-
1
-
-
0018407084
-
The chromosomal basis for human infertility
-
Chandley AC. The chromosomal basis for human infertility. Br Med Bull 1979; 35: 181-6.
-
(1979)
Br Med Bull
, vol.35
, pp. 181-186
-
-
Chandley, A.C.1
-
2
-
-
0030317394
-
Prospective follow-up study of 877 children born after intracytoplasmatic sperm injection (ICSI), with ejaculated epididymal and testicular spermatozoa and after replacement of cryopreserved embryos obtained after ICSI
-
Bonduelle M, Wilikens A, Buysse A, van Assche E, Wisanto A, Devroey P et al. Prospective follow-up study of 877 children born after intracytoplasmatic sperm injection (ICSI), with ejaculated epididymal and testicular spermatozoa and after replacement of cryopreserved embryos obtained after ICSI. Hum Reprod 1996; 11 suppl 4; 131-59.
-
(1996)
Hum Reprod
, vol.11
, Issue.4 SUPPL.
, pp. 131-159
-
-
Bonduelle, M.1
Wilikens, A.2
Buysse, A.3
Van Assche, E.4
Wisanto, A.5
Devroey, P.6
-
3
-
-
1842411314
-
Chromosomal findings in 150 couples referred for genetic counselling prior to intracytoplasmatic sperm injection
-
Mau UA, Backert IT, Kaiser P, Kiesel L. Chromosomal findings in 150 couples referred for genetic counselling prior to intracytoplasmatic sperm injection. Hum Reprod 1997; 12: 930-7.
-
(1997)
Hum Reprod
, vol.12
, pp. 930-937
-
-
Mau, U.A.1
Backert, I.T.2
Kaiser, P.3
Kiesel, L.4
-
4
-
-
0032110611
-
Current status of the molecular diagnosis of Y-chromosomal microdeletipns in the work-up of male infertility
-
Simoni M, Kamischke A, Nieschlag E. Current status of the molecular diagnosis of Y-chromosomal microdeletipns in the work-up of male infertility. Hum Reprod 1998; 13: 1764-8.
-
(1998)
Hum Reprod
, vol.13
, pp. 1764-1768
-
-
Simoni, M.1
Kamischke, A.2
Nieschlag, E.3
-
5
-
-
0030317035
-
Cytogenetics of infertile male
-
van Assche E, Bonduelle M, Tournaye H, Joris H, Verheyen G, Devroey P et al. Cytogenetics of infertile male. Hum Reprod 1996; 11 suppl 4; 1-24.
-
(1996)
Hum Reprod
, vol.11
, Issue.4 SUPPL.
, pp. 1-24
-
-
Van Assche, E.1
Bonduelle, M.2
Tournaye, H.3
Joris, H.4
Verheyen, G.5
Devroey, P.6
-
6
-
-
0029118115
-
Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure
-
Aittomäki K, Dieguez Lucena JL, Pakarinen P, Sistonen P, Tapanainen JS, Gromoll J et al. Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure. Cell 1995; 82: 959-68.
-
(1995)
Cell
, vol.82
, pp. 959-968
-
-
Aittomäki, K.1
Dieguez Lucena, J.L.2
Pakarinen, P.3
Sistonen, P.4
Tapanainen, J.S.5
Gromoll, J.6
-
7
-
-
1842376911
-
Men homozygous for an inactivating mutation of the follicle-stimulating hormone (FSH) receptor gene present variable suppression of spermatogenesis and fertility
-
Tapanainen JS, Aittomäki K, Min J, Vaskivou T, Huhtaniemi IT. Men homozygous for an inactivating mutation of the follicle-stimulating hormone (FSH) receptor gene present variable suppression of spermatogenesis and fertility. Nat Genet 1997; 15: 205-6.
-
(1997)
Nat Genet
, vol.15
, pp. 205-206
-
-
Tapanainen, J.S.1
Aittomäki, K.2
Min, J.3
Vaskivou, T.4
Huhtaniemi, I.T.5
-
8
-
-
0029819642
-
The genetic and clinical heterogeneity of gonadotropin-releasing hormone deficiency in the human
-
Waldstreicher J, Seminara SB, Jameson JL, Greyer A, Nachtigall LB, Boepple PA et al. The genetic and clinical heterogeneity of gonadotropin-releasing hormone deficiency in the human. J Clin Endocrinol Metab 1996; 81: 4388-95.
-
(1996)
J Clin Endocrinol Metab
, vol.81
, pp. 4388-4395
-
-
Waldstreicher, J.1
Seminara, S.B.2
Jameson, J.L.3
Greyer, A.4
Nachtigall, L.B.5
Boepple, P.A.6
-
9
-
-
0025800526
-
Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy
-
La Spada AR, Wilson EM, Lubahn DB, Harding AE, Fischbeck KH. Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy. Nature 1991; 352: 77-9.
-
(1991)
Nature
, vol.352
, pp. 77-79
-
-
La Spada, A.R.1
Wilson, E.M.2
Lubahn, D.B.3
Harding, A.E.4
Fischbeck, K.H.5
-
10
-
-
0030694396
-
Long polyglutamine tracts in the androgen receptor are associated with reduced trans-activation, impaired sperm production, and male infertility
-
Tut TG, Ghadessy FJ, Trifiro MA, Pinsky L, Yong EL. Long polyglutamine tracts in the androgen receptor are associated with reduced trans-activation, impaired sperm production, and male infertility. J Clin Endocrinol Metab 1997; 82; 3777-82.
