-
1
-
-
2542482661
-
Delineation of complex chromosomal rearrangements: Evidence for increased complexity
-
Astbury C, Christ LA, Aughton DJ, et al. 2004. Delineation of complex chromosomal rearrangements: evidence for increased complexity. Hum Genet 114: 448-457.
-
(2004)
Hum Genet
, vol.114
, pp. 448-457
-
-
Astbury, C.1
Christ, L.A.2
Aughton, D.J.3
-
2
-
-
0035287956
-
Prenatal diagnosis of de novo complex balanced rearrangements in chromosomes 3, 4 and 13
-
Balicek P, Juttnerova V, Jarosova M, Fialova J, Fiedler Z, Kolmanova J. 2001. Prenatal diagnosis of de novo complex balanced rearrangements in chromosomes 3, 4 and 13. Cas Lek Cesk 140: 122-124.
-
(2001)
Cas Lek Cesk
, vol.140
, pp. 122-124
-
-
Balicek, P.1
Juttnerova, V.2
Jarosova, M.3
Fialova, J.4
Fiedler, Z.5
Kolmanova, J.6
-
3
-
-
0028043602
-
Molecular analysis of a complex chromosomal rearrangement and a review of familial cases
-
Batista DAS, Pai GS, Stetten G. 1994. Molecular analysis of a complex chromosomal rearrangement and a review of familial cases. Am J Med Genet 53: 255-263.
-
(1994)
Am J Med Genet
, vol.53
, pp. 255-263
-
-
Das, B.1
Pai, G.S.2
Stetten, G.3
-
4
-
-
0027202605
-
A complex chromosomal rearrangement detected prenatally and studied by fluorescence in situ hybridization
-
Batista DAS, Tuck-Muller CM, Martinez JE, Kearns WG, Pearson PL, Stetten G. 1993. A complex chromosomal rearrangement detected prenatally and studied by fluorescence in situ hybridization. Hum Genet 92: 117-121.
-
(1993)
Hum Genet
, vol.92
, pp. 117-121
-
-
Batista, D.A.S.1
Tuck-Muller, C.M.2
Martinez, J.E.3
Kearns, W.G.4
Pearson, P.L.5
Stetten, G.6
-
5
-
-
0008615113
-
Three prenatal diagnoses of complex chromosome rearrangements
-
Bellec V, de Perdigo A. 1991. Three prenatal diagnoses of complex chromosome rearrangements. Am J Hum Genet 49: 256.
-
(1991)
Am J Hum Genet
, vol.49
, pp. 256
-
-
Bellec, V.1
De Perdigo, A.2
-
6
-
-
0022577294
-
Prenatal diagnosis and follow-up of a child with a complex chromosome rearrangement
-
Bogart MH, Bradshaw CL, Jones OW, Schanberger JE. 1986. Prenatal diagnosis and follow-up of a child with a complex chromosome rearrangement. J Med Genet 23: 180-183.
-
(1986)
J Med Genet
, vol.23
, pp. 180-183
-
-
Bogart, M.H.1
Bradshaw, C.L.2
Jones, O.W.3
Schanberger, J.E.4
-
7
-
-
1842428731
-
Two unusual chromosome aberrations ascertained by sonographic anomalies
-
Bourthoumieu S, Esclaire F, Terro F, et al. 2004. Two unusual chromosome aberrations ascertained by sonographic anomalies. Prenat Diagn 24: 219-223.
-
(2004)
Prenat Diagn
, vol.24
, pp. 219-223
-
-
Bourthoumieu, S.1
Esclaire, F.2
Terro, F.3
-
8
-
-
0028926835
-
Fetal translocation between chromosomes 2, 18 and 21 resolved by FISH
-
Delaroche I, Sabani M, Calabrese G, Mingarelli R, Palka G, Dallapiccola B. 1995. Fetal translocation between chromosomes 2, 18 and 21 resolved by FISH. Prenat Diagn 15: 278-281.
-
(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
-
9
-
-
0036071427
-
Heterozygous submicroscopic inversions involving olfactory receptor-gene clusters mediate the recurrent t(4;8)(p16;p23) translocation
-
Giglio S, Calvari V, Gregato G, et al. 2002. Heterozygous submicroscopic inversions involving olfactory receptor-gene clusters mediate the recurrent t(4;8)(p16;p23) translocation. Am J Hum Genet 71: 276-285.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 276-285
-
-
Giglio, S.1
Calvari, V.2
Gregato, G.3
-
10
-
-
19944432367
-
The complex nature of constitutional de novo apparently balanced translocations in patients presenting with abnormal phenotypes
-
Gribble SM, Prigmore E, Burford DC, et al. 2005. The complex nature of constitutional de novo apparently balanced translocations in patients presenting with abnormal phenotypes. J Med Genet 42: 8-16.
