-
2
-
-
33747050669
-
Recurrent miscarriage
-
Rai R., and Regan L. Recurrent miscarriage. Lancet 368 (2006) 601-611
-
(2006)
Lancet
, vol.368
, pp. 601-611
-
-
Rai, R.1
Regan, L.2
-
3
-
-
0033358729
-
Highly skewed X-chromosome inactivation is associated with idiopathic recurrent spontaneous abortion
-
Lanasa M.C., Hogge W.A., Kubik C., Blancato J., and Hoffman E.P. Highly skewed X-chromosome inactivation is associated with idiopathic recurrent spontaneous abortion. Am J Hum Genet 65 (1999) 252-254
-
(1999)
Am J Hum Genet
, vol.65
, pp. 252-254
-
-
Lanasa, M.C.1
Hogge, W.A.2
Kubik, C.3
Blancato, J.4
Hoffman, E.P.5
-
4
-
-
33748148582
-
Extremely skewed X-chromosome inactivation patterns in women with recurrent spontaneous abortion
-
Bagislar S., Ustuner I., Cengiz B., Soylemez F., Akyerli C.B., Ceylaner S., et al. Extremely skewed X-chromosome inactivation patterns in women with recurrent spontaneous abortion. Aust N Z J Obstet Gynaecol 46 (2006) 384-387
-
(2006)
Aust N Z J Obstet Gynaecol
, vol.46
, pp. 384-387
-
-
Bagislar, S.1
Ustuner, I.2
Cengiz, B.3
Soylemez, F.4
Akyerli, C.B.5
Ceylaner, S.6
-
5
-
-
31644432219
-
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
-
(2006)
Fertil Steril
, vol.85
, pp. 441-445
-
-
Dewan, S.1
Puscheck, E.E.2
Coulam, C.B.3
Wilcox, A.J.4
Jeyendran, R.S.5
-
6
-
-
0033674607
-
The causes and consequences of random and non-random X chromosome inactivation in humans
-
Brown C.J., and Robinson W.P. The causes and consequences of random and non-random X chromosome inactivation in humans. Clin Genet 58 (2000) 353-363
-
(2000)
Clin Genet
, vol.58
, pp. 353-363
-
-
Brown, C.J.1
Robinson, W.P.2
-
7
-
-
0034828305
-
A novel X chromosome-linked genetic cause of recurrent spontaneous abortion
-
Lanasa M.C., Hogge W.A., Kubik C.J., Ness R.B., Harger J., Nagel T., et al. A novel X chromosome-linked genetic cause of recurrent spontaneous abortion. Am J Obstet Gynecol 185 (2001) 563-568
-
(2001)
Am J Obstet Gynecol
, vol.185
, pp. 563-568
-
-
Lanasa, M.C.1
Hogge, W.A.2
Kubik, C.J.3
Ness, R.B.4
Harger, J.5
Nagel, T.6
-
8
-
-
0034766550
-
Preferential X-chromosome inactivation in women with idiopathic recurrent pregnancy loss
-
Uehara S., Hashiyada M., Sato K., Sato Y., Fujimori K., and Okamura K. Preferential X-chromosome inactivation in women with idiopathic recurrent pregnancy loss. Fertil Steril 76 (2001) 908-914
-
(2001)
Fertil Steril
, vol.76
, pp. 908-914
-
-
Uehara, S.1
Hashiyada, M.2
Sato, K.3
Sato, Y.4
Fujimori, K.5
Okamura, K.6
-
9
-
-
0029051456
-
X-chromosome methylation in manifesting and healthy carriers of dystrophinopathies: concordance of activation ratios among first degree female relatives and skewed inactivation as cause of the affected phenotypes
-
Azofeifa J., Voit T., Hubner C., and Cremer M. X-chromosome methylation in manifesting and healthy carriers of dystrophinopathies: concordance of activation ratios among first degree female relatives and skewed inactivation as cause of the affected phenotypes. Hum Genet 96 (1995) 167-176
-
(1995)
Hum Genet
, vol.96
, pp. 167-176
-
-
Azofeifa, J.1
Voit, T.2
Hubner, C.3
Cremer, M.4
-
10
-
-
0030792801
-
Familial skewed X inactivation: a molecular trait associated with high spontaneous-abortion rate maps to Xq28
-
Pegoraro E., Whitaker J., Mowery-Rushton P., Surti U., Lanasa M., and Hoffman E.P. Familial skewed X inactivation: a molecular trait associated with high spontaneous-abortion rate maps to Xq28. Am J Hum Genet 61 (1997) 160-170
-
(1997)
Am J Hum Genet
, vol.61
, pp. 160-170
-
-
Pegoraro, E.1
Whitaker, J.2
Mowery-Rushton, P.3
Surti, U.4
Lanasa, M.5
Hoffman, E.P.6
-
11
-
-
0007272350
-
Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11
-
Vogt P.H., Edelmann A., Kirsch S., Henegariu O., Hirschmann P., Kiesewetter F., et al. 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
