-
1
-
-
0345594404
-
The undescended testis: An update
-
Mathews R., Gearhart J.P., Pohl H.G., Belman A.B., Costable R.A., Kennedy W.A., et al. The undescended testis an update . Dialogues Pediatr Urol. 20:1997;1-8.
-
(1997)
Dialogues Pediatr Urol
, vol.20
, pp. 1-8
-
-
Mathews, R.1
Gearhart, J.P.2
Pohl, H.G.3
Belman, A.B.4
Costable, R.A.5
Kennedy, W.A.6
-
2
-
-
0030952310
-
Paternity after bilateral cryptorchidism
-
Lee P.A., O'Leary L.A., Songer N.J., Coughlin M.T., Bellinger M.F., LaPorte R.E. Paternity after bilateral cryptorchidism. Arch Pediatr Adolesc Med. 151:1997;260-263.
-
(1997)
Arch Pediatr Adolesc Med
, vol.151
, pp. 260-263
-
-
Lee, P.A.1
O'Leary, L.A.2
Songer, N.J.3
Coughlin, M.T.4
Bellinger, M.F.5
Laporte, R.E.6
-
3
-
-
0029800452
-
Paternity after unilateral cryptorchidism: A controlled study
-
Lee P.A., O'Leary L.A., Songer N.J., Coughlin M.T., Bellinger M.F., LaPorte R.E. Paternity after unilateral cryptorchidism a controlled study . Pediatrics. 98:1996;676-679.
-
(1996)
Pediatrics
, vol.98
, pp. 676-679
-
-
Lee, P.A.1
O'Leary, L.A.2
Songer, N.J.3
Coughlin, M.T.4
Bellinger, M.F.5
Laporte, R.E.6
-
5
-
-
0017119580
-
Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human Y chromosome long arm
-
Tiepolo L., Zuffardi O. Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human Y chromosome long arm. Hum Genet. 34:1976;119-124.
-
(1976)
Hum Genet
, vol.34
, pp. 119-124
-
-
Tiepolo, L.1
Zuffardi, O.2
-
6
-
-
0029088061
-
Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene
-
Reijo R., Lee T., Salo P., Alagappan R., Brown L.G., Rosenberg M., et al. Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene. Nat Genet. 10:1995;383-393.
-
(1995)
Nat Genet
, vol.10
, pp. 383-393
-
-
Reijo, R.1
Lee, T.2
Salo, P.3
Alagappan, R.4
Brown, L.G.5
Rosenberg, M.6
-
7
-
-
9244243681
-
Substantial prevalence of microdeletions of the Y-chromosome in infertile men with idiopathic azoospermia and oligospermia detected using a sequence-tagged site-based strategy
-
Najmabadi H., Vivian H., Yen P., Subbarao M.N., Bhasin D., Banaag L., et al. Substantial prevalence of microdeletions of the Y-chromosome in infertile men with idiopathic azoospermia and oligospermia detected using a sequence-tagged site-based strategy. J Clin Endocrinol Metab. 81:1996;1347-1352.
-
(1996)
J Clin Endocrinol Metab
, vol.81
, pp. 1347-1352
-
-
Najmabadi, H.1
Vivian, H.2
Yen, P.3
Subbarao, M.N.4
Bhasin, D.5
Banaag, L.6
-
8
-
-
0022530702
-
A deletion map of the human Y chromosome based on DNA hybridization
-
Vergnaud G., Page D.C., Simmler M.C., Brown L., Rouyer F., Noel B., et al. A deletion map of the human Y chromosome based on DNA hybridization. Am J Hum Genet. 36:1986;109-124.
-
(1986)
Am J Hum Genet
, vol.36
, pp. 109-124
-
-
Vergnaud, G.1
Page, D.C.2
Simmler, M.C.3
Brown, L.4
Rouyer, F.5
Noel, B.6
-
9
-
-
0023921510
-
Y autosome translocations and mosaicism in the aetiology of 45,X maleness: Assignment of fertility factor to distal Yq11
-
Andersson M., Page D.C., Pettay D., Subrt I., Turleau C., de Grouchy J., et al. Y autosome translocations and mosaicism in the aetiology of 45,X maleness assignment of fertility factor to distal Yq11 . Hum Genet. 79:1988;2-7.
-
(1988)
Hum Genet
, vol.79
, pp. 2-7
-
-
Andersson, M.1
Page, D.C.2
Pettay, D.3
Subrt, I.4
Turleau, C.5
De Grouchy, J.6
-
10
-
-
0026018317
-
A deletion map of the human Yq11 region: Implications for the evolution of the Y chromosome and tentative mapping of a locus involved in spermatogenesis
-
Bardoni B., Zuffardi O., Guioli S., Ballabio A., Simi P., Cavalli P., et al. A deletion map of the human Yq11 region implications for the evolution of the Y chromosome and tentative mapping of a locus involved in spermatogenesis . Genomics. 11:1991;443-451.
-
(1991)
Genomics
, vol.11
, pp. 443-451
-
-
Bardoni, B.1
Zuffardi, O.2
Guioli, S.3
Ballabio, A.4
Simi, P.5
Cavalli, P.6
-
11
-
-
0024284028
-
A simple salting out procedure for extracting DNA from human nucleated cells
-
Miller S.A., Dykes D.D., Polesky H.F. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res. 16:1988;1215.
