-
1
-
-
0031005450
-
A Turner-like phenotype in a girl with an isodicentric fluorescent Y chromosome mosaicism
-
Bergendi E, Plochl E, Vlasak I, Rittinger O, Muss W. 1997. A Turner-like phenotype in a girl with an isodicentric fluorescent Y chromosome mosaicism. Klin Padiatr 209: 133-136.
-
(1997)
Klin Padiatr
, vol.209
, pp. 133-136
-
-
Bergendi, E.1
Plochl, E.2
Vlasak, I.3
Rittinger, O.4
Muss, W.5
-
2
-
-
0028817026
-
Comparative genomic hybridization in clinical cytogenetics
-
Bryndorf T, Kirchchoftt M, Rose H, et al. 1995. Comparative genomic hybridization in clinical cytogenetics. Am J Hum Genet 57: 1211-1220.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 1211-1220
-
-
Bryndorf, T.1
Kirchchoftt, M.2
Rose, H.3
-
3
-
-
0032868065
-
Structural unbalanced chromosome rearrangements resolved by comparative genomic hybridization
-
Daniely M, Barkai G, Godman B, Avidam-Goldring A. 1999. Structural unbalanced chromosome rearrangements resolved by comparative genomic hybridization. Cytogenet Cell Genet 86: 51-55.
-
(1999)
Cytogenet Cell Genet
, vol.86
, pp. 51-55
-
-
Daniely, M.1
Barkai, G.2
Godman, B.3
Avidam-Goldring, A.4
-
4
-
-
0035106642
-
Short stature as the only presenting feature in a patient with isodicentric (Y)(q11.23) and gonadoblastoma: A clinical and molecular cytogenetic study
-
Giltay JC, Ausems MG, van Seumeren I, et al. 2001. Short stature as the only presenting feature in a patient with isodicentric (Y)(q11.23) and gonadoblastoma: a clinical and molecular cytogenetic study. Eur J Pediatr 160: 154-158.
-
(2001)
Eur J Pediatr
, vol.160
, pp. 154-158
-
-
Giltay, J.C.1
Ausems, M.G.2
Van Seumeren, I.3
-
5
-
-
0024508414
-
Prenatal diagnosis of 45,X/46,XY mosaicism-a review and update
-
Hsu LYF. 1989. Prenatal diagnosis of 45, X/46,XY mosaicism-a review and update. Prenat Diagn 9: 31-48.
-
(1989)
Prenat Diagn
, vol.9
, pp. 31-48
-
-
Hsu, L.Y.F.1
-
6
-
-
0031785299
-
Presence of the AZF region in a female with an idic(Y)(q11)
-
Jenderny J, Schmidt W, Held KR. 1998. Presence of the AZF region in a female with an idic(Y)(q11). Clin Genet 54: 341-344.
-
(1998)
Clin Genet
, vol.54
, pp. 341-344
-
-
Jenderny, J.1
Schmidt, W.2
Held, K.R.3
-
7
-
-
0033861780
-
FISH deletion mapping defines a single location for the Y chromosome stature gene, CGY
-
Kirsch S, Weiss B, De Rosa M, Ogata T, Lombardi G, Rappold GA. 2000. FISH deletion mapping defines a single location for the Y chromosome stature gene, CGY. J Med Genet 37: 593-599.
-
(2000)
J Med Genet
, vol.37
, pp. 593-599
-
-
Kirsch, S.1
Weiss, B.2
De Rosa, M.3
Ogata, T.4
Lombardi, G.5
Rappold, G.A.6
-
8
-
-
0035107689
-
Prognostic value of Y deletion analysis. The prognostic role of the extent of Y microdeletion on spermatogenesis and maturity of Sertoli cells
-
Kleiman SE, Maymon BBS, Yogev L, Paz G, Yavetz H. 2001. Prognostic value of Y deletion analysis. The prognostic role of the extent of Y microdeletion on spermatogenesis and maturity of Sertoli cells. Hum Reprod 16: 399-409.
-
(2001)
Hum Reprod
, vol.16
, pp. 399-409
-
-
Kleiman, S.E.1
Maymon, B.B.S.2
Yogev, L.3
Paz, G.4
Yavetz, H.5
-
10
-
-
0034038610
-
The role of Y chromosome deletions in male infertility
-
Ma K, Mallidis C, Bhasin S. 2000. The role of Y chromosome deletions in male infertility. Eur J Endocrinol 142: 418-430.
