-
1
-
-
0038465808
-
The problem of complete Y-linkage in man
-
C. Stern The problem of complete Y-linkage in man Am. J. Hum. Genet. 9 1957 147 166
-
(1957)
Am. J. Hum. Genet.
, vol.9
, pp. 147-166
-
-
Stern, C.1
-
2
-
-
10044236413
-
Molecular evidence for absence of Y-linkage of the hairy ears trait
-
A.C. Lee, A. Kamalam, S.M. Adams, and M.A. Jobling Molecular evidence for absence of Y-linkage of the hairy ears trait Eur. J. Hum. Genet. 12 2004 1077 1079
-
(2004)
Eur. J. Hum. Genet.
, vol.12
, pp. 1077-1079
-
-
Lee, A.C.1
Kamalam, A.2
Adams, S.M.3
Jobling, M.A.4
-
3
-
-
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, L.G. Brown, S. Repping, T. Pyntikova, J. Ali, and T. Bieri 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
Repping, S.7
Pyntikova, T.8
Ali, J.9
Bieri, T.10
-
4
-
-
33847253056
-
Structural variation on the short arm of the human y chromosome: Recurrent multigene deletions encompassing Amelogenin y
-
M.A. Jobling, I.C. Lo, D.J. Turner, G.R. Bowden, A.C. Lee, Y. Xue, D. Carvalho-Silva, M.E. Hurles, S.M. Adams, and Y.M. Chang Structural variation on the short arm of the human Y chromosome: Recurrent multigene deletions encompassing Amelogenin Y Hum. Mol. Genet. 16 2007 307 316
-
(2007)
Hum. Mol. Genet.
, vol.16
, pp. 307-316
-
-
Jobling, M.A.1
Lo, I.C.2
Turner, D.J.3
Bowden, G.R.4
Lee, A.C.5
Xue, Y.6
Carvalho-Silva, D.7
Hurles, M.E.8
Adams, S.M.9
Chang, Y.M.10
-
5
-
-
2142808110
-
2003 Curt Stern Award address. on low expectation exceeded: Or, the genomic salvation of the y chromosome
-
D.C. Page 2003 Curt Stern Award address. On low expectation exceeded: Or, the genomic salvation of the Y chromosome Am. J. Hum. Genet. 74 2004 399 402
-
(2004)
Am. J. Hum. Genet.
, vol.74
, pp. 399-402
-
-
Page, D.C.1
-
6
-
-
19444372677
-
Y-linked inheritance of non-syndromic hearing impairment in a large Chinese family
-
Q.J. Wang, C.Y. Lu, N. Li, S.Q. Rao, Y.B. Shi, D.Y. Han, X. Li, J.Y. Cao, L.M. Yu, and Q.Z. Li Y-linked inheritance of non-syndromic hearing impairment in a large Chinese family J. Med. Genet. 41 2004 e80
-
(2004)
J. Med. Genet.
, vol.41
, pp. 80
-
-
Wang, Q.J.1
Lu, C.Y.2
Li, N.3
Rao, S.Q.4
Shi, Y.B.5
Han, D.Y.6
Li, X.7
Cao, J.Y.8
Yu, L.M.9
Li, Q.Z.10
-
7
-
-
67650322069
-
The large Chinese family with Y-linked hearing loss revisited: Clinical investigation
-
Q.J. Wang, S.Q. Rao, Y.L. Zhao, Q.J. Liu, L. Zong, M.K. Han, D.Y. Han, and W.Y. Yang The large Chinese family with Y-linked hearing loss revisited: Clinical investigation Acta Otolaryngol. 129 2009 638 643
-
(2009)
Acta Otolaryngol.
, vol.129
, pp. 638-643
-
-
Wang, Q.J.1
Rao, S.Q.2
Zhao, Y.L.3
Liu, Q.J.4
Zong, L.5
Han, M.K.6
Han, D.Y.7
Yang, W.Y.8
-
8
-
-
69949140292
-
Human y chromosome base-substitution mutation rate measured by direct sequencing in a deep-rooting pedigree
-
Asan
-
Y. Xue, Q. Wang, Q. Long, B.L. Ng, H. Swerdlow, J. Burton, C. Skuce, R. Taylor, Z. Abdellah, Y. Zhao Asan Human Y chromosome base-substitution mutation rate measured by direct sequencing in a deep-rooting pedigree Curr. Biol. 19 2009 1453 1457
-
(2009)
Curr. Biol.
, vol.19
, pp. 1453-1457
-
-
Xue, Y.1
Wang, Q.2
Long, Q.3
Ng, B.L.4
Swerdlow, H.5
Burton, J.6
Skuce, C.7
Taylor, R.8
Abdellah, Z.9
Zhao, Y.10
-
9
-
-
0042766533
-
The human y chromosome: An evolutionary marker comes of age
-
M.A. Jobling, and C. Tyler-Smith The human Y chromosome: An evolutionary marker comes of age Nat. Rev. Genet. 4 2003 598 612
-
(2003)
Nat. Rev. Genet.
, vol.4
, pp. 598-612
-
-
Jobling, M.A.1
Tyler-Smith, C.2
-
10
-
-
0034764307
-
SSAHA: A fast search method for large DNA databases
-
Z. Ning, A.J. Cox, and J.C. Mullikin SSAHA: A fast search method for large DNA databases Genome Res. 11 2001 1725 1729
-
(2001)
Genome Res.
