-
1
-
-
33748675306
-
X chromosome-inactivation patterns of 1,005 phenotypically unaffected females
-
Amos-Landgraf J.M., Cottle A., Plenge R.M., Friez M., Schwartz C.E., Longshore J., and Willard H.F. X chromosome-inactivation patterns of 1,005 phenotypically unaffected females. Am. J. Hum. Genet. 79 (2006) 493-499
-
(2006)
Am. J. Hum. Genet.
, vol.79
, pp. 493-499
-
-
Amos-Landgraf, J.M.1
Cottle, A.2
Plenge, R.M.3
Friez, M.4
Schwartz, C.E.5
Longshore, J.6
Willard, H.F.7
-
2
-
-
0015717515
-
Primordial cell pool size and lineage relationships of five human cell types
-
Fialkow P.J. Primordial cell pool size and lineage relationships of five human cell types. Ann. Hum. Genet. 37 (1973) 39-48
-
(1973)
Ann. Hum. Genet.
, vol.37
, pp. 39-48
-
-
Fialkow, P.J.1
-
3
-
-
0026607007
-
Maximum-likelihood analysis of human T-cell X chromosome inactivation patterns: Normal women versus carriers of X-linked severe combined immunodeficiency
-
Puck J.M., Stewart C.C., and Nussbaum R.L. Maximum-likelihood analysis of human T-cell X chromosome inactivation patterns: Normal women versus carriers of X-linked severe combined immunodeficiency. Am. J. Hum. Genet. 50 (1992) 742-748
-
(1992)
Am. J. Hum. Genet.
, vol.50
, pp. 742-748
-
-
Puck, J.M.1
Stewart, C.C.2
Nussbaum, R.L.3
-
4
-
-
7344266327
-
Unbalanced X-chromosome inactivation in haemopoietic cells from normal women
-
Tonon L., Bergamaschi G., Dellavecchia C., Rosti V., Lucotti C., Malabarba L., Novella A., Vercesi E., Frassoni F., and Cazzola M. Unbalanced X-chromosome inactivation in haemopoietic cells from normal women. Br. J. Haematol. 102 (1998) 996-1003
-
(1998)
Br. J. Haematol.
, vol.102
, pp. 996-1003
-
-
Tonon, L.1
Bergamaschi, G.2
Dellavecchia, C.3
Rosti, V.4
Lucotti, C.5
Malabarba, L.6
Novella, A.7
Vercesi, E.8
Frassoni, F.9
Cazzola, M.10
-
5
-
-
0030723262
-
A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation
-
Plenge R.M., Hendrich B.D., Schwartz C., Arena J.F., Naumova A., Sapienza C., Winter R.M., and Willard H.F. A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation. Nat. Genet. 17 (1997) 353-356
-
(1997)
Nat. Genet.
, vol.17
, pp. 353-356
-
-
Plenge, R.M.1
Hendrich, B.D.2
Schwartz, C.3
Arena, J.F.4
Naumova, A.5
Sapienza, C.6
Winter, R.M.7
Willard, H.F.8
-
6
-
-
19244364584
-
Uneven X inactivation in a female monozygotic twin pair with Fabry disease and discordant expression of a novel mutation in the alpha-galactosidase A gene
-
Redonnet-Vernhet I., Ploos van Amstel J.K., Jansen R.P., Wevers R.A., Salvayre R., and Levade T. Uneven X inactivation in a female monozygotic twin pair with Fabry disease and discordant expression of a novel mutation in the alpha-galactosidase A gene. J. Med. Genet. 33 (1996) 682-688
-
(1996)
J. Med. Genet.
, vol.33
, pp. 682-688
-
-
Redonnet-Vernhet, I.1
Ploos van Amstel, J.K.2
Jansen, R.P.3
Wevers, R.A.4
Salvayre, R.5
Levade, T.6
-
7
-
-
1842331461
-
Haemophilia B in female twins caused by a point mutation in one factor IX gene and nonrandom inactivation patterns of the X-chromosomes
-
Schroder W., Wulff K., Wollina K., and Herrmann F.H. Haemophilia B in female twins caused by a point mutation in one factor IX gene and nonrandom inactivation patterns of the X-chromosomes. Thromb. Haemost. 78 (1997) 1347-1351
-
(1997)
Thromb. Haemost.
