-
1
-
-
0022640035
-
Incidence of premature ovarian failure
-
C.B. Coulam, S.C. Adamson, J.F. Annegers, Incidence of premature ovarian failure, Obstet. Gynecol. 67 (4) (1986) 604-606.
-
(1986)
Obstet. Gynecol
, vol.67
, Issue.4
, pp. 604-606
-
-
Coulam, C.B.1
Adamson, S.C.2
Annegers, J.F.3
-
2
-
-
0030065174
-
Characteriza-tion of idiopathic premature ovarian failure
-
G.S. Conway, G. Kaltsas, A. Patel, M.C. Davies, H.S. Jacobs, Characteriza-tion of idiopathic premature ovarian failure, Fertil. Steril. 65 (2) (1996) 337-341.
-
(1996)
Fertil. Steril
, vol.65
, Issue.2
, pp. 337-341
-
-
Conway, G.S.1
Kaltsas, G.2
Patel, A.3
Davies, M.C.4
Jacobs, H.S.5
-
3
-
-
39149108084
-
Recent advances in the study of genes involved in non-syndromic premature ovarian failure
-
P. Laissue, G. Vinci, R. A. Veitia, M. Fellous, Recent advances in the study of genes involved in non-syndromic premature ovarian failure, Mol. Cell Endocrinol. 282 (1-2) (2008) 101-111.
-
(2008)
Mol. Cell Endocrinol
, vol.282
, Issue.1-2
, pp. 101-111
-
-
Laissue, P.1
Vinci, G.2
Veitia, R.A.3
Fellous, M.4
-
5
-
-
84863573475
-
Cytogenetic analysis of 531 Chinese women with premature ovarian failure
-
X. Jiao, C. Qin, J. Li, Y. Qin, X. Gao, B. Zhang, et al., Cytogenetic analysis of 531 Chinese women with premature ovarian failure, Hum. Reprod. 27 (7) (2012) 2201-2207.
-
(2012)
Hum. Reprod
, vol.27
, Issue.7
, pp. 2201-2207
-
-
Jiao, X.1
Qin, C.2
Li, J.3
Qin, Y.4
Gao, X.5
Zhang, B.6
-
6
-
-
0032566960
-
Genes and premature ovarian failure
-
S. Christin-Maitre, C. Vasseu r, M.-F. Portnoi, P. Bouchard, Genes and premature ovarian failure, Mol. Cell. Endocrinol. 145 (1-2) (1998) 75-80.
-
(1998)
Mol. Cell. Endocrinol
, vol.145
, Issue.1-2
, pp. 75-80
-
-
Christin-Maitre, S.1
Vasseu, R.C.2
Portnoi, M.-F.3
Bouchard, P.4
-
7
-
-
84877596393
-
Cytogenetic analysis of 179 Iranian women with pre-mature ovarian failure
-
H. Kalantari, T. Madani, S. Zari Moradi, Z. Mansouri, N. Almadani, H. Gourabi, et al., Cytogenetic analysis of 179 Iranian women with pre-mature ovarian failure, Gynecol. Endocrinol. 29 (6) (2013) 588-591.
-
(2013)
Gynecol. Endocrinol
, vol.29
, Issue.6
, pp. 588-591
-
-
Kalantari, H.1
Madani, T.2
Zari Moradi, S.3
Mansouri, Z.4
Almadani, N.5
Gourabi, H.6
-
8
-
-
77955418561
-
Genetic abnormalities in Turkish women with premature ovarian failure
-
G. Ceylaner, S.O. Altinkaya, L. Mollamahmut oglu, S. Ceylaner, Genetic abnormalities in Turkish women with premature ovarian failure, Int. J. Gynaecol. Obstet. 110 (2) (2010) 122-124.
-
(2010)
Int. J. Gynaecol. Obstet
, vol.110
, Issue.2
, pp. 122-124
-
-
Ceylaner, G.1
Altinkaya, S.O.2
Mollamahmut Oglu, L.3
Ceylaner, S.4
-
9
-
-
79952216712
-
Cytogenetic analyses of premature ovarian failure using karyo-typing and interphase fluorescence in situ hybridization (FISH) in a group of 1000 patients
-
B. Lakhal,R. Braham,R. Berguigua,N. Bouali M. Zaouali,M. Chaieb, et al., Cytogenetic analyses of premature ovarian failure using karyo-typing and interphase fluorescence in situ hybridization (FISH) in a group of 1000 patients, Clin. Genet. 78 (2 2010 181-185.
-
(2010)
Clin. Genet
, vol.78
, Issue.2
, pp. 181-185
-
-
Lakhal, B.1
Braham, R.2
Berguigua, R.3
Bouali, N.4
Zaouali, M.5
Chaieb, M.6
-
10
-
-
0037101861
-
Genes and translocations involved in POF
-
D. Schlessinger, L. Herrera, L. Crisponi, S. Mumm, A. Percesepe, M. Pellegrini, et al., Genes and translocations involved in POF, Am. J. Med. Genet. 111 (3) (2002) 328-333.
