H. Vogt A large AZFc deletion removes DAZ3/DAZ4 and nearby genes from men in Y haplogroup N Am J Hum Genet 74 2004 180 187
-
(2004)
Am J Hum Genet
, vol.74
, pp. 180-187
-
-
Fernandes, S.1
Paracchini, S.2
Meyer, L.H.3
Floridia, G.4
Tyler-Smith, C.5
Vogt, P.H.6
-
21
-
-
2642530984
-
A family of human y chromosomes has dispersed throughout northern Eurasia despite a 1.8-Mb deletion in the azoospermia factor c region
-
S. Repping, S.K. van Daalen, C.M. Korver, L.G. Brown, J.D. Marszalek, and J. Gianotten 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
-
23
-
-
0024340871
-
Radioimmunoassay of testosterone not bound to sex-steroid-binding protein in plasma
-
H. Dechaud, H. Lejeune, M. Garoscio-Cholet, R. Mallein, and M. Pugeat Radioimmunoassay of testosterone not bound to sex-steroid-binding protein in plasma Clin Chem 35 1989 1609 1614
-
(1989)
Clin Chem
, vol.35
, pp. 1609-1614
-
-
Dechaud, H.1
Lejeune, H.2
Garoscio-Cholet, M.3
Mallein, R.4
Pugeat, M.5
-
24
-
-
0031024316
-
Screening for deletions of the y chromosome involving the DAZ (Deleted in AZoospermia) gene in azoospermia and severe oligozoospermia
-
M. Simoni, J. Gromoll, B. Dworniczak, C. Rolf, K. Abshagen, and A. Kamischke Screening for deletions of the Y chromosome involving the DAZ (Deleted in AZoospermia) gene in azoospermia and severe oligozoospermia Fertil Steril 67 1997 542 547
-
(1997)
Fertil Steril
, vol.67
, pp. 542-547
-
-
Simoni, M.1
Gromoll, J.2
Dworniczak, B.3
Rolf, C.4
Abshagen, K.5
Kamischke, A.6
-
25
-
-
0036901653
-
Clinical relevance of partial AZFc deletions
-
J.W. de Vries, S. Repping, S.K. van Daalen, C.M. Korver, N.J. Leschot, and F. van der Veen Clinical relevance of partial AZFc deletions Fertil Steril 78 2002 1209 1214
-
(2002)
Fertil Steril
, vol.78
, pp. 1209-1214
-
-
De Vries, J.W.1
Repping, S.2
Van Daalen, S.K.3
Korver, C.M.4
Leschot, N.J.5
Van Der Veen, F.6
-
26
-
-
18244410193
-
High frequency of DAZ1/DAZ2 gene deletions in patients with severe oligozoospermia
-
S. Fernandes, K. Huellen, J. Goncalves, H. Dukal, J. Zeisler, and E. Rajpert De Meyts High frequency of DAZ1/DAZ2 gene deletions in patients with severe oligozoospermia Mol Hum Reprod 8 2002 286 298
-
(2002)
Mol Hum Reprod
, vol.8
, pp. 286-298
-
-
Fernandes, S.1
Huellen, K.2
Goncalves, J.3
Dukal, H.4
Zeisler, J.5
Rajpert De Meyts, E.6
-
27
-
-
0033032375
-
The candidate spermatogenesis gene RBMY has a homologue on the human X chromosome
-
M.L. Delbridge, P.A. Lingenfelter, C.M. Disteche, and J.A. Graves The candidate spermatogenesis gene RBMY has a homologue on the human X chromosome Nat Genet 22 1999 223 224
-
(1999)
Nat Genet
, vol.22
, pp. 223-224
-
-
Delbridge, M.L.1
Lingenfelter, P.A.2
Disteche, C.M.3
Graves, J.A.4
-
28
-
-
43049114970
-
Identification of new breakpoints in AZFb and AZFc
-
P. Costa, R. Goncalves, C. Ferras, S. Fernandes, A.T. Fernandes, and M. Sousa Identification of new breakpoints in AZFb and AZFc Mol Hum Reprod 14 2008 251 258
-
(2008)
Mol Hum Reprod
, vol.14
, pp. 251-258
-
-
Costa, P.1
Goncalves, R.2
Ferras, C.3
Fernandes, S.4
Fernandes, A.T.5
Sousa, M.6
-
29
-
-
4143100211
-
Are sequence family variants useful for identifying deletions in the human y chromosome?
-
S. Repping, C.M. Korver, R.D. Oates, S. Silber, F. van der Veen, and D.C. Page Are sequence family variants useful for identifying deletions in the human Y chromosome? Am J Hum Genet 75 2004 514 517 author reply, 517-9
-
(2004)
Am J Hum Genet
, vol.75
, pp. 514-517
-
-
Repping, S.1
Korver, C.M.2
Oates, R.D.3
Silber, S.4
Van Der Veen, F.5
Page, D.C.6
|