-
1
-
-
15644362992
-
Sex chromosome abnormalities found among 34910 new-born children: Results of a 13 years incidence study in Arhus
-
Nielsen J, Wohlert M. Sex chromosome abnormalities found among 34910 new-born children: results of a 13 years incidence study in Arhus. Birth Defects 1990;26:289-96
-
(1990)
Birth Defects
, vol.26
, pp. 289-296
-
-
Nielsen, J.1
Wohlert, M.2
-
2
-
-
0029021639
-
Turner syndrome and female sex chromosome aberrations: Deduction of the principal factors involved in the development of clinical features
-
Ogata T, Matsuo N. Turner syndrome and female sex chromosome aberrations: deduction of the principal factors involved in the development of clinical features. Hum Genet 1995;95:607-29
-
(1995)
Hum Genet
, vol.95
, pp. 607-629
-
-
Ogata, T.1
Matsuo, N.2
-
3
-
-
0026507034
-
Le syndrome de Turner: Une revolution
-
Rochiccioli P, Tauber MT. Le syndrome de Turner: une revolution. Arch Fr Pediatr 1992;49: 153-5
-
(1992)
Arch Fr Pediatr
, vol.49
, pp. 153-155
-
-
Rochiccioli, P.1
Tauber, M.T.2
-
4
-
-
0013663724
-
Chromosome preparations of leucocytes cultured from human peripheral blood
-
Moorhead PS, Nowell PC, Hellmann WJ, et al. Chromosome preparations of leucocytes cultured from human peripheral blood. Exp Cell Res 1960; 20:613
-
(1960)
Exp Cell Res
, vol.20
, pp. 613
-
-
Moorhead, P.S.1
Nowell, P.C.2
Hellmann, W.J.3
-
5
-
-
0025276497
-
Turner's syndrome. Review of the literature with reference to a successful pregnancy outcome
-
Kaneko N, Kawagoe S, Hiroi M. Turner's syndrome. Review of the literature with reference to a successful pregnancy outcome. Gynecol Obstet Invest 1990;29:81-7
-
(1990)
Gynecol Obstet Invest
, vol.29
, pp. 81-87
-
-
Kaneko, N.1
Kawagoe, S.2
Hiroi, M.3
-
8
-
-
0027238129
-
Syndrome de Turner et grossesse. A propos d'un cas
-
Guerquin B. Syndrome de Turner et grossesse. A propos d'un cas. Rev Fr Gynecol Obstet 1993;88: 342-4
-
(1993)
Rev Fr Gynecol Obstet
, vol.88
, pp. 342-344
-
-
Guerquin, B.1
-
9
-
-
0026439128
-
Deletion of the short arm of the X chromosome: A hereditary form of Turner syndrome
-
Massa G, Vanderschueren-Lodeweyckx M, Fryns JP. Deletion of the short arm of the X chromosome: a hereditary form of Turner syndrome. Eur J Pediatr 1992;151:893-94
-
(1992)
Eur J Pediatr
, vol.151
, pp. 893-894
-
-
Massa, G.1
Vanderschueren-Lodeweyckx, M.2
Fryns, J.P.3
-
10
-
-
0028203512
-
A woman with an apparent non-mosaic 45,X delivered a 46,X,der(X) liveborn female
-
Palka G, Calabrese G, Stuppia L, et al. A woman with an apparent non-mosaic 45,X delivered a 46,X,der(X) liveborn female. Clin Genet 1994;45: 93-6
-
(1994)
Clin Genet
, vol.45
, pp. 93-96
-
-
Palka, G.1
Calabrese, G.2
Stuppia, L.3
-
11
-
-
0026335903
-
Ullrich-Turner syndrome in mother and daughter: Prenatal diagnosis of a 46,X,del(X)(p21) offspring from a 45,X mother with low-level mosaicism for the del(X)(p21) in one ovary
-
Varela M, Shapira E, Hyman DB. Ullrich-Turner syndrome in mother and daughter: prenatal diagnosis of a 46,X,del(X)(p21) offspring from a 45,X mother with low-level mosaicism for the del(X)(p21) in one ovary. Am J Med Genet 1991;39: 411-12
-
(1991)
Am J Med Genet
, vol.39
, pp. 411-412
-
-
Varela, M.1
Shapira, E.2
Hyman, D.B.3
-
13
-
-
0019420493
-
Pregnancy in the Turner syndrome with only 45,X constitution
-
Wray HL, Freeman MUR, Ming PML. Pregnancy in the Turner syndrome with only 45,X constitution. Fertil Steril 1981;35:509-14
-
(1981)
Fertil Steril
, vol.35
, pp. 509-514
-
-
Wray, H.L.1
Freeman, M.U.R.2
Ming, P.M.L.3
-
14
-
-
0022505262
-
Oocyte development in X0 foetuses of man and mouse: The possible role of heterologous X-chromosome pairing in germ cell survival
-
Speed RM. Oocyte development in X0 foetuses of man and mouse: the possible role of heterologous X-chromosome pairing in germ cell survival. Chromosoma 1986;94:115-24
-
(1986)
Chromosoma
, vol.94
, pp. 115-124
-
-
Speed, R.M.1
-
16
-
-
0024308008
-
Chromosome studies and fertility treatment in women with ovarian failure
-
Hens L, Devroey P, Van Waesberghe L, et al. Chromosome studies and fertility treatment in women with ovarian failure. Clin Genet 1989; 36:81-91
-
(1989)
Clin Genet
, vol.36
, pp. 81-91
-
-
Hens, L.1
Devroey, P.2
Van Waesberghe, L.3
|