, vol.78
, pp. 1347-1351
-
-
Schroder, W.1
Wulff, K.2
Wollina, K.3
Herrmann, F.H.4
-
8
-
-
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
-
9
-
-
0031821968
-
Non-random X chromosome inactivation in mammalian cells
-
Migeon B.R. Non-random X chromosome inactivation in mammalian cells. Cytogenet. Cell Genet. 80 (1998) 142-148
-
(1998)
Cytogenet. Cell Genet.
, vol.80
, pp. 142-148
-
-
Migeon, B.R.1
-
10
-
-
38149097805
-
No evidence that skewing of X chromosome inactivation patterns is transmitted to offspring in humans
-
Bolduc V., Chagnon P., Provost S., Dube M.P., Belisle C., Gingras M., Mollica L., and Busque L. No evidence that skewing of X chromosome inactivation patterns is transmitted to offspring in humans. J. Clin. Invest. 118 (2008) 333-341
-
(2008)
J. Clin. Invest.
, vol.118
, pp. 333-341
-
-
Bolduc, V.1
Chagnon, P.2
Provost, S.3
Dube, M.P.4
Belisle, C.5
Gingras, M.6
Mollica, L.7
Busque, L.8
-
11
-
-
0028219438
-
Tissue specificity of X-chromosome inactivation patterns
-
Gale R.E., Wheadon H., Boulos P., and Linch D.C. Tissue specificity of X-chromosome inactivation patterns. Blood 83 (1994) 2899-2905
-
(1994)
Blood
, vol.83
, pp. 2899-2905
-
-
Gale, R.E.1
Wheadon, H.2
Boulos, P.3
Linch, D.C.4
-
12
-
-
33846708729
-
Increased skewing of X chromosome inactivation with age in both blood and buccal cells
-
Knudsen G.P., Pedersen J., Klingenberg O., Lygren I., and Orstavik K.H. Increased skewing of X chromosome inactivation with age in both blood and buccal cells. Cytogenet. Genome Res. 116 (2007) 24-28
-
(2007)
Cytogenet. Genome Res.
, vol.116
, pp. 24-28
-
-
Knudsen, G.P.1
Pedersen, J.2
Klingenberg, O.3
Lygren, I.4
Orstavik, K.H.5
-
13
-
-
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
-
14
-
-
4844226909
-
The dynamics of X-inactivation skewing as women age
-
Hatakeyama C., Anderson C.L., Beever C.L., Penaherrera M.S., Brown C.J., and Robinson W.P. The dynamics of X-inactivation skewing as women age. Clin. Genet. 66 (2004) 327-332
-
(2004)
Clin. Genet.
, vol.66
, pp. 327-332
-
-
Hatakeyama, C.1
Anderson, C.L.2
Beever, C.L.3
Penaherrera, M.S.4
Brown, C.J.5
Robinson, W.P.6
-
15
-
-
0030830125
-
A PCR-based non-radioactive X-chromosome inactivation assay for genetic counseling in X-linked primary immunodeficiencies
-
Wengler G.S., Parolini O., Fiorini M., Mella P., Smith H., Ugazio A.G., and Notarangelo L.D. A PCR-based non-radioactive X-chromosome inactivation assay for genetic counseling in X-linked primary immunodeficiencies. Life Sci. 61 (1997) 1405-1411
-
(1997)
Life Sci.
, vol.61
, pp. 1405-1411
-
-
Wengler, G.S.1
Parolini, O.2
Fiorini, M.3
Mella, P.4
Smith, H.5
Ugazio, A.G.6
Notarangelo, L.D.7
-
16
-
-
0031035442
-
Skewed X-chromosome inactivation in female carriers of dyskeratosis congenita
-
Devriendt K., Matthijs G., Legius E., Schollen E., Blockmans D., van Geet C., Degreef H., Cassiman J.J., and Fryns J.P. Skewed X-chromosome inactivation in female carriers of dyskeratosis congenita. Am. J. Hum. Genet. 60 (1997) 581-587
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 581-587
-
-
Devriendt, K.1
Matthijs, G.2
Legius, E.3
Schollen, E.4
Blockmans, D.5
van Geet, C.6
Degreef, H.7
Cassiman, J.J.8
Fryns, J.P.9
-
17
-
-
0035139995
-
Prenatal diagnosis of a familial Xq deletion in a female fetus: A case report
-
Brown L.Y., Alonso M.L., Yu J., Warburton D., and Brown S. Prenatal diagnosis of a familial Xq deletion in a female fetus: A case report. Prenat. Diagn. 21 (2001) 27-30
-
(2001)
Prenat. Diagn.
