-
1
-
-
0024313591
-
Confirmation of a balanced chromosomal translocation using molecular techniques
-
Smart RD, Retief AE, Overhauser J. Confirmation of a balanced chromosomal translocation using molecular techniques. Prenat Diagn 1989;9:505-13.
-
(1989)
Prenat Diagn
, vol.9
, pp. 505-513
-
-
Smart, R.D.1
Retief, A.E.2
Overhauser, J.3
-
2
-
-
0024835025
-
Diagnostic de remaniements chromosomiques de petite taille par la cytogénétique moleculaire
-
Taviaux S, Moncla A, Girauld F, Demaille J, Mattei JF, Mattei MG. Diagnostic de remaniements chromosomiques de petite taille par la cytogénétique moleculaire. Ann Genet (Paris) 1989;32:204-10.
-
(1989)
Ann Genet (Paris)
, vol.32
, pp. 204-210
-
-
Taviaux, S.1
Moncla, A.2
Girauld, F.3
Demaille, J.4
Mattei, J.F.5
Mattei, M.G.6
-
3
-
-
0025653203
-
Reassessment of two apparent deletions of chromosome 16p to an ins(11;16) and a t(1;16) by chromosome painting
-
Callen DF, Baker E, Eyre HJ, Chernos JE, Bell JA, Sutherland GR. Reassessment of two apparent deletions of chromosome 16p to an ins(11;16) and a t(1;16) by chromosome painting. Ann Genet (Paris) 1990;33:219-21.
-
(1990)
Ann Genet (Paris)
, vol.33
, pp. 219-221
-
-
Callen, D.F.1
Baker, E.2
Eyre, H.J.3
Chernos, J.E.4
Bell, J.A.5
Sutherland, G.R.6
-
4
-
-
0026505059
-
Detection of subtle reciprocal translocation by fluorescence in situ hybridization
-
Speleman F, Van Roy N, Wiegant J, et al. Detection of subtle reciprocal translocation by fluorescence in situ hybridization. Clin Genet 1992;41:169-174.
-
(1992)
Clin Genet
, vol.41
, pp. 169-174
-
-
Speleman, F.1
Van Roy, N.2
Wiegant, J.3
-
5
-
-
0027324051
-
Clarification of subtle reciprocal rearrangements using fluorescence in situ hybridization
-
Sullivan SA, Leana-Cox J, Schwartz S. Clarification of subtle reciprocal rearrangements using fluorescence in situ hybridization. Am J Med Genet 1993;47:223-30.
-
(1993)
Am J Med Genet
, vol.47
, pp. 223-230
-
-
Sullivan, S.A.1
Leana-Cox, J.2
Schwartz, S.3
-
6
-
-
0028926835
-
Fetal translocation between chromosomes 2,18 and 21 resolved by FISH
-
Delaroche I, Sabani M, Calabrese G, Mingarelli R, Palka G, Dallapiccola B. Fetal translocation between chromosomes 2,18 and 21 resolved by FISH. Prenat Diagn 1995;15:278-81.
-
(1995)
Prenat Diagn
, vol.15
, pp. 278-281
-
-
Delaroche, I.1
Sabani, M.2
Calabrese, G.3
Mingarelli, R.4
Palka, G.5
Dallapiccola, B.6
-
7
-
-
0027440149
-
Application of fluorescent in situ hybridization for "de novo" anomalies in prenatal diagnosis
-
Van Opstal D, Eussen HJ, Van Hemel JO, Sachs ES. Application of fluorescent in situ hybridization for "de novo" anomalies in prenatal diagnosis. Prenat Diagn 1993;13:825-32.
-
(1993)
Prenat Diagn
, vol.13
, pp. 825-832
-
-
Van Opstal, D.1
Eussen, H.J.2
Van Hemel, J.O.3
Sachs, E.S.4
-
8
-
-
0027762161
-
11q trisomy detected by fluorescence in situ hybridization
-
Takano T, Yamonouchi Y, Kawashima S, et al. 11q trisomy detected by fluorescence in situ hybridization. Clin Genet 1993;44:324-8.
-
(1993)
Clin Genet
, vol.44
, pp. 324-328
-
-
Takano, T.1
Yamonouchi, Y.2
Kawashima, S.3
-
9
-
-
0028256107
-
Prenatal diagnosis of partial trisomy 1q using fluorescent in situ hybridization
-
DuPont BR, Huff RW, Ridgway LE, Stratton RF, Moore CM. Prenatal diagnosis of partial trisomy 1q using fluorescent in situ hybridization. Am J Med Genet 1994;50:21-7.