-
(2005)
J Med Genet
, vol.42
, pp. 8-16
-
-
Gribble, S.M.1
Prigmore, E.2
Burford, D.C.3
-
11
-
-
0022640683
-
Prenatal diagnosis of a de novo complex chromosomal rearrangement involving four chromosomes
-
Kim HJ, Perle MA, Bogosian V, Greco A. 1986. Prenatal diagnosis of a de novo complex chromosomal rearrangement involving four chromosomes. Prenat Diagn 6: 211-216.
-
(1986)
Prenat Diagn
, vol.6
, pp. 211-216
-
-
Kim, H.J.1
Perle, M.A.2
Bogosian, V.3
Greco, A.4
-
12
-
-
0022777234
-
Prenatal diagnosis of complex balanced rearrangement of chromosomes 7 and 14 in a healthy child with a history of preconceptual X-ray exposure
-
Kohler J, Brackertz M, Feige A, Grimm T. 1986. Prenatal diagnosis of complex balanced rearrangement of chromosomes 7 and 14 in a healthy child with a history of preconceptual X-ray exposure. Prenat Diagn 6: 389-391.
-
(1986)
Prenat Diagn
, vol.6
, pp. 389-391
-
-
Kohler, J.1
Brackertz, M.2
Feige, A.3
Grimm, T.4
-
13
-
-
0036192056
-
Prenatal diagnosis of a familial complex chromosomal rearrangement involving chromosomes 5, 10, 16 and 18
-
Lee MH, Park SY, Kim YM, et al. 2002. Prenatal diagnosis of a familial complex chromosomal rearrangement involving chromosomes 5, 10, 16 and 18. Prenat Diagn 22: 102-104.
-
(2002)
Prenat Diagn
, vol.22
, pp. 102-104
-
-
Lee, M.H.1
Park, S.Y.2
Kim, Y.M.3
-
14
-
-
0023692635
-
Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries
-
Lichter P, Cremer T, Borden J, Manuehdis L, Ward DC. 1988. Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries. Hum Genet 80: 224-234.
-
(1988)
Hum Genet
, vol.80
, pp. 224-234
-
-
Lichter, P.1
Cremer, T.2
Borden, J.3
Manuehdis, L.4
Ward, D.C.5
-
15
-
-
0030906960
-
Recombination in a balanced complex translocation of a mother leading to a balanced reciprocal translocation in the child. Review of 60 cases of balanced complex translocations
-
Madan K, Nieuwint AW, Bever Yvan. 1997. Recombination in a balanced complex translocation of a mother leading to a balanced reciprocal translocation in the child. Review of 60 cases of balanced complex translocations. Hum Genet 99: 806-815.
-
(1997)
Hum Genet
, vol.99
, pp. 806-815
-
-
Madan, K.1
Nieuwint, A.W.2
Yvan, B.3
-
16
-
-
0029811054
-
Molecular analysis by fluorescence in situ hybridization of a prenatally detected de novo complex chromosomal rearrangement t(2q;3p;4q;13q)
-
Mercier S, Fellmann F, Cattin J, Bresson JL. 1996. Molecular analysis by fluorescence in situ hybridization of a prenatally detected de novo complex chromosomal rearrangement t(2q;3p;4q;13q). Prenat Diagn 16: 1046-1050.
-
(1996)
Prenat Diagn
, vol.16
, pp. 1046-1050
-
-
Mercier, S.1
Fellmann, F.2
Cattin, J.3
Bresson, J.L.4
-
17
-
-
1842784007
-
Prenatal diagnosis of an extra der(4) resulting from a complex maternal chromosome translocation
-
Migliori MV, Pettinari A, Ciaschini AM, Piermattei P, Pigliapoco F, Discepoli G. 2004. Prenatal diagnosis of an extra der(4) resulting from a complex maternal chromosome translocation. Prenat Diagn 24: 290-292.
-
(2004)
Prenat Diagn
, vol.24
, pp. 290-292
-
-
Migliori, M.V.1
Pettinari, A.2
Ciaschini, A.M.3
Piermattei, P.4
Pigliapoco, F.5
Discepoli, G.6
-
18
-
-
0019121059
-
Complex chromosome rearrangements. Report of a new case and literature review
-
Pai GS, Thomas GH, Mahoney W, Migeon BR. 1980. Complex chromosome rearrangements. Report of a new case and literature review. Clin Genet 18: 436-444.