, vol.21
, pp. 27-30
-
-
Brown, L.Y.1
Alonso, M.L.2
Yu, J.3
Warburton, D.4
Brown, S.5
-
18
-
-
0026098386
-
X chromosome inactivation in fibroblasts of mentally retarded female carriers of the fragile site Xq27.3: Application of the probe M27 beta to evaluate X inactivation status
-
Schmidt M., Du Sart D., Kalitsis P., Fraser N., Leversha M., Voullaire L., Foster D., Davies J., Hills L., Petrovic V., et al. X chromosome inactivation in fibroblasts of mentally retarded female carriers of the fragile site Xq27.3: Application of the probe M27 beta to evaluate X inactivation status. Am. J. Med. Genet. 38 (1991) 411-415
-
(1991)
Am. J. Med. Genet.
, vol.38
, pp. 411-415
-
-
Schmidt, M.1
Du Sart, D.2
Kalitsis, P.3
Fraser, N.4
Leversha, M.5
Voullaire, L.6
Foster, D.7
Davies, J.8
Hills, L.9
Petrovic, V.10
-
19
-
-
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
-
20
-
-
0034478073
-
X chromosome defects as an etiology of recurrent spontaneous abortion
-
Lanasa M.C., and Hogge W.A. X chromosome defects as an etiology of recurrent spontaneous abortion. Semin. Reprod. Med. 18 (2000) 97-103
-
(2000)
Semin. Reprod. Med.
, vol.18
, pp. 97-103
-
-
Lanasa, M.C.1
Hogge, W.A.2
-
21
-
-
0033365207
-
The X chromosome and recurrent spontaneous abortion: The significance of transmanifesting carriers
-
Lanasa M.C., Hogge W.A., and Hoffman E. The X chromosome and recurrent spontaneous abortion: The significance of transmanifesting carriers. Am. J. Hum. Genet. 64 (1999) 934-938
-
(1999)
Am. J. Hum. Genet.
, vol.64
, pp. 934-938
-
-
Lanasa, M.C.1
Hogge, W.A.2
Hoffman, E.3
-
22
-
-
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
-
23
-
-
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., Prosen T., Markovic N., and Hoffman E.P. 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
Prosen, T.7
Markovic, N.8
Hoffman, E.P.9
-
24
-
-
0037318792
-
Skewed X-chromosome inactivation is associated with trisomy in women ascertained on the basis of recurrent spontaneous abortion or chromosomally abnormal pregnancies
-
Beever C.L., Stephenson M.D., Penaherrera M.S., Jiang R.H., Kalousek D.K., Hayden M., Field L., Brown C.J., and Robinson W.P. Skewed X-chromosome inactivation is associated with trisomy in women ascertained on the basis of recurrent spontaneous abortion or chromosomally abnormal pregnancies. Am. J. Hum. Genet. 72 (2003) 399-407
-
(2003)
Am. J. Hum. Genet.
, vol.72
, pp. 399-407
-
-
Beever, C.L.1
Stephenson, M.D.2
Penaherrera, M.S.3
Jiang, R.H.4
Kalousek, D.K.5
Hayden, M.6
Field, L.7
Brown, C.J.8
Robinson, W.P.9
-
25
-
-
0033365299
-
Extremely skewed X-chromosome inactivation is increased in women with recurrent spontaneous abortion
-
Sangha K.K., Stephenson M.D., Brown C.J., and Robinson W.P. Extremely skewed X-chromosome inactivation is increased in women with recurrent spontaneous abortion. Am. J. Hum. Genet. 65 (1999) 913-917
-
(1999)
Am. J. Hum. Genet.