-
12
-
-
0042123550
-
Detection of sperm in men with Y chromosome microdeletions of the AZFa, AZFb and AZFc regions
-
Hopps C.V., Mielnik A., Goldstein M., Palermo G.D., Rosenwaks Z., and Schlegel P.N. Detection of sperm in men with Y chromosome microdeletions of the AZFa, AZFb and AZFc regions. Hum Reprod 18 (2003) 1660-1665
-
(2003)
Hum Reprod
, vol.18
, pp. 1660-1665
-
-
Hopps, C.V.1
Mielnik, A.2
Goldstein, M.3
Palermo, G.D.4
Rosenwaks, Z.5
Schlegel, P.N.6
-
13
-
-
33947546526
-
Molecular and clinical characterization of y chromosome microdeletions in infertile men: a 10-year experience in Italy
-
Ferlin A., Arredi B., Speltra E., Cazzadore C., Selice R., Garolla A., et al. 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
-
14
-
-
33646520137
-
The human Y chromosome: a masculine chromosome
-
Noordam M.J., and Repping S. The human Y chromosome: a masculine chromosome. Curr Opin Genet Dev 16 (2006) 225-232
-
(2006)
Curr Opin Genet Dev
, vol.16
, pp. 225-232
-
-
Noordam, M.J.1
Repping, S.2
-
15
-
-
12244292692
-
Genetic abnormalities among severely oligospermic men who are candidates for intracytoplasmic sperm injection
-
Foresta C., Garolla A., Bartoloni L., Bettella A., and Ferlin A. Genetic abnormalities among severely oligospermic men who are candidates for intracytoplasmic sperm injection. J Clin Endocrinol Metab 90 (2005) 152-156
-
(2005)
J Clin Endocrinol Metab
, vol.90
, pp. 152-156
-
-
Foresta, C.1
Garolla, A.2
Bartoloni, L.3
Bettella, A.4
Ferlin, A.5
-
16
-
-
0032911570
-
Implications of sperm chromosome abnormalities in recurrent miscarriage
-
Rubio C., Simon C., Blanco J., Vidal F., Minguez Y., Egozcue J., et al. Implications of sperm chromosome abnormalities in recurrent miscarriage. J Assist Reprod Genet 16 (1999) 253-258
-
(1999)
J Assist Reprod Genet
, vol.16
, pp. 253-258
-
-
Rubio, C.1
Simon, C.2
Blanco, J.3
Vidal, F.4
Minguez, Y.5
Egozcue, J.6
-
17
-
-
11144238934
-
Sperm chromosomal abnormalities in patients with unexplained recurrent abortions
-
Al-Hassan S., Hellani A., Al-Shahrani A., Al-Deery M., Jaroudi K., and Coskun S. Sperm chromosomal abnormalities in patients with unexplained recurrent abortions. Arch Androl 51 (2005) 69-76
-
(2005)
Arch Androl
, vol.51
, pp. 69-76
-
-
Al-Hassan, S.1
Hellani, A.2
Al-Shahrani, A.3
Al-Deery, M.4
Jaroudi, K.5
Coskun, S.6
-
18
-
-
0031458796
-
Skewed X-chromosome inactivation is common in fetuses or newborns associated with confined placental mosaicism
-
Lau A.W., Brown C.J., Penaherrera M., Langlois S., Kalousek D.K., and Robinson W.P. Skewed X-chromosome inactivation is common in fetuses or newborns associated with confined placental mosaicism. Am J Hum Genet 61 (1997) 1353-1361
-
(1997)
Am J Hum Genet
, vol.61
, pp. 1353-1361
-
-
Lau, A.W.1
Brown, C.J.2
Penaherrera, M.3
Langlois, S.4
Kalousek, D.K.5
Robinson, W.P.6
-
19
-
-
0035152359
-
Evidence of skewed X-chromosome inactivation in 47,XXY and 48,XXYY Klinefelter patients
-
Iitsuka Y., Bock A., Nguyen D.D., Samango-Sprouse C.A., Simpson J.L., and Bischoff F.Z. Evidence of skewed X-chromosome inactivation in 47,XXY and 48,XXYY Klinefelter patients. Am J Med Genet 98 (2001) 25-31
-
(2001)
Am J Med Genet
, vol.98
, pp. 25-31
-
-
Iitsuka, Y.1
Bock, A.2
Nguyen, D.D.3
Samango-Sprouse, C.A.4
Simpson, J.L.5
Bischoff, F.Z.6
-
20
-
-
0033762221
-
Age- and tissue-specific variation of X chromosome inactivation ratios in normal women
-
Sharp A., Robinson D., and Jacobs P. Age- and tissue-specific variation of X chromosome inactivation ratios in normal women. Hum Genet 107 (2000) 343-349
-
(2000)
Hum Genet
, vol.107
, pp. 343-349
-
-
Sharp, A.1
Robinson, D.2
Jacobs, P.3
-
21
-
-
33947689122
-
Recurrent spontaneous abortion and skewed X-inactivation: is there an association?
