-
1
-
-
79952209117
-
Chromosome territories, X; Y translocation and premature ovarian failure: Is there a relationship?
-
Lissoni S, Baronchelli S, Villa N, Lucchini V, Betri E, Cavalli P, et al. Chromosome territories, X; Y translocation and premature ovarian failure: is there a relationship? Mol Cytogenet. 2009; 2:19.
-
(2009)
Mol Cytogenet
, vol.2
, pp. 19
-
-
Lissoni, S.1
Baronchelli, S.2
Villa, N.3
Lucchini, V.4
Betri, E.5
Cavalli, P.6
-
2
-
-
77957201712
-
A prospective evaluation of antral follicle function in women with 46, XX spontaneous primary ovarian insufficiency
-
Hubayter ZR, Popat V, Vanderhoof VH, Ndubizu O, Johnson D, Mao E, et al. A prospective evaluation of antral follicle function in women with 46, XX spontaneous primary ovarian insufficiency. Fertil Steril. 2010; 94(5): 1769-1774.
-
(2010)
Fertil Steril
, vol.94
, Issue.5
, pp. 1769-1774
-
-
Hubayter, Z.R.1
Popat, V.2
Vanderhoof, V.H.3
Ndubizu, O.4
Johnson, D.5
Mao, E.6
-
3
-
-
77952542159
-
Mutational analysis of inhibin alpha gene revealed three novel variations in Indian women with premature ovarian failure
-
Prakash, GJ, Ravi Kanth, VV, Shelling AN, Rozati, R, Sujatha, M. Mutational analysis of inhibin alpha gene revealed three novel variations in Indian women with premature ovarian failure. Fertil Steril. 2010; 94(1): 90-98.
-
(2010)
Fertil Steril
, vol.94
, Issue.1
, pp. 90-98
-
-
Prakash, G.J.1
Ravi Kanth, V.V.2
Shelling, A.N.3
Rozati, R.4
Sujatha, M.5
-
4
-
-
80054736935
-
Pathogenesis and causes of premature ovarian failure: An update
-
Ebrahimi M, Akbari Asbagh F. Pathogenesis and causes of premature ovarian failure: an update. Int J Fertil Steril. 2011; 5(2): 54-65.
-
(2011)
Int J Fertil Steril
, vol.5
, Issue.2
, pp. 54-65
-
-
Ebrahimi, M.1
Akbari Asbagh, F.2
-
6
-
-
0035235040
-
The X chromosome and the ovary
-
Zinn AR. The X chromosome and the ovary. J Soc Gynecol Investig. 2001; 8 Suppl Proceedings 1: S34-36.
-
(2001)
J Soc Gynecol Investig
, vol.8
, Issue.SUPPL. 1
-
-
Zinn, A.R.1
-
7
-
-
33749576976
-
Molecular cytogenetic studies of Xq critical region in premature ovarian failure patients
-
Portnoï MF, Aboura A, Tachdjian G, Bouchard P, Dewailly D, Bourcigaux N, et al. Molecular cytogenetic studies of Xq critical region in premature ovarian failure patients. Hum Reprod. 2006; 21(9): 2329-2334.
-
(2006)
Hum Reprod
, vol.21
, Issue.9
, pp. 2329-2334
-
-
Portnoï, M.F.1
Aboura, A.2
Tachdjian, G.3
Bouchard, P.4
Dewailly, D.5
Bourcigaux, N.6
-
8
-
-
0035878326
-
X/autosomal translocations in the Xq critical region associated with premature ovarian failure fall within and outside genes
-
Mumm S, Herrera L, Waeltz PW, Scardovi A, Nagaraja R, Esposito T, et al. X/autosomal translocations in the Xq critical region associated with premature ovarian failure fall within and outside genes. Genomics. 2001; 76(1-3): 30-36.