-
(1980)
Clin Genet
, vol.18
, pp. 436-444
-
-
Pai, G.S.1
Thomas, G.H.2
Mahoney, W.3
Migeon, B.R.4
-
19
-
-
0032730123
-
Analysis of a de novo complex chromosome rearrangement involving chromosomes 4, 11, 12 and 13 and eight breakpoints by conventional cytogenetic, fluorescence in situ hybridization and spectral karyotyping
-
Peschka B, Leygraaf J, Hansmann D, et al. 1999. Analysis of a de novo complex chromosome rearrangement involving chromosomes 4, 11, 12 and 13 and eight breakpoints by conventional cytogenetic, fluorescence in situ hybridization and spectral karyotyping. Prenat Diagn 19: 1143-1149.
-
(1999)
Prenat Diagn
, vol.19
, pp. 1143-1149
-
-
Peschka, B.1
Leygraaf, J.2
Hansmann, D.3
-
20
-
-
0031729663
-
FISH analysis of a complex chromosome rearrangement involving nine breakpoints on chromosomes 6, 12, 14 and 16
-
Phelan MC, Blackburn W, Rogers CR, et al. 1998. FISH analysis of a complex chromosome rearrangement involving nine breakpoints on chromosomes 6, 12, 14 and 16. Prenat Diagn 18: 1174-1180.
-
(1998)
Prenat Diagn
, vol.18
, pp. 1174-1180
-
-
Phelan, M.C.1
Blackburn, W.2
Rogers, C.R.3
-
21
-
-
0029789544
-
Prenatally diagnosed de novo apparently balanced complex chromosome rearrangements: Two new cases and review of the literature
-
Ruiz C, Grubs RE, Jewett T, et al. 1996. Prenatally diagnosed de novo apparently balanced complex chromosome rearrangements: two new cases and review of the literature. Am J Med Genet 64: 478-484.
-
(1996)
Am J Med Genet
, vol.64
, pp. 478-484
-
-
Ruiz, C.1
Grubs, R.E.2
Jewett, T.3
-
22
-
-
0029021613
-
Prenatal diagnosis in two cases of de novo complex chromosomal rearrangements: Three year follow-up in one case
-
Sikkema-Raddatz B, Sijmons RH, Tan-Sindhunata MB, et al. 1995. Prenatal diagnosis in two cases of de novo complex chromosomal rearrangements: three year follow-up in one case. Prenat Diagn 15: 467-473.
-
(1995)
Prenat Diagn
, vol.15
, pp. 467-473
-
-
Sikkema-Raddatz, B.1
Sijmons, R.H.2
Tan-Sindhunata, M.B.3
-
23
-
-
16344391048
-
Recombination in a male carrier of two reciprocal translocations involving chromosomes 14, 140, 15, and 21 leading to balanced and unbalanced rearrangements in offspring
-
Soler A, Sànchez A, Carriö A, et al. 2005. Recombination in a male carrier of two reciprocal translocations involving chromosomes 14, 140, 15, and 21 leading to balanced and unbalanced rearrangements in offspring. Am J Med Genet 134A: 309-314.
-
(2005)
Am J Med Genet
, vol.134 A
, pp. 309-314
-
-
Soler, A.1
Sànchez, A.2
Carriö, A.3
-
24
-
-
0018318837
-
Prenatal diagnosis and postnatal follow-up of an abnormal child with two de novo apparently balanced translocations
-
Stoll C, Flori E, MacLear J, Renaud R. 1979. Prenatal diagnosis and postnatal follow-up of an abnormal child with two de novo apparently balanced translocations. Hum Genet 47: 221-224.
-
(1979)
Hum Genet
, vol.47
, pp. 221-224
-
-
Stoll, C.1
Flori, E.2
MacLear, J.3
Renaud, R.4
-
25
-
-
14844288095
-
Prenatal diagnosis and molecular cytogenetic characterization of an unusual complex structural rearrangement in a pregnancy following intracytoplasmic sperm injection (ICSI)
-
Trimborn M, Liehr T, Belitz B, et al. 2005. Prenatal diagnosis and molecular cytogenetic characterization of an unusual complex structural rearrangement in a pregnancy following intracytoplasmic sperm injection (ICSI). J Histochem Cytochem 53: 351-354.
-
(2005)
J Histochem Cytochem
, vol.53
, pp. 351-354
-
-
Trimborn, M.1
Liehr, T.2
Belitz, B.3
-
26
-
-
0025941775
-
De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: Clinical significance and distribution of breakpoints
-
Warburton D. 1991. De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints. Am J Hum Genet 49: 995-1013.
-
(1991)
Am J Hum Genet
, vol.49
, pp. 995-1013
-
-
Warburton, D.1
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