, vol.11
, pp. 1725-1729
-
-
Ning, Z.1
Cox, A.J.2
Mullikin, J.C.3
-
11
-
-
35348988679
-
Paired-end mapping reveals extensive structural variation in the human genome
-
J.O. Korbel, A.E. Urban, J.P. Affourtit, B. Godwin, F. Grubert, J.F. Simons, P.M. Kim, D. Palejev, N.J. Carriero, and L. Du Paired-end mapping reveals extensive structural variation in the human genome Science 318 2007 420 426
-
(2007)
Science
, vol.318
, pp. 420-426
-
-
Korbel, J.O.1
Urban, A.E.2
Affourtit, J.P.3
Godwin, B.4
Grubert, F.5
Simons, J.F.6
Kim, P.M.7
Palejev, D.8
Carriero, N.J.9
Du, L.10
-
12
-
-
36448931584
-
High-efficiency thermal asymmetric interlaced PCR for amplification of unknown flanking sequences
-
652, 654 passim
-
Y.-G. Liu, and Y. Chen High-efficiency thermal asymmetric interlaced PCR for amplification of unknown flanking sequences Biotechniques 43 2007 649 650 652, 654 passim
-
(2007)
Biotechniques
, vol.43
, pp. 649-650
-
-
Liu, Y.-G.1
Chen, Y.2
-
13
-
-
59249105978
-
A microhomology-mediated break-induced replication model for the origin of human copy number variation
-
P.J. Hastings, G. Ira, and J.R. Lupski A microhomology-mediated break-induced replication model for the origin of human copy number variation PLoS Genet. 5 2009 e1000327
-
(2009)
PLoS Genet.
, vol.5
, pp. 1000327
-
-
Hastings, P.J.1
Ira, G.2
Lupski, J.R.3
-
14
-
-
0027957582
-
Highly informative compound haplotypes for the human y chromosome
-
N. Mathias, M. Bayés, and C. Tyler-Smith Highly informative compound haplotypes for the human Y chromosome Hum. Mol. Genet. 3 1994 115 123
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 115-123
-
-
Mathias, N.1
Bayés, M.2
Tyler-Smith, C.3
-
15
-
-
34248631398
-
TSPY gene copy number as a potential new risk factor for male infertility
-
R. Vodicka, R. Vrtel, L. Dusek, A.R. Singh, K. Krizova, V. Svacinova, V. Horinova, J. Dostal, I. Oborna, and J. Brezinova TSPY gene copy number as a potential new risk factor for male infertility Reprod. Biomed. Online 14 2007 579 587
-
(2007)
Reprod. Biomed. Online
, vol.14
, pp. 579-587
-
-
Vodicka, R.1
Vrtel, R.2
Dusek, L.3
Singh, A.R.4
Krizova, K.5
Svacinova, V.6
Horinova, V.7
Dostal, J.8
Oborna, I.9
Brezinova, J.10
-
16
-
-
0344874051
-
DFNA49, a novel locus for autosomal dominant non-syndromic hearing loss, maps proximal to DFNA7/DFNM1 region on chromosome 1q21-q23
-
M.A. Moreno-Pelayo, S. Modamio-Høybjør, A. Mencía, I. del Castillo, S. Chardenoux, M. Fernández-Burriel, M. Lathrop, C. Petit, and F. Moreno DFNA49, a novel locus for autosomal dominant non-syndromic hearing loss, maps proximal to DFNA7/DFNM1 region on chromosome 1q21-q23 J. Med. Genet. 40 2003 832 836
-
(2003)
J. Med. Genet.
, vol.40
, pp. 832-836
-
-
Moreno-Pelayo, M.A.1
Modamio-Høybjør, S.2
Mencía, A.3
Del Castillo, I.4
Chardenoux, S.5
Fernández-Burriel, M.6
Lathrop, M.7
Petit, C.8
Moreno, F.9
-
17
-
-
78650989309
-
The audiological characteristics of a hereditary Y-linked hearing loss in a Chinese ethnic Tujia pedigree
-
S. Fu, J. Yan, X. Wang, J. Dong, P. Chen, C. Wang, and G. Chen The audiological characteristics of a hereditary Y-linked hearing loss in a Chinese ethnic Tujia pedigree Int. J. Pediatr. Otorhinolaryngol. 75 2011 202 206
-
(2011)
Int. J. Pediatr. Otorhinolaryngol.
, vol.75
, pp. 202-206
-
-
Fu, S.1
Yan, J.2
Wang, X.3
Dong, J.4
Chen, P.5
Wang, C.6
Chen, G.7
-
19
-
-
21844444077
-
Three-dimensional maps of all chromosomes in human male fibroblast nuclei and prometaphase rosettes
-
A. Bolzer, G. Kreth, I. Solovei, D. Koehler, K. Saracoglu, C. Fauth, S. Müller, R. Eils, C. Cremer, M.R. Speicher, and T. Cremer Three-dimensional maps of all chromosomes in human male fibroblast nuclei and prometaphase rosettes PLoS Biol. 3 2005 e157
-
(2005)
PLoS Biol.
, vol.3
, pp. 157
-
-
Bolzer, A.1
Kreth, G.2
Solovei, I.3
Koehler, D.4
Saracoglu, K.5
Fauth, C.6
Müller, S.7
Eils, R.8
Cremer, C.9
Speicher, M.R.10
Cremer, T.11
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