-
(2001)
Genomics
, vol.76
, Issue.1-3
, pp. 30-36
-
-
Mumm, S.1
Herrera, L.2
Waeltz, P.W.3
Scardovi, A.4
Nagaraja, R.5
Esposito, T.6
-
9
-
-
33646496697
-
Chromosomal rearrangements in Xq and premature ovarian failure: Mapping of 25 new cases and review of the literature
-
Rizzolio F, Bione S, Sala C, Goegan M, Gentile M, Gregato G, et al. Chromosomal rearrangements in Xq and premature ovarian failure: mapping of 25 new cases and review of the literature. Hum Reprod. 2006; 21(6): 1477-1483.
-
(2006)
Hum Reprod
, vol.21
, Issue.6
, pp. 1477-1483
-
-
Rizzolio, F.1
Bione, S.2
Sala, C.3
Goegan, M.4
Gentile, M.5
Gregato, G.6
-
10
-
-
0027440971
-
Deletion (X) (q26.1->q28) in a proband and her mother: Molecular characterization and phenotypic- karyotypic deductions
-
Tharapel AT, Anderson KP, Simpson JL, Martens PR, Wilroy RS Jr, Llerena JC Jr, et al. Deletion (X) (q26.1->q28) in a proband and her mother: molecular characterization and phenotypic- karyotypic deductions. Am J Hum Genet. 1993; 52(3): 463-471.
-
(1993)
Am J Hum Genet
, vol.52
, Issue.3
, pp. 463-471
-
-
Tharapel, A.T.1
Anderson, K.P.2
Simpson, J.L.3
Martens, P.R.4
Wilroy Jr., R.S.5
Llerena Jr., J.C.6
-
11
-
-
0028087750
-
Molecular and cytogenetic studies of an X; autosome translocation in a patient with premature ovarian failure and review of the literature
-
Powell CM, Taggart RT, Drumheller TC, Wangsa D, Qian C, Nelson LM, et al. Molecular and cytogenetic studies of an X; autosome translocation in a patient with premature ovarian failure and review of the literature. Am J Med Genet. 1994; 52(1): 19-26.
-
(1994)
Am J Med Genet
, vol.52
, Issue.1
, pp. 19-26
-
-
Powell, C.M.1
Taggart, R.T.2
Drumheller, T.C.3
Wangsa, D.4
Qian, C.5
Nelson, L.M.6
-
12
-
-
77954685093
-
X-chromosome terminal deletion in a female with premature ovarian failure: Haplo insufficiency of X-linked genes as a possible explanation
-
Ferreira SI, Matoso E, Pinto M, Almeida J, Liehr T, Melo JB, et al. X-chromosome terminal deletion in a female with premature ovarian failure: Haplo insufficiency of X-linked genes as a possible explanation. Mol Cytogenet. 2010; 3: 14.
-
(2010)
Mol Cytogenet
, vol.3
, pp. 14
-
-
Ferreira, S.I.1
Matoso, E.2
Pinto, M.3
Almeida, J.4
Liehr, T.5
Melo, J.B.6
-
13
-
-
0034065580
-
Mapping of the POF1 locus and identification of putative genes for premature ovarian failure
-
Davison RM, Fox M, Conway GS. Mapping of the POF1 locus and identification of putative genes for premature ovarian failure. Mol Hum Reprod. 2000; 6(4): 314-318.
-
(2000)
Mol Hum Reprod
, vol.6
, Issue.4
, pp. 314-318
-
-
Davison, R.M.1
Fox, M.2
Conway, G.S.3
-
15
-
-
0016804341
-
Human X-autosome translocations: Differential inactivation of the X chromosome in a kindred with an X-9 translocation
-
Leisti JT, Kaback MM, Rimoin DL. Human X-autosome translocations: differential inactivation of the X chromosome in a kindred with an X-9 translocation. Am J Hum Genet. 1975; 27(4): 441-453.
-
(1975)
Am J Hum Genet
, vol.27
, Issue.4
, pp. 441-453
-
-
Leisti, J.T.1
Kaback, M.M.2
Rimoin, D.L.3
-
16
-
-
0020604023
-
9 translocation, primary amenorrhea, and hypothalamic dysfunction
-
Gardner HA, McConnon JK, MacKenzie MA, An X 9 translocation, primary amenorrhea, and hypothalamic dysfunction. Am J Med Genet. 1983;14(4):647-656.