-
(1994)
Am J Med Genet
, vol.50
, pp. 21-27
-
-
DuPont, B.R.1
Huff, R.W.2
Ridgway, L.E.3
Stratton, R.F.4
Moore, C.M.5
-
10
-
-
0025815704
-
Trisomy 12 in chronic lymphocytic leukemia: An interphase cytogenetic study
-
Pérez-Losada A, Wessman M, Tiainen M, et al. Trisomy 12 in chronic lymphocytic leukemia: an interphase cytogenetic study. Blood 1991;78:775-9.
-
(1991)
Blood
, vol.78
, pp. 775-779
-
-
Pérez-Losada, A.1
Wessman, M.2
Tiainen, M.3
-
11
-
-
0028276217
-
On the scoring of FISH-"painted" chromosome-type exchange aberrations
-
Savage JRK, Simpson P. On the scoring of FISH-"painted" chromosome-type exchange aberrations. Mutat Res 1994; 307:345-53.
-
(1994)
Mutat Res
, vol.307
, pp. 345-353
-
-
Savage, J.R.K.1
Simpson, P.2
-
12
-
-
0028924015
-
A proposed system for scoring structural aberrations detected by chromosome painting
-
Tucker JD, Morgan WF, Awa AA, et al. A proposed system for scoring structural aberrations detected by chromosome painting. Cytogenet Cell Genet 1995;68:211-21.
-
(1995)
Cytogenet Cell Genet
, vol.68
, pp. 211-221
-
-
Tucker, J.D.1
Morgan, W.F.2
Awa, A.A.3
-
13
-
-
0026528277
-
De novo complex chromosome rearrangement in identical twins with multiple congenital anomalies
-
Wakita Y, Narahara K, Tsujï K, et al. De novo complex chromosome rearrangement in identical twins with multiple congenital anomalies. Hum Genet 1992;88:596-8.
-
(1992)
Hum Genet
, vol.88
, pp. 596-598
-
-
Wakita, Y.1
Narahara, K.2
Tsujï, K.3
-
14
-
-
0027234561
-
Application of molecular and cytogenetic techniques to the detection of a de novo unbalanced t(11q;21q) in a patient previously diagnosed as having monosomy 21
-
Hertz B, Brandt CA, Petersen MB, et al. Application of molecular and cytogenetic techniques to the detection of a de novo unbalanced t(11q;21q) in a patient previously diagnosed as having monosomy 21. Clin Genet 1993;44:89-94.
-
(1993)
Clin Genet
, vol.44
, pp. 89-94
-
-
Hertz, B.1
Brandt, C.A.2
Petersen, M.B.3
-
15
-
-
0027326770
-
The origin of cytologically unidentifiable chromosome abnormalities: Six cases ascertained by targeted chromosome-band painting
-
Ohta T, Tohma T, Soejima H, et al. The origin of cytologically unidentifiable chromosome abnormalities: six cases ascertained by targeted chromosome-band painting. Hum Genet 1993;92:l-5.
-
(1993)
Hum Genet
, vol.92
-
-
Ohta, T.1
Tohma, T.2
Soejima, H.3
-
16
-
-
0020413177
-
Complex chromosomal rearrangements and their genetic consequences
-
Kleczkowska A, Fryns JP, Van den Berghe H. Complex chromosomal rearrangements and their genetic consequences. J Genet Hum 1982;30:199-214.
-
(1982)
J Genet Hum
, vol.30
, pp. 199-214
-
-
Kleczkowska, A.1
Fryns, J.P.2
Van Den Berghe, H.3
-
17
-
-
0023803572
-
Complex chromosomal rearrangement in a woman with multiple miscarriages
-
Kausch K, Haaf T, Köhler J, Schmid M. Complex chromosomal rearrangement in a woman with multiple miscarriages. Am J Med Genet 1988;31:415-20.
-
(1988)
Am J Med Genet
, vol.31
, pp. 415-420
-
-
Kausch, K.1
Haaf, T.2
Köhler, J.3
Schmid, M.4
-
18
-
-
0009723570
-
Collaborative U.S.A. data on prenatal diagnosis for parental carriers of chromosome rearrangements: Risks of unbalanced progeny
-
Daniel A, ed. New York: Alan R Liss
-
Daniel A, Hook EB, Wulf G. Collaborative U.S.A. data on prenatal diagnosis for parental carriers of chromosome rearrangements: risks of unbalanced progeny. In: Daniel A, ed. The cytogenetics of mammalian autosomal rearrangements. New York: Alan R Liss, 1988:101-2.