-
(2002)
Am. J. Med. Genet
, vol.111
, Issue.3
, pp. 328-333
-
-
Schlessinger, D.1
Herrera, L.2
Crisponi, L.3
Mumm, S.4
Percesepe, A.5
Pellegrini, M.6
-
11
-
-
33749576976
-
Molecular cytogenetic studies of Xq critical regions in premature ovarian failure patients
-
M.-F. Portnoi, A. Aboura, G. Tachdjian, P. Bouchard, D. Dewailly, N. Bourcigaux, et al., Molecular cytogenetic studies of Xq critical regions in premature ovarian failure patients, Hum. Reprod. 21 ( 9) (2006) 2329-2334.
-
(2006)
Hum. Reprod
, vol.21
, Issue.9
, pp. 2329-2334
-
-
Portnoi, M.-F.1
Aboura, A.2
Tachdjian, G.3
Bouchard, P.4
Dewailly, D.5
Bourcigaux, N.6
-
12
-
-
17644423933
-
Premature ovarian failure associated with a small terminal Xq deletion: Narrowing the POF1 region down to Xq27.2/Xq27.3-qter
-
T. Eggermann, D. Meschede, H. Schuler, S. Palm, D. Glaser, B. Horsthemke, et al., Premature ovarian failure associated with a small terminal Xq deletion: narrowing the POF1 region down to Xq27.2/Xq27.3-qter, Clin. Genet. 67 (5) (2005) 434-437.
-
(2005)
Clin. Genet
, vol.67
, Issue.5
, pp. 434-437
-
-
Eggermann, T.1
Meschede, D.2
Schuler, H.3
Palm, S.4
Glaser, D.5
Horsthemke, B.6
-
13
-
-
6444220656
-
A susceptibility gene for p remature ovarian failure (POF) maps to proxi-mal Xq28
-
F. Rossetti, F. Rizzolio, T. Pramparo, C. Sala, S. Bione, F. Bernardi, et al., A susceptibility gene for p remature ovarian failure (POF) maps to proxi-mal Xq28, Eur. J. Hum. Genet. 12 (10) (2004) 829-834.
-
(2004)
Eur. J. Hum. Genet
, vol.12
, Issue.10
, pp. 829-834
-
-
Rossetti, F.1
Rizzolio, F.2
Pramparo, T.3
Sala, C.4
Bione, S.5
Bernardi, F.6
-
14
-
-
0033762922
-
Molecular definition of Xq common-deleted region in patients affected by premature ovarian failure
-
A. Marozzi, E. Manfredini, M.G. Tibiletti, D. Furlan, N. Villa, W. Vegetti, et al., Molecular definition of Xq common-deleted region in patients affected by premature ovarian failure, Hum. Genet. 107 (4) (2000) 304-311.
-
(2000)
Hum. Genet
, vol.107
, Issue.4
, pp. 304-311
-
-
Marozzi, A.1
Manfredini, E.2
Tibiletti, M.G.3
Furlan, D.4
Villa, N.5
Vegetti, W.6
-
15
-
-
77953506817
-
A case of premature ovarian failure (POF) in a 31-year-old woman with a 47XXX karyotype
-
P. Skalba, A. Cygal, Z. Gierzynska, A case of premature ovarian failure (POF) in a 31-year-old woman with a 47,XXX karyotype, Endokrynol. Pol. 61 (2) (2010) 217-219.
-
(2010)
Endokrynol. Pol
, vol.61
, Issue.2
, pp. 217-219
-
-
Skalba, P.1
Cygal, A.2
Gierzynska, Z.3
-
16
-
-
0141889040
-
Prevalence of the triple X syndrome in phenotypically normal women with premature ovarian failure and its association with autoimmune thyroid disorders
-
R. Goswami, D. Goswami, M. Kabra, N. Gupta, S. Dubey, V. Dadhwal, Prevalence of the triple X syndrome in phenotypically normal women with premature ovarian failure and its association with autoimmune thyroid disorders, Fertil. Steril. 80 (4) (2003) 1052-1054.
-
(2003)
Fertil. Steril
, vol.80
, Issue.4
, pp. 1052-1054
-
-
Goswami, R.1
Goswami, D.2
Kabra, M.3
Gupta, N.4
Dubey, S.5
Dadhwal, V.6
-
17
-
-
3242679937
-
An N-terminal WT1 mutation (P181S) in an XY patient with ambiguous genitalia, normal testosterone production, absence of kidney disease and associated heart defect: Enlarging the phenotypic spectrum of WT1 defects
-
B. Kohler, C. Pienkowski, F. Audran, M. Delsol, M. Tauber, F. Paris, et al., An N-terminal WT1 mutation (P181S) in an XY patient with ambiguous genitalia, normal testosterone production, absence of kidney disease and associated heart defect: enlarging the phenotypic spectrum of WT1 defects, Eur. J. Endocrinol. 150 (6) (2004) 825-830.
