-
1
-
-
0019442758
-
Rates of chromosome abnormalities at different maternal ages
-
Hook E.B. Rates of chromosome abnormalities at different maternal ages. Obstet Gynecol. 58:1981;282-285
-
(1981)
Obstet Gynecol
, vol.58
, pp. 282-285
-
-
Hook, E.B.1
-
2
-
-
0002589119
-
Chromosomal abnormalities in spontaneous abortion: Frequency, pathology and genetic, counseling
-
Oxford: Blackwell Scientific;
-
Simpson JL, Bombard A, Bennett MJ, Edmonds DK, eds. Chromosomal abnormalities in spontaneous abortion: frequency, pathology and genetic, counseling. In: Spontaneous and recurrent abortion. Oxford: Blackwell Scientific; 1987:51-76
-
(1987)
Spontaneous and Recurrent Abortion
, pp. 51-76
-
-
Simpson, J.L.1
Bombard, A.2
Bennett, M.J.3
Edmonds, D.K.4
-
3
-
-
0004235880
-
-
ACOG Committee Opinion Number 189, October 1997. Committee on Genetics. American College of Obstetricians and Gynecologists
-
ACOG Committee Opinion. Advanced paternal age: risks to the fetus. Number 189, October. Committee on Genetics. American College of Obstetricians and Gynecologists
-
(1997)
Advanced Paternal Age: Risks to the Fetus
-
-
-
9
-
-
0001912649
-
Familial ovarian failure
-
New York, NY: Springer-Verlag;
-
Layman LC, Lobo RA, ed. Familial ovarian failure. In: Perimenopause. New York, NY: Springer-Verlag; 1997:46-77
-
(1997)
Perimenopause
, pp. 46-77
-
-
Layman, L.C.1
Lobo, R.A.2
-
10
-
-
0032723189
-
Screening for 21-hydroxylase-deficient nonclassic adrenal hyperplasia among hyperandrogenic women: A prospective study
-
Azziz R., Hincapie L.A., Knochenhauer E.S., Dewailly D., Fox L., Boots L.R. Screening for 21-hydroxylase-deficient nonclassic adrenal hyperplasia among hyperandrogenic women a prospective study. Fertil Steril. 72:1999;915-925
-
(1999)
Fertil Steril
, vol.72
, pp. 915-925
-
-
Azziz, R.1
Hincapie, L.A.2
Knochenhauer, E.S.3
Dewailly, D.4
Fox, L.5
Boots, L.R.6
-
11
-
-
0029025333
-
Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens
-
Chillon M., 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. 332:1995;1475-1480
-
(1995)
N Engl J Med
, vol.332
, pp. 1475-1480
-
-
Chillon, M.1
Casals, T.2
Mercier, B.3
Bassas, L.4
Lissens, W.5
Silber, S.6
-
12
-
-
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 J.M., Delomel-Vinner E., Decaestecker B., Lafitte J.J., et al. Congenital bilateral absence of the vas deferens (CBAVD) and cystic fibrosis transmembrane regulator (CFTR) correlation between genotype and phenotype. Hum Genet. 97:1996;7-10
-
(1996)
Hum Genet
, vol.97
, pp. 7-10
-
-
Dumur, V.1
Gervais, R.2
Rigot, J.M.3
Delomel-Vinner, E.4
Decaestecker, B.5
Lafitte, J.J.6
-
13
-
-
0025922098
-
Cytogenetic studies in male infertility: A review
-
De Braekeleer M., Dao T.N. Cytogenetic studies in male infertility a review. Hum Reprod. 6:1991;245-250
-
(1991)
Hum Reprod
, vol.6
, pp. 245-250
-
-
De Braekeleer, M.1
Dao, T.N.2
-
14
-
-
0031050740
-
Microdeletions in the Y chromosome of infertile men
-
Pryor J.L., Kent-First M., Muallem A., Van Bergen A.H., Nolten W.E., Meisner L., et al. Microdeletions in the Y chromosome of infertile men. N Engl J Med. 336:1997;534-539
-
(1997)
N Engl J Med
, vol.336
, pp. 534-539
-
-
Pryor, J.L.1
Kent-First, M.2
Muallem, A.3
Van Bergen, A.H.4
Nolten, W.E.5
Meisner, L.6
-
15
-
-
0030323575
-
The incidence and possible relevance of Y-linked microdeletions in babies born after intracytoplasmic sperm injection and their infertile fathers
-
Kent-First M.G., 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 intracytoplasmic sperm injection and their infertile fathers. Mol Hum Reprod. 2:1996;943-950
-
(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
-
16
-
-
0031728392
-
AZFb deletions predict the absence of spermatozoa with testicular sperm extraction: Preliminary report of a prognostic genetic test
-
Brandell R.A., Mielnik A., Liotta D., Ye Z., Veeck L.L., Palermo G.D., et al. AZFb deletions predict the absence of spermatozoa with testicular sperm extraction preliminary report of a prognostic genetic test. Hum Reprod. 13:1998;2812-2815
-
(1998)
Hum Reprod
, vol.13
, pp. 2812-2815
-
-
Brandell, R.A.1
Mielnik, A.2
Liotta, D.3
Ye, Z.4
Veeck, L.L.5
Palermo, G.D.6
-
17
-
-
0033803789
-
Prognostic value of Y deletion analysis: What is the clinical prognostic value of Y chromosome microdeletion analysis?
-
Krausz C., Quintana-Murei L., McElreavey K. Prognostic value of Y deletion analysis what is the clinical prognostic value of Y chromosome microdeletion analysis? Hum Reprod. 15:2000;1431-1434
-
(2000)
Hum Reprod
, vol.15
, pp. 1431-1434
-
-
Krausz, C.1
Quintana-Murei, L.2
McElreavey, K.3
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