-
1
-
-
0025708282
-
Recurrent miscarriage I
-
September, 336 (8716)
-
Stirrat GM. Recurrent miscarriage I. Definition Epidemiol Lancet : September, 1990: 15: 336 (8716): 673-675.
-
(1990)
Definition Epidemiol Lancet
, vol.15
, pp. 673-675
-
-
Stirrat, G.M.1
-
2
-
-
0030056937
-
Frequency of abnormal karyotypes among abortuses from women with and without a history of recurrent spontaneous abortion
-
Stern JJ, Darfmann AD, Gutierrez-Najar AJ, Cerrillo M, Caulam CB. Frequency of abnormal karyotypes among abortuses from women with and without a history of recurrent spontaneous abortion. Fertil Steril 1996: 65 (2): 250-253.
-
(1996)
Fertil. Steril.
, vol.65
, Issue.2
, pp. 250-253
-
-
Stern, J.J.1
Darfmann, A.D.2
Gutierrez-Najar, A.J.3
Cerrillo, M.4
Caulam, C.B.5
-
3
-
-
0027192045
-
A prospective study of 63 couples with a history of recurrent spontaneous abortion: Contributing factors and outcome of subsequent pregnancies
-
Tulppala M, Palosuo T, Ramsay T, Miettinen A, Salonen R, Ylikorkala O. A prospective study of 63 couples with a history of recurrent spontaneous abortion: contributing factors and outcome of subsequent pregnancies. Hum Reprod 1993: 8 (5): 764-770.
-
(1993)
Hum. Reprod.
, vol.8
, Issue.5
, pp. 764-770
-
-
Tulppala, M.1
Palosuo, T.2
Ramsay, T.3
Miettinen, A.4
Salonen, R.5
Ylikorkala, O.6
-
4
-
-
0027152009
-
Chromosome heteromorphisms and early recurrent abortions
-
Del Porto G, D'Alessandro E, Grommatico P, Coghi IM, DeSanctis S, Giambenedetti M et al. Chromosome heteromorphisms and early recurrent abortions. Hum Reprod 1993: 8 (5): 755-758.
-
(1993)
Hum. Reprod.
, vol.8
, Issue.5
, pp. 755-758
-
-
Del Porto, G.1
D'Alessandro, E.2
Grommatico, P.3
Coghi, I.M.4
DeSanctis, S.5
Giambenedetti, M.6
-
6
-
-
0032425535
-
Chromosome translocations segregation modes and strategies for preimplantation genetic diagnosis
-
Scriven PN, Handyside AH, Ogilvie CM. Chromosome translocations segregation modes and strategies for preimplantation genetic diagnosis. Prenat Diagn 1998: 18 (13): 1437-1449.
-
(1998)
Prenat. Diagn.
, vol.18
, Issue.13
, pp. 1437-1449
-
-
Scriven, P.N.1
Handyside, A.H.2
Ogilvie, C.M.3
-
7
-
-
0033016168
-
Clinical applications of two-color telomeric fluorescence in situ hybridization for prenatal diagnosis: Identification of chromosomal translocation in five families with recurrent miscarriages or a child with multiple congenital anomalies
-
Wakui K, Tanemyra M, Suzumori K, Hidaka E, Ishikanla M, Kubota T et al. Clinical applications of two-color telomeric fluorescence in situ hybridization for prenatal diagnosis: identification of chromosomal translocation in five families with recurrent miscarriages or a child with multiple congenital anomalies. J Hum Genet 1999: 44 (2): 85-90.
-
(1999)
J. Hum. Genet.
, vol.44
, Issue.2
, pp. 85-90
-
-
Wakui, K.1
Tanemyra, M.2
Suzumori, K.3
Hidaka, E.4
Ishikanla, M.5
Kubota, T.6
-
8
-
-
0033851883
-
An optimized set of human telomere clones for studying telomere integrity and architecture
-
Knight SJL, Lese CM, Precht HS, Kuc J, Ning Y, Lucas S et al. An optimized set of human telomere clones for studying telomere integrity and architecture. Am J Hum Genet 2000: 67: 320-332.
-
(2000)
Am. J. Hum. Genet.
, vol.67
, pp. 320-332
-
-
Knight, S.J.L.1
Lese, C.M.2
Precht, H.S.3
Kuc, J.4
Ning, Y.5
Lucas, S.6
-
9
-
-
0034046292
-
Perfect endings a review of subtelomeric probes and their use in clinical diagnosis
-
Knight SJ, Flint J. Perfect endings a review of subtelomeric probes and their use in clinical diagnosis. J Med Genet 2000: 37 (6): 401-409.
-
(2000)
J. Med. Genet.
, vol.37
, Issue.6
, pp. 401-409
-
-
Knight, S.J.1
Flint, J.2
-
10
-
-
0033764929
-
The promise and pitfalls of telomere region-spesific probes
-
Ballif BC , Kashorie CD, Shaffer LG. The promise and pitfalls of telomere region-spesific probes. Am J Hum Genet 2000: 67: 1356-1359.
-
(2000)
Am. J. Hum. Genet.
, vol.67
, pp. 1356-1359
-
-
Ballif, B.C.1
Kashorie, C.D.2
Shaffer, L.G.3
-
11
-
-
0034608441
-
Detection of a cryptic translocation in a family with mental retardation using FISH and telomere region-specific probes
-
Bacino CA, Kashork CD, Davino NA, Shaffer LG. Detection of a cryptic translocation in a family with mental retardation using FISH and telomere region-specific probes. Am J Med Genet 2000: 92: 250-255.
-
(2000)
Am. J. Med. Genet.
, vol.92
, pp. 250-255
-
-
Bacino, C.A.1
Kashork, C.D.2
Davino, N.A.3
Shaffer, L.G.4
-
12
-
-
0033909534
-
Familial mental retardation syndrome ATR × 16 due to an inherited cryptic subtelomeric translocation, t (3; 16) (q29; p13.3)
-
Holinski-Feder E, Reyniers E, Uhrig S, Golla A, Wauters J, Kroisel P et al. Familial mental retardation syndrome ATR × 16 due to an inherited cryptic subtelomeric translocation, t (3; 16) (q29; p13.3). Am J Hum Genet., 66: 16-25., 2000.
-
(2000)
Am. J. Hum. Genet.
, vol.66
, pp. 16-25
-
-
Holinski-Feder, E.1
Reyniers, E.2
Uhrig, S.3
Golla, A.4
Wauters, J.5
Kroisel, P.6
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