-
e1-6 [discussion 384.e6-8]
-
Hogge W.A., Prosen T.L., Lanasa M.C., Huber H.A., and Reeves M.F. Recurrent spontaneous abortion and skewed X-inactivation: is there an association?. Am J Obstet Gynecol 196 (2007) 384 e1-6 [discussion 384.e6-8]
-
(2007)
Am J Obstet Gynecol
, vol.196
, pp. 384
-
-
Hogge, W.A.1
Prosen, T.L.2
Lanasa, M.C.3
Huber, H.A.4
Reeves, M.F.5
-
22
-
-
0038209028
-
Pregnancy outcome in recurrent miscarriage patients with skewed X chromosome inactivation
-
Sullivan A.E., Lewis T., Stephenson M., Odem R., Schreiber J., Ober C., et al. Pregnancy outcome in recurrent miscarriage patients with skewed X chromosome inactivation. Obstet Gynecol 101 (2003) 1236-1242
-
(2003)
Obstet Gynecol
, vol.101
, pp. 1236-1242
-
-
Sullivan, A.E.1
Lewis, T.2
Stephenson, M.3
Odem, R.4
Schreiber, J.5
Ober, C.6
-
23
-
-
2342470545
-
X-chromosome inactivation patterns in Korean women with idiopathic recurrent spontaneous abortion
-
Kim J.W., Park S.Y., Kim Y.M., Kim J.M., Han J.Y., and Ryu H.M. X-chromosome inactivation patterns in Korean women with idiopathic recurrent spontaneous abortion. J Korean Med Sci 19 (2004) 258-262
-
(2004)
J Korean Med Sci
, vol.19
, pp. 258-262
-
-
Kim, J.W.1
Park, S.Y.2
Kim, Y.M.3
Kim, J.M.4
Han, J.Y.5
Ryu, H.M.6
-
24
-
-
0015239907
-
Possible mechanisms of X chromosome inactivation
-
Lyon M.F. Possible mechanisms of X chromosome inactivation. Nat New Biol 232 (1971) 229-232
-
(1971)
Nat New Biol
, vol.232
, pp. 229-232
-
-
Lyon, M.F.1
-
25
-
-
0029885015
-
Genetic control of X inactivation and processes leading to X-inactivation skewing
-
Belmont J.W. Genetic control of X inactivation and processes leading to X-inactivation skewing. Am J Hum Genet 58 (1996) 1101-1108
-
(1996)
Am J Hum Genet
, vol.58
, pp. 1101-1108
-
-
Belmont, J.W.1
-
26
-
-
0030928170
-
Acquired skewing of X-chromosome inactivation patterns in myeloid cells of the elderly suggests stochastic clonal loss with age
-
Gale R.E., Fielding A.K., Harrison C.N., and Linch D.C. Acquired skewing of X-chromosome inactivation patterns in myeloid cells of the elderly suggests stochastic clonal loss with age. Br J Haematol 98 (1997) 512-519
-
(1997)
Br J Haematol
, vol.98
, pp. 512-519
-
-
Gale, R.E.1
Fielding, A.K.2
Harrison, C.N.3
Linch, D.C.4
-
27
-
-
0033555008
-
Y chromosome and male infertility
-
Krausz C., and McElreavey K. Y chromosome and male infertility. Front Biosci 15 (1999) E1-E8
-
(1999)
Front Biosci
, vol.15
-
-
Krausz, C.1
McElreavey, K.2
-
28
-
-
34147168217
-
Y-chromosome haplogroups and susceptibility to azoospermia factor c microdeletion in an Italian population
-
Arredi B., Ferlin A., Speltra E., Bedin C., Zuccarello D., Ganz F., et al. Y-chromosome haplogroups and susceptibility to azoospermia factor c microdeletion in an Italian population. J Med Genet 44 (2007) 205-208
-
(2007)
J Med Genet
, vol.44
, pp. 205-208
-
-
Arredi, B.1
Ferlin, A.2
Speltra, E.3
Bedin, C.4
Zuccarello, D.5
Ganz, F.6
-
29
-
-
33751178805
-
Techniques and reasons to remain interested in the Y chromosome
-
Noordam M.J., van der Veen F., and Repping S. Techniques and reasons to remain interested in the Y chromosome. Fertil Steril 86 (2006) 1801-1802
-
(2006)
Fertil Steril
, vol.86
, pp. 1801-1802
-
-
Noordam, M.J.1
van der Veen, F.2
Repping, S.3
-
30
-
-
4043092052
-
EAA/EMQN best practice guidelines for molecular diagnosis of y-chromosomal microdeletions
-
Simoni M., Bakker E., and Krausz C. EAA/EMQN best practice guidelines for molecular diagnosis of y-chromosomal microdeletions. 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
|