-
(1983)
Am J Med Genet
, vol.14
, Issue.4
, pp. 647-656
-
-
Gardner, H.A.1
McConnon, J.K.2
Mackenzie, M.A.3
An, X.4
-
17
-
-
0035016354
-
Phenotypic effects of balanced X-autosome translocations in females: A retrospective survey of 104 cases reported from UK laboratories
-
Waters JJ, Campbell PL, Crocker AJ, Campbell CM. Phenotypic effects of balanced X-autosome translocations in females: a retrospective survey of 104 cases reported from UK laboratories. Hum Genet. 2001; 108(4): 318-327.
-
(2001)
Hum Genet
, vol.108
, Issue.4
, pp. 318-327
-
-
Waters, J.J.1
Campbell, P.L.2
Crocker, A.J.3
Campbell, C.M.4
-
18
-
-
21244434753
-
Premature ovarian failure
-
Goswami D, Conway GS. Premature ovarian failure. Hum Reprod Update. 2005; 11(4): 391-410.
-
(2005)
Hum Reprod Update
, vol.11
, Issue.4
, pp. 391-410
-
-
Goswami, D.1
Conway, G.S.2
-
19
-
-
77957732285
-
A teenager with a t(X; 17) (q22; q25) and ovarian failure
-
Martínez-Valenzuela M, Rivera H, Mundo-Ayala JN, González-Mercado MG, Davalos-Rodríguez IP. A teenager with a t(X; 17) (q22; q25) and ovarian failure. Genet Couns. 2010; 21(3): 269-275.
-
(2010)
Genet Couns
, vol.21
, Issue.3
, pp. 269-275
-
-
Martínez-Valenzuela, M.1
Rivera, H.2
Mundo-Ayala, J.N.3
González-Mercado, M.G.4
Davalos-Rodríguez, I.P.5
-
20
-
-
77951759840
-
Premature ovarian failure, absence of pubic and axillary hair with de novo 46, X, t(X;15) (q24;q26.3)
-
Giacomozzi C, Gullotta F, Federico G, Colapietro I, Nardone AM, Cianfarani S. Premature ovarian failure, absence of pubic and axillary hair with de novo 46, X, t(X;15) (q24;q26.3). Am J Med Genet A. 2010;152A (5):1305-1309.
-
(2010)
Am J Med Genet A
, vol.152
, Issue.5
, pp. 1305-1309
-
-
Giacomozzi, C.1
Gullotta, F.2
Federico, G.3
Colapietro, I.4
Nardone, A.M.5
Cianfarani, S.6
-
21
-
-
33745929656
-
Microarray detection of a de novo der (X) t (X; 11) (q28; p13) in a girl with premature ovarian failure and features of BeckwithWiedemann syndrome
-
Han JY, Shin JH, Han MS, Je GH, Shaffer LG. Microarray detection of a de novo der (X) t (X; 11) (q28; p13) in a girl with premature ovarian failure and features of BeckwithWiedemann syndrome. J Hum Genet. 2006; 51(7):641-643.
-
(2006)
J Hum Genet
, vol.51
, Issue.7
, pp. 641-643
-
-
Han, J.Y.1
Shin, J.H.2
Han, M.S.3
Je, G.H.4
Shaffer, L.G.5
-
22
-
-
84881181201
-
Genetic causes of premature ovarian failure (POF) and early menopause
-
Simpson JL. Genetic causes of premature ovarian failure (POF) and early menopause. Int J Fertil Steril. 2011;5 Suppl. 1:I41.
-
(2011)
Int J Fertil Steril
, vol.5
, Issue.SUPPL. 1
-
-
Simpson, J.L.1
-
23
-
-
0019521313
-
Balanced reciprocal (X;9) translocation in a girl with primary amenorrhea
-
Leddet-Chevallier I, Reid RA, Carrel RE, Sparkes RS. Balanced reciprocal (X;9) translocation in a girl with primary amenorrhea. Ann Genet. 1981; 24(3): 162-164.
-
(1981)
Ann Genet
, vol.24
, Issue.3
, pp. 162-164
-
-
Leddet-Chevallier, I.1
Reid, R.A.2
Carrel, R.E.3
Sparkes, R.S.4
|