-
(1997)
J Clin Endocrinol Metab
, vol.82
, pp. 3777-3782
-
-
Tut, T.G.1
Ghadessy, F.J.2
Trifiro, M.A.3
Pinsky, L.4
Yong, E.L.5
-
11
-
-
0029025333
-
Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens
-
Chillon MC, Casals T, Mercier B, Bassas L, Lissens W, Silber S et al. Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens. N Engl J Med 1995; 332: 1475-80.
-
(1995)
N Engl J Med
, vol.332
, pp. 1475-1480
-
-
Chillon, M.C.1
Casals, T.2
Mercier, B.3
Bassas, L.4
Lissens, W.5
Silber, S.6
-
12
-
-
0030765634
-
Congenital absence of the vas deferens: Incomplete penetrance of the cystic fibrosis gene mutations
-
Shin D, Gilbert F, Goldstein M, Sclegel PN. Congenital absence of the vas deferens: incomplete penetrance of the cystic fibrosis gene mutations. J Urol 1997; 158: 1794-8.
-
(1997)
J Urol
, vol.158
, pp. 1794-1798
-
-
Shin, D.1
Gilbert, F.2
Goldstein, M.3
Sclegel, P.N.4
-
13
-
-
0031666951
-
Female patients with cystic fibrosis suffer from reproductive endocrinological disorders despite good clinical status
-
Johannesson M, Landgren BM, Csemiczky G, Hjelte L, Gottlieb C. Female patients with cystic fibrosis suffer from reproductive endocrinological disorders despite good clinical status. Hum Reprod 1998; 13: 2092-7.
-
(1998)
Hum Reprod
, vol.13
, pp. 2092-2097
-
-
Johannesson, M.1
Landgren, B.M.2
Csemiczky, G.3
Hjelte, L.4
Gottlieb, C.5
-
14
-
-
0030032379
-
Congenital bilateral absence of the vas deferens (CBAVD) and cystic fibrosis transmembrane regulator (CFTR): Correlation between genotype and phenotype
-
Dumur V, Gervais R, Rigot JM, Delomer-Vinner E, Decaestecker B, Lafitte JJ et al. Congenital bilateral absence of the vas deferens (CBAVD) and cystic fibrosis transmembrane regulator (CFTR): correlation between genotype and phenotype. Hum Genet 1996; 97: 7-10.
-
(1996)
Hum Genet
, vol.97
, pp. 7-10
-
-
Dumur, V.1
Gervais, R.2
Rigot, J.M.3
Delomer-Vinner, E.4
Decaestecker, B.5
Lafitte, J.J.6
-
15
-
-
24344496987
-
Förlossningar och barn födda efter provrörsbefruktingar 1982-1995
-
Socialstyrelsen: Förlossningar och barn födda efter provrörsbefruktingar 1982-1995. SoS-Rapport 1998:7.
-
(1998)
SoS-Rapport
, pp. 7
-
-
Socialstyrelsen1
-
16
-
-
0031872238
-
A birth in non-mosaic Klinefelter's syndrome after testicular fine needle aspiration, intracytoplasmic sperm injection and preimplantation genetic diagnosis
-
Reubinoff BE, Abeliovich D, Werner M, Schenker JG, Safran A, Lewin A et al. A birth in non-mosaic Klinefelter's syndrome after testicular fine needle aspiration, intracytoplasmic sperm injection and preimplantation genetic diagnosis. Hum Reprod 1998; 13: 1887-92.
-
(1998)
Hum Reprod
, vol.13
, pp. 1887-1892
-
-
Reubinoff, B.E.1
Abeliovich, D.2
Werner, M.3
Schenker, J.G.4
Safran, A.5
Lewin, A.6
-
17
-
-
0031826410
-
Multiple deletions of mitochondrial DNA are associated with the decline of motility and fertility of human spermatozoa
-
Kao SH, Chao HT, Wei YH. Multiple deletions of mitochondrial DNA are associated with the decline of motility and fertility of human spermatozoa. Mol Hum Reprod 1998; 4: 657-66.
-
(1998)
Mol Hum Reprod
, vol.4
, pp. 657-666
-
-
Kao, S.H.1
Chao, H.T.2
Wei, Y.H.3
-
18
-
-
0030323575
-
The incidence and possible relevance of Y-linked microdeletions in babies born after intracytoplasmatic sperm injection and their infertile fathers
-
Kent-First MG, Kol S, Muallem A, Ofir R, Manor D, Blazer S et al. The incidence and possible relevance of Y-linked microdeletions in babies born after intracytoplasmatic sperm injection and their infertile fathers. Mol Hum Reprod 1996; 2: 943-50.
-
(1996)
Mol Hum Reprod
, vol.2
, pp. 943-950
-
-
Kent-First, M.G.1
Kol, S.2
Muallem, A.3
Ofir, R.4
Manor, D.5
Blazer, S.6
-
19
-
-
0029936059
-
Micromanipulative assisted fertilization - Still clinical research
-
Bui TH, Wramsby H. Micromanipulative assisted fertilization - still clinical research. Hum Reprod 1996; 11: 925-6.
-
(1996)
Hum Reprod
, vol.11
, pp. 925-926
-
-
Bui, T.H.1
Wramsby, H.2
-
20
-
-
0031716239
-
Are the new microfertilization techniques associated with an increased genetic risk to the offspring?
-
Lundin K, Hanson C, Hamberger L. Are the new microfertilization techniques associated with an increased genetic risk to the offspring? Acta Obstet Gynecol Scand 1998; 77: 792-8.
-
(1998)
Acta Obstet Gynecol Scand
, vol.77
, pp. 792-798
-
-
Lundin, K.1
Hanson, C.2
Hamberger, L.3
|