-
(2004)
Eur J. Endocrinol
, vol.150
, Issue.6
, pp. 825-830
-
-
Kohler, B.1
Pienkowski, C.2
Audran, F.3
Delsol, M.4
Tauber, M.5
Paris, F.6
-
18
-
-
0036277895
-
Gonadal determ ination and adrenal development are regulated by the orphan nuclear receptor steroidogenic factor-1, in a dose-dependent manner
-
J.C. Achermann, G. Ozisik, M. Ito, U.A. Orun, K. Harmanci, B. Gura-kan, et al., Gonadal determ ination and adrenal development are regulated by the orphan nuclear receptor steroidogenic factor-1, in a dose-dependent manner, J. Clin. Endocrinol. Metab. 87 (4) (2002) 1829-1833.
-
(2002)
J. Clin. Endocrinol. Metab
, vol.87
, Issue.4
, pp. 1829-1833
-
-
Achermann, J.C.1
Ozisik, G.2
Ito, M.3
Orun, U.A.4
Harmanci, K.5
Gurakan, B.6
-
19
-
-
0041852775
-
The molecular action and regulation of the testis-determining factors, SRY (sex-determining region on the y chromosome) and SOX9 [SRY-related high-mobility group ( HMG) box 9
-
V.R. Harley, M.J. Clarkson, A. Argentaro, The molecular action and regulation of the testis-determining factors, SRY (sex-determining region on the Y chromosome) and SOX9 [SRY-related high-mobility group ( HMG) box 9], Endocr. Rev. 24 (4) (2003) 466-487.
-
(2003)
Endocr. Rev
, vol.24
, Issue.4
, pp. 466-487
-
-
Harley, V.R.1
Clarkson, M.J.2
Argentaro, A.3
-
20
-
-
0031657526
-
Discordant phenotypes and 45,X/46,X,idic(Y
-
T.E. Kelly, J.B. Franko, A. Rogol, W.L. Golden, Discordant phenotypes and 45,X/46,X,idic(Y), J. Med. Genet. 35 (10) (1998) 862-864.
-
(1998)
J Med. Genet
, vol.35
, Issue.10
, pp. 862-864
-
-
Kelly, T.E.1
Franko, J.B.2
Rogol, A.3
Golden, W.L.4
-
21
-
-
79952235003
-
Cytogenetics of premature ovarian failure: An investiga-tion on 269 affected women
-
S. Baronchelli, D. Conconi, E. Panzeri, A. Bentivegna, S. Redaelli, S. Lissoni, et al., Cytogenetics of premature ovarian failure: an investiga-tion on 269 affected women, J. Biomed. Biotechnol. 2011 (2011) 370195.
-
(2011)
J. Biomed. Biotechnol
, vol.2011
, pp. 370195
-
-
Baronchelli, S.1
Conconi, D.2
Panzeri, E.3
Bentivegna, A.4
Redaelli, S.5
Lissoni, S.6
-
22
-
-
77954836426
-
Human studies on genetics of the age at natural menopause: A systematic review
-
M. Voorhuis, N.C. Onland-Moret, Y.T. van der Schouw, B.C. Fauser, F.J. Broekmans, Human studies on genetics of the age at natural menopause: a systematic review, H um. Reprod. Update 16 (4) (2010) 364-377.
-
(2010)
Hum. Reprod. Update
, vol.16
, Issue.4
, pp. 364-377
-
-
Voorhuis, M.1
Onland-Moret, N.C.2
Van Der Schouw, Y.T.3
Fauser, B.C.4
Broekmans, F.J.5
-
23
-
-
66649089490
-
Loci at chromosomes 13, 19 and 20 influence age at n atural menopause
-
L. Stolk, G. Zhai, J.B. van Meurs, M.M. Verbiest, J.A. Visser, K. Estrada, et al., Loci at chromosomes 13, 19 and 20 influence age at n atural menopause, Nat. Genet. 41 (6) (2009) 645-647.
-
(2009)
Nat. Genet
, vol.41
, Issue.6
, pp. 645-647
-
-
Stolk, L.1
Zhai, G.2
Van Meurs, J.B.3
Verbiest, M.M.4
Visser, J.A.5
Estrada, K.6
-
24
-
-
66649090056
-
Genome-wide association studies identify loci associated with a ge at menarche and age at natural menopause
-
C. He, P. Kraft, C. Chen, J.E. Buring, G. Pare, S.E. Hankinson, et al., Genome-wide association studies identify loci associated with a ge at menarche and age at natural menopause, Nat. Genet. 41 (6) (2009) 724-728.
-
(2009)
Nat. Genet
, vol.41
, Issue.6
, pp. 724-728
-
-
He, C.1
Kraft, P.2
Chen, C.3
Buring, J.E.4
Pare, G.5
Hankinson, S.E.6
|