-
(2000)
Eur J Endocrinol
, vol.142
, pp. 418-430
-
-
Ma, K.1
Mallidis, C.2
Bhasin, S.3
-
11
-
-
0033822374
-
Screening for AZF deletion in a large series of severely impaired spermatogenesis patients
-
Martínez MC, Bernabé MJ, Gomez E, et al. 2000. Screening for AZF deletion in a large series of severely impaired spermatogenesis patients. J Androl 21: 651-655.
-
(2000)
J Androl
, vol.21
, pp. 651-655
-
-
Martínez, M.C.1
Bernabé, M.J.2
Gomez, E.3
-
12
-
-
0035105786
-
Identification of two de novo partial trisomies by comparative genomic hybridization
-
Rigola MA, Carrera M, Ribas I, et al. 2001. Identification of two de novo partial trisomies by comparative genomic hybridization. Clin Genet 59: 106-110.
-
(2001)
Clin Genet
, vol.59
, pp. 106-110
-
-
Rigola, M.A.1
Carrera, M.2
Ribas, I.3
-
13
-
-
0032934043
-
A molecular and FISH analysis of structurally abnormal Y-chromosomes in patients with Turner syndrome
-
Robinson DO, Dalton P, Jacobs PA, et al. 1999. A molecular and FISH analysis of structurally abnormal Y-chromosomes in patients with Turner syndrome. J Med Genet 36: 279-284.
-
(1999)
J Med Genet
, vol.36
, pp. 279-284
-
-
Robinson, D.O.1
Dalton, P.2
Jacobs, P.A.3
-
14
-
-
0029912473
-
Karyotyping human chromosomes by combinatorial multi-fluor-FISH
-
Speicher MR, Ballard SG, Ward DC. 1996. Karyotyping human chromosomes by combinatorial multi-fluor-FISH. Nature Genet 12: 368-375.
-
(1996)
Nature Genet
, vol.12
, pp. 368-375
-
-
Speicher, M.R.1
Ballard, S.G.2
Ward, D.C.3
-
15
-
-
0033066915
-
Molecular cytogenetic techniques for the diagnosis of chromosomal abnormalities in childhood disease
-
Stumm M, Tönnies H, Wieacker PF. 1999. Molecular cytogenetic techniques for the diagnosis of chromosomal abnormalities in childhood disease. Eur J Pediatr 158: 531-536.
-
(1999)
Eur J Pediatr
, vol.158
, pp. 531-536
-
-
Stumm, M.1
Tönnies, H.2
Wieacker, P.F.3
-
16
-
-
0029858102
-
Molecular studies in three patients with isodicentric Y chromosome
-
Stuppia L, Calabarese G, Franchi PG, et al. 1996. Molecular studies in three patients with isodicentric Y chromosome. Hum Genet 98: 691-695.
-
(1996)
Hum Genet
, vol.98
, pp. 691-695
-
-
Stuppia, L.1
Calabarese, G.2
Franchi, P.G.3
-
17
-
-
0032781538
-
45,X/46,XY Mosaicism: Report of 27 Cases
-
Telvi L, Lebbar A, Del Pino O, Barber JP, Chaussain JL. 1999. 45,X/46,XY Mosaicism: report of 27 Cases. Pediatrics 104: 304-308.
-
(1999)
Pediatrics
, vol.104
, pp. 304-308
-
-
Telvi, L.1
Lebbar, A.2
Del Pino, O.3
Barber, J.P.4
Chaussain, J.L.5
-
18
-
-
0028866305
-
Prenatal identification of i(Yp) by molecular cytogenetic analysis
-
Wang BBT, Yu LCh, Peng W, Falk RE, Williams J. 1995. Prenatal identification of i(Yp) by molecular cytogenetic analysis. Prenat Diagn 15: 1115-1119.
-
(1995)
Prenat Diagn
, vol.15
, pp. 1115-1119
-
-
Wang, B.B.T.1
Yu, L.Ch.2
Peng, W.3
Falk, R.E.4
Williams, J.5
-
19
-
-
0027161490
-
Characterization of the i(18p) in prenatal diagnosis by fluorescence in situ hybridization
-
Yu LC, Williams J Wang BT, et al. 1993. Characterization of the i(18p) in prenatal diagnosis by fluorescence in situ hybridization. Prenat Diagn 13: 355-361.
-
(1993)
Prenat Diagn
, vol.13
, pp. 355-361
-
-
Yu, L.C.1
Williams, J.2
Wang, B.T.3
|