, vol.65
, pp. 913-917
-
-
Sangha, K.K.1
Stephenson, M.D.2
Brown, C.J.3
Robinson, W.P.4
-
26
-
-
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
-
27
-
-
33947689122
-
Recurrent spontaneous abortion and skewed X-inactivation: Is there an association?
-
discussion e386-e388
-
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) e381-e386 discussion e386-e388
-
(2007)
Am J Obstet Gynecol
, vol.196
-
-
Hogge, W.A.1
Prosen, T.L.2
Lanasa, M.C.3
Huber, H.A.4
Reeves, M.F.5
-
28
-
-
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., Ceylaner G., Acar A., and Ozcelik T. 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
Ceylaner, G.7
Acar, A.8
Ozcelik, T.9
-
29
-
-
42349101246
-
Skewed X-chromosome inactivation in Greek women with idiopathic recurrent miscarriage
-
Dasoula A., Kalantaridou S., Sotiriadis A., Pavlou M., Georgiou I., Paraskevaidis E., Makrigiannakis A., and Syrrou M. Skewed X-chromosome inactivation in Greek women with idiopathic recurrent miscarriage. Fetal Diagn. Ther. 23 (2008) 198-203
-
(2008)
Fetal Diagn. Ther.
, vol.23
, pp. 198-203
-
-
Dasoula, A.1
Kalantaridou, S.2
Sotiriadis, A.3
Pavlou, M.4
Georgiou, I.5
Paraskevaidis, E.6
Makrigiannakis, A.7
Syrrou, M.8
-
30
-
-
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
-
31
-
-
43449131196
-
Association of extremely skewed X-chromosome inactivation with Taiwanese women presenting with recurrent pregnancy loss
-
Kuo P.L., Huang S.C., Chang L.W., Lin C.H., Tsai W.H., and Teng Y.N. Association of extremely skewed X-chromosome inactivation with Taiwanese women presenting with recurrent pregnancy loss. J. Formos. Med. Assoc. 107 (2008) 340-343
-
(2008)
J. Formos. Med. Assoc.
, vol.107
, pp. 340-343
-
-
Kuo, P.L.1
Huang, S.C.2
Chang, L.W.3
Lin, C.H.4
Tsai, W.H.5
Teng, Y.N.6
-
32
-
-
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., and Branch D.W. 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
Branch, D.W.7
-
33
-
-
0036182393
-
Cytogenetic analysis of miscarriages from couples with recurrent miscarriage: A case-control study
-
Stephenson M.D., Awartani K.A., and Robinson W.P. Cytogenetic analysis of miscarriages from couples with recurrent miscarriage: A case-control study. Hum. Reprod. 17 (2002) 446-451
-
(2002)
Hum. Reprod.
, vol.17
, pp. 446-451
-
-
Stephenson, M.D.1
Awartani, K.A.2
Robinson, W.P.3
-
34
-
-
0023177737
-
Chromosomal causes of fetal death
-
Warburton D. Chromosomal causes of fetal death. Clin. Obstet. Gynecol. 30 (1987) 268-277
-
(1987)
Clin. Obstet. Gynecol.
, vol.30
, pp. 268-277
-
-
Warburton, D.1
-
36
-
-
0036099646
-
Multiplex interphase FISH as a screen for common aneuploidies in spontaneous abortions
-
Jobanputra V., Sobrino A., Kinney A., Kline J., and Warburton D. Multiplex interphase FISH as a screen for common aneuploidies in spontaneous abortions. Hum. Reprod. 17 (2002) 1166-1170
-
(2002)
Hum. Reprod.
, vol.17
, pp. 1166-1170
-
-
Jobanputra, V.1
Sobrino, A.2
Kinney, A.3
Kline, J.4
Warburton, D.5
-
37
-
-
3242882723
-
Trisomic pregnancy and the oocyte pool
-
Kline J., Kinney A., Reuss M.L., Kelly A., Levin B., Ferin M., and Warburton D. Trisomic pregnancy and the oocyte pool. Hum. Reprod. 19 (2004) 1633-1643
-
(2004)
Hum. Reprod.