-
(1988)
The Cytogenetics of Mammalian Autosomal Rearrangements
, pp. 101-102
-
-
Daniel, A.1
Hook, E.B.2
Wulf, G.3
-
19
-
-
0027992380
-
Balanced complex chromosome rearrangement ascertained through prenatal diagnosis
-
Farrell SA, Summers AM, Gardner HA, Uchida IA. Balanced complex chromosome rearrangement ascertained through prenatal diagnosis. Am J Med Genet 1994;52:360-1.
-
(1994)
Am J Med Genet
, vol.52
, pp. 360-361
-
-
Farrell, S.A.1
Summers, A.M.2
Gardner, H.A.3
Uchida, I.A.4
-
20
-
-
0028124418
-
Complex chromosomal rearrangements: Some breakpoints may have cellular adaptive significance
-
Lurie IW, Wulfsberg EA, Prabhakar G, Rosenblum-Vos LS, Supovitz KR, Cohen MM. Complex chromosomal rearrangements: some breakpoints may have cellular adaptive significance. Clin Genet 1994;46:244-7.
-
(1994)
Clin Genet
, vol.46
, pp. 244-247
-
-
Lurie, I.W.1
Wulfsberg, E.A.2
Prabhakar, G.3
Rosenblum-Vos, L.S.4
Supovitz, K.R.5
Cohen, M.M.6
-
21
-
-
0018932911
-
The 11q;22q translocation: A European collaborative analysis of 43 cases
-
Fraccaro M, Lindsten J, Ford CE, Iselius L. The 11q;22q translocation: a European collaborative analysis of 43 cases. Hum Genet 1980;56:21-51.
-
(1980)
Hum Genet
, vol.56
, pp. 21-51
-
-
Fraccaro, M.1
Lindsten, J.2
Ford, C.E.3
Iselius, L.4
-
22
-
-
0019522231
-
Incomplete trisomy 22.1. Familial 11/22 translocation with 3:1 meiotic disjunction. Delineation of a common clinical picture and report of nine new cases from six families
-
Schinzel A, Schmid W, Auf der Maur P, et al. Incomplete trisomy 22.1. Familial 11/22 translocation with 3:1 meiotic disjunction. Delineation of a common clinical picture and report of nine new cases from six families. Hum Genet 1981;56:249-62.
-
(1981)
Hum Genet
, vol.56
, pp. 249-262
-
-
Schinzel, A.1
Schmid, W.2
Auf Der Maur, P.3
-
23
-
-
0019135082
-
Site-specific reciprocal translocation, t(11;22)(q23;q11) in several unrelated families with 3:1 meiotic disjuction
-
Zackai E, Emanuel B. Site-specific reciprocal translocation, t(11;22)(q23;q11) in several unrelated families with 3:1 meiotic disjuction. Am J Med Genet 1980;7:507-21.
-
(1980)
Am J Med Genet
, vol.7
, pp. 507-521
-
-
Zackai, E.1
Emanuel, B.2
-
25
-
-
0020576341
-
The 11q;22q translocation: A collaborative study of 20 new cases and analysis of 110 families
-
Iselius L, Lindstein J, Aurias A, et al. The 11q;22q translocation: a collaborative study of 20 new cases and analysis of 110 families. Hum Genet 1983;64:343-55.
-
(1983)
Hum Genet
, vol.64
, pp. 343-355
-
-
Iselius, L.1
Lindstein, J.2
Aurias, A.3
-
26
-
-
0029168062
-
Prenatal diagnosis of partial trisomy through in situ hybridization on amniocytes with whole chromosome and centromere-specific DNA probes. A case report
-
Blancato JK, Eglinton G, George J, Benkendorf J, Pinkert T, Aleck J. Prenatal diagnosis of partial trisomy through in situ hybridization on amniocytes with whole chromosome and centromere-specific DNA probes. A case report. J Reprod Med 1995;40:537-9.
-
(1995)
J Reprod Med
, vol.40
, pp. 537-539
-
-
Blancato, J.K.1
Eglinton, G.2
George, J.3
Benkendorf, J.4
Pinkert, T.5
Aleck, J.6
|