-
(1988)
Nucleic Acids Res
, vol.16
, pp. 1215
-
-
Miller, S.A.1
Dykes, D.D.2
Polesky, H.F.3
-
12
-
-
0029871858
-
Severe oligospermia resulting from deletions of azoospermia factor gene on Y chromosome
-
Reijo R., Alagappan R.K., Patrizio P., Page D.C. Severe oligospermia resulting from deletions of azoospermia factor gene on Y chromosome. Lancet. 347:1996;1290-1293.
-
(1996)
Lancet
, vol.347
, pp. 1290-1293
-
-
Reijo, R.1
Alagappan, R.K.2
Patrizio, P.3
Page, D.C.4
-
13
-
-
0026756965
-
The human Y chromosome: A 43-interval map based on naturally occurring deletions
-
Volrath D., Foote S., Hilton A., Brown L.G., Beer-Romero P., Bogan J.S., et al. The human Y chromosome a 43-interval map based on naturally occurring deletions . Science. 258:1992;52-59.
-
(1992)
Science
, vol.258
, pp. 52-59
-
-
Volrath, D.1
Foote, S.2
Hilton, A.3
Brown, L.G.4
Beer-Romero, P.5
Bogan, J.S.6
-
14
-
-
0031050740
-
Microdeletions in the Y chromosome of infertile men
-
Pryor J.L., Kent-First M., Muallem A., Van Bergen A.H., Nolton 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
Nolton, W.E.5
Meisner, L.6
-
15
-
-
0017174597
-
Cryptorchidism in the subfertile male
-
Lipshultz L.I. Cryptorchidism in the subfertile male. Fertil Steril. 27:1976;609-620.
-
(1976)
Fertil Steril
, vol.27
, pp. 609-620
-
-
Lipshultz, L.I.1
-
17
-
-
0024474344
-
Surgical management of undescended testis: Retrospective study of potential fertility in 274 cases
-
Okuyama A., Nonomura N., Nakamura M., Namaki M., Fujioka H., Kiyohara, et al. Surgical management of undescended testis retrospective study of potential fertility in 274 cases . J Urol. 142:1989;749-751.
-
(1989)
J Urol
, vol.142
, pp. 749-751
-
-
Okuyama, A.1
Nonomura, N.2
Nakamura, M.3
Namaki, M.4
Fujioka, H.5
Kiyohara6
-
18
-
-
0015536073
-
Fertility of patients with solitary testis
-
Woodhead D.M., Pohl D.R., Johnson D.E. Fertility of patients with solitary testis. J Urol. 100:1973;66-67.
-
(1973)
J Urol
, vol.100
, pp. 66-67
-
-
Woodhead, D.M.1
Pohl, D.R.2
Johnson, D.E.3
-
19
-
-
0027095955
-
Genetic determinants of testis development in normal and abnormal individuals
-
Hawkins J.R. Genetic determinants of testis development in normal and abnormal individuals. Intersexuality. 38:1992;62-65.
-
(1992)
Intersexuality
, vol.38
, pp. 62-65
-
-
Hawkins, J.R.1
-
20
-
-
0032323778
-
Androgen receptor gene alterations are not associated with isolated cryptorchidism
-
Wiener J.S., Marcelli M., Gonzales E.T. Jr, Roth D.R., Lamb D.J. Androgen receptor gene alterations are not associated with isolated cryptorchidism. J Urol. 160:1998;863-865.
-
(1998)
J Urol
, vol.160
, pp. 863-865
-
-
Wiener, J.S.1
Marcelli, M.2
Gonzales E.T., Jr.3
Roth, D.R.4
Lamb, D.J.5
-
21
-
-
0028926210
-
Sexually dimorphic sterility phenotypes in Hoxa10-deficient mice
-
Satokata I., Benson G., Maas R. Sexually dimorphic sterility phenotypes in Hoxa10-deficient mice. Nature. 374:1995;460-463.
-
(1995)
Nature
, vol.374
, pp. 460-463
-
-
Satokata, I.1
Benson, G.2
Maas, R.3
-
22
-
-
0029160520
-
Cryptorchidism and homeotic transformations of spinal nerves and vertabrae in Hoxa-10 deficient mice
-
Rijli F., Matyas R., Pellegrini M., Dierich A., Gruss P., Dolle P., et al. Cryptorchidism and homeotic transformations of spinal nerves and vertabrae in Hoxa-10 deficient mice. Proc Natl Acad Sci USA. 92:1995;8185-8189.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 8185-8189
-
-
Rijli, F.1
Matyas, R.2
Pellegrini, M.3
Dierich, A.4
Gruss, P.5
Dolle, P.6
-
23
-
-
0344299941
-
Analysis for alterations of the homeobox gene, HOXA10, in cryptorchid patients
-
(abstract no. 98) Nov. 1-3 New Orleans, Louisiana.
-
Kolon TF, Weiner JS, Roth DR, Gonzales ET, Lamb DJ. Analysis for alterations of the homeobox gene, HOXA10, in cryptorchid patients (abstract no. 98). In: Program and Abstracts of the 1997 Meeting of the American Academy of Pediatrics. Nov. 1-3, 1997, New Orleans, Louisiana.
-
(1997)
In: Program and Abstracts of the 1997 Meeting of the American Academy of Pediatrics
-
-
Kolon, T.F.1
Weiner, J.S.2
Roth, D.R.3
Gonzales, E.T.4
Lamb, D.J.5
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