, vol.19
, pp. 1633-1643
-
-
Kline, J.1
Kinney, A.2
Reuss, M.L.3
Kelly, A.4
Levin, B.5
Ferin, M.6
Warburton, D.7
-
38
-
-
0033616191
-
Ovarian differentiation and gonadal failure
-
Simpson J.L., and Rajkovic A. Ovarian differentiation and gonadal failure. Am. J. Med. Genet. 89 (1999) 186-200
-
(1999)
Am. J. Med. Genet.
, vol.89
, pp. 186-200
-
-
Simpson, J.L.1
Rajkovic, A.2
-
39
-
-
0036749783
-
Genetic disorders in premature ovarian failure
-
Laml T., Preyer O., Umek W., Hengstschlager M., and Hanzal H. Genetic disorders in premature ovarian failure. Hum. Reprod. Update 8 (2002) 483-491
-
(2002)
Hum. Reprod. Update
, vol.8
, pp. 483-491
-
-
Laml, T.1
Preyer, O.2
Umek, W.3
Hengstschlager, M.4
Hanzal, H.5
-
40
-
-
34247855875
-
Skewed X-chromosome inactivation is associated with primary but not secondary ovarian failure
-
Bretherick K.L., Metzger D.L., Chanoine J.P., Panagiotopoulos C., Watson S.K., Lam W.L., Fluker M.R., Brown C.J., and Robinson W.P. Skewed X-chromosome inactivation is associated with primary but not secondary ovarian failure. Am. J. Med. Genet. A. 143A (2007) 945-951
-
(2007)
Am. J. Med. Genet. A.
, vol.143 A
, pp. 945-951
-
-
Bretherick, K.L.1
Metzger, D.L.2
Chanoine, J.P.3
Panagiotopoulos, C.4
Watson, S.K.5
Lam, W.L.6
Fluker, M.R.7
Brown, C.J.8
Robinson, W.P.9
-
41
-
-
4744344230
-
Genetic significance of skewed X-chromosome inactivation in premature ovarian failure
-
Sato K., Uehara S., Hashiyada M., Nabeshima H., Sugawara J., Terada Y., Yaegashi N., and Okamura K. Genetic significance of skewed X-chromosome inactivation in premature ovarian failure. Am. J. Med. Genet. A. 130 (2004) 240-244
-
(2004)
Am. J. Med. Genet. A.
, vol.130
, pp. 240-244
-
-
Sato, K.1
Uehara, S.2
Hashiyada, M.3
Nabeshima, H.4
Sugawara, J.5
Terada, Y.6
Yaegashi, N.7
Okamura, K.8
-
42
-
-
0026563126
-
Trisomy and age at menopause: Predicted associations given a link with rate of oocyte atresia
-
Kline J., and Levin B. Trisomy and age at menopause: Predicted associations given a link with rate of oocyte atresia. Paediatr. Perinat. Epidemiol. 6 (1992) 225-239
-
(1992)
Paediatr. Perinat. Epidemiol.
, vol.6
, pp. 225-239
-
-
Kline, J.1
Levin, B.2
-
43
-
-
26244450178
-
Biological aging and the etiology of aneuploidy
-
Warburton D. Biological aging and the etiology of aneuploidy. Cytogenet. Genome Res. 111 (2005) 266-272
-
(2005)
Cytogenet. Genome Res.
, vol.111
, pp. 266-272
-
-
Warburton, D.1
-
44
-
-
26244442676
-
The association of skewed X chromosome inactivation with aneuploidy in humans
-
Bretherick K., Gair J., and Robinson W.P. The association of skewed X chromosome inactivation with aneuploidy in humans. Cytogenet. Genome Res. 111 (2005) 260-265
-
(2005)
Cytogenet. Genome Res.
, vol.111
, pp. 260-265
-
-
Bretherick, K.1
Gair, J.2
Robinson, W.P.3
-
47
-
-
0033941292
-
Women with a reduced ovarian complement may have an increased risk for a child with Down syndrome
-
Freeman S.B., Yang Q., Allran K., Taft L.F., and Sherman S.L. Women with a reduced ovarian complement may have an increased risk for a child with Down syndrome. Am. J. Hum. Genet. 66 (2000) 1680-1683
-
(2000)
Am. J. Hum. Genet.
, vol.66
, pp. 1680-1683
-
-
Freeman, S.B.1
Yang, Q.2
Allran, K.3
Taft, L.F.4
Sherman, S.L.5
-
49
-
-
0033614662
-
Increased concentrations of follicle-stimulating hormone in mothers of children with Down's syndrome
-
van Montfrans J.M., Dorland M., Oosterhuis G.J., van Vugt J.M., Rekers-Mombarg L.T., and Lambalk C.B. Increased concentrations of follicle-stimulating hormone in mothers of children with Down's syndrome. Lancet 353 (1999) 1853-1854
-
(1999)
Lancet
, vol.353
, pp. 1853-1854
-
-
van Montfrans, J.M.1
Dorland, M.2
Oosterhuis, G.J.3
van Vugt, J.M.4
Rekers-Mombarg, L.T.5
Lambalk, C.B.6
-
50
-
-
33646490739
-
X-chromosome inactivation and ovarian age during the reproductive years
-
Kline J., Kinney A., Levin B., Kelly A., Chih-Yu J., Brown S., and Warburton D. X-chromosome inactivation and ovarian age during the reproductive years. Fertil. Steril. 85 (2006) 1488-1495
-
(2006)
Fertil. Steril.
, vol.85
, pp. 1488-1495
-
-
Kline, J.1
Kinney, A.2
Levin, B.3
Kelly, A.4
Chih-Yu, J.5
Brown, S.6
Warburton, D.7
-
51
-
-
38449087657
-
The origin of human aneuploidy: Where we have been, where we are going
-
Spec No. 2
-
Hassold T., Hall H., and Hunt P. The origin of human aneuploidy: Where we have been, where we are going. Hum Mol Genet 16 (2007) R203-R208 Spec No. 2
-
(2007)
Hum Mol Genet
, vol.16
-
-
Hassold, T.1
Hall, H.2
Hunt, P.3
-
52
-
-
0034176876
-
X-linked genetic factors regulate hematopoietic stem-cell kinetics in females
-
Christensen K., Kristiansen M., Hagen-Larsen H., Skytthe A., Bathum L., Jeune B., Andersen-Ranberg K., Vaupel J.W., and Orstavik K.H. X-linked genetic factors regulate hematopoietic stem-cell kinetics in females. Blood 95 (2000) 2449-2451
-
(2000)
Blood
, vol.95
, pp. 2449-2451
-
-
Christensen, K.1
Kristiansen, M.2
Hagen-Larsen, H.3
Skytthe, A.4
Bathum, L.5
Jeune, B.6
Andersen-Ranberg, K.7
Vaupel, J.W.8
Orstavik, K.H.9
-
53
-
-
21044450309
-
Twin study of genetic and aging effects on X chromosome inactivation
-
Kristiansen M., Knudsen G.P., Bathum L., Naumova A.K., Sorensen T.I., Brix T.H., Svendsen A.J., Christensen K., Kyvik K.O., and Orstavik K.H. Twin study of genetic and aging effects on X chromosome inactivation. Eur. J. Hum. Genet. 13 (2005) 599-606
-
(2005)
Eur. J. Hum. Genet.
, vol.13
, pp. 599-606
-
-
Kristiansen, M.1
Knudsen, G.P.2
Bathum, L.3
Naumova, A.K.4
Sorensen, T.I.5
Brix, T.H.6
Svendsen, A.J.7
Christensen, K.8
Kyvik, K.O.9
Orstavik, K.H.10
-
54
-
-
0035282880
-
Assessment of mechanism of acquired skewed X inactivation by analysis of twins
-
Vickers M.A., McLeod E., Spector T.D., and Wilson I.J. Assessment of mechanism of acquired skewed X inactivation by analysis of twins. Blood 97 (2001) 1274-1281
-
(2001)
Blood
, vol.97
, pp. 1274-1281
-
-
Vickers, M.A.1
McLeod, E.2
Spector, T.D.3
Wilson, I.J.4
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