-
1
-
-
79958752005
-
Complex chromosomal rearrangements: Origin and meiotic behavior
-
Pellestor F, Anahory T, Lefort G, et al. Complex chromosomal rearrangements: origin and meiotic behavior. Hum Reprod Update 2011 ; 17 : 476-494.
-
(2011)
Hum Reprod Update
, vol.17
, pp. 476-494
-
-
Pellestor, F.1
Anahory, T.2
Lefort, G.3
-
2
-
-
0020413177
-
Complex chromosomal rearrangements (CCR) and their genetic consequences
-
Kleczkowska A, Fryns JP, Van den Berghe H. Complex chromosomal rearrangements (CCR) 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
-
3
-
-
0023180029
-
Complex chromosome rearrangements and congenital anomalies
-
Kousseff BG, Nichols P, Essig YP, et al. Complex chromosome rearrangements and congenital anomalies. Am J Med Genet 1987 ; 26 : 771-782.
-
(1987)
Am J Med Genet
, vol.26
, pp. 771-782
-
-
Kousseff, B.G.1
Nichols, P.2
Essig, Y.P.3
-
4
-
-
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 : 415-420.
-
(1988)
Am J Med Genet
, vol.31
, pp. 415-420
-
-
Kausch, K.1
Haaf, T.2
Köhler, J.3
Schmid, M.4
-
5
-
-
0042823383
-
Ten years follow up of a boy with a complex chromosomal rearrangement: Going from a > 5 to 15-breakpoint CCR
-
Houge G, Liehr T, Schoumans J, et al. Ten years follow up of a boy with a complex chromosomal rearrangement: going from a > 5 to 15-breakpoint CCR. Am J Med Genet 2003 ; 118 : 235-240.
-
(2003)
Am J Med Genet
, vol.118
, pp. 235-240
-
-
Houge, G.1
Liehr, T.2
Schoumans, J.3
-
6
-
-
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 AWM, Van Bever Y. 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 1997 ; 99 : 806-815.
-
(1997)
Hum Genet
, vol.99
, pp. 806-815
-
-
Madan, K.1
Nieuwint, A.W.M.2
Van Bever, Y.3
-
7
-
-
84858998712
-
Balanced complex chromosome rearrangements: Reproductive aspects. A review
-
Madan K. Balanced complex chromosome rearrangements: reproductive aspects. A review. Am J Med Genet 2012 ; 158 : 947-963.
-
(2012)
Am J Med Genet
, vol.158
, pp. 947-963
-
-
Madan, K.1
-
8
-
-
1542790007
-
A complex chromosomal rearrangement with a translocation 4 10;14 in a fertile male carrier: Ascertainment through an offspring with partial trisomy 14q24-1q22 and partial monosomy 4q27-q28
-
Grasshoff U, Singer S, Liehr T, et al. A complex chromosomal rearrangement with a translocation 4;10;14 in a fertile male carrier: ascertainment through an offspring with partial trisomy 14q24-1q22 and partial monosomy 4q27-q28. Cytogenet Genome Res 2003 ; 103 : 17-23.
-
(2003)
Cytogenet Genome Res
, vol.103
, pp. 17-23
-
-
Grasshoff, U.1
Singer, S.2
Liehr, T.3
-
9
-
-
67649130683
-
Further delineation of complex chromosomal rearrangements in fertile male using multicolour banding
-
Karadeniz A, Mrasek K, Weise A. Further delineation of complex chromosomal rearrangements in fertile male using multicolour banding. Mol Cytogenet 2008 ; 1 : 17.
-
(2008)
Mol Cytogenet
, vol.1
, pp. 17
-
-
Karadeniz, A.1
Mrasek, K.2
Weise, A.3
-
10
-
-
77951731249
-
Insertional translocation detected using FISH confirmation or array-comparative genomic hybridization (aCGH) results
-
Kang SH, Shaw C, Ou Z, et al. Insertional translocation detected using FISH confirmation or array-comparative genomic hybridization (aCGH) results. Am J Med Genet 2010 ; 152 : 1111-1126.
-
(2010)
Am J Med Genet
, vol.152
, pp. 1111-1126
-
-
Kang, S.H.1
Shaw, C.2
Ou, Z.3
-
11
-
-
83655201192
-
Characterising chromosome rearrangements: Recent technical advances in molecular cytogenetics
-
Le Scouarnec S, Gribble SM. Characterising chromosome rearrangements: recent technical advances in molecular cytogenetics. Heredity 2012 ; 108 : 75-85.
-
(2012)
Heredity
, vol.108
, pp. 75-85
-
-
Le Scouarnec, S.1
Gribble, S.M.2
-
12
-
-
74949107557
-
Array painting: A protocol for the rapid analysis of aberrant chromosomes using DNA microarrays
-
Gribble SM, Ng BL, Prigmore E, et al. Array painting: a protocol for the rapid analysis of aberrant chromosomes using DNA microarrays. Nat Protoc 2009 ; 4 : 1722-1736.
-
(2009)
Nat Protoc
, vol.4
, pp. 1722-1736
-
-
Gribble, S.M.1
Ng, B.L.2
Prigmore, E.3
-
13
-
-
73949129010
-
Array-CGH detection of three cryptic submicroscopic imbalances in a complex chromosome rearrangement
-
Zhang F, Dai Y, Tu Z, et al. Array-CGH detection of three cryptic submicroscopic imbalances in a complex chromosome rearrangement. J Genet 2009 ; 88 : 369-372.
-
(2009)
J Genet
, vol.88
, pp. 369-372
-
-
Zhang, F.1
Dai, Y.2
Tu, Z.3
-
14
-
-
78049257955
-
The conundrum of a jumping translocation (JT) in CVS from twins and review of JTs
-
Reddy KS. The conundrum of a jumping translocation (JT) in CVS from twins and review of JTs. Am J Med Genet 2010 ; 152 : 2924-2936.
-
(2010)
Am J Med Genet
, vol.152
, pp. 2924-2936
-
-
Reddy, K.S.1
-
15
-
-
17144375306
-
Array CGH detection of a cryptic deletion in a complex chromosome rearrangement
-
Rosenberg C, Knijnenburg J, Chauffaille M, et al. Array CGH detection of a cryptic deletion in a complex chromosome rearrangement. Hum Genet 2005 ; 116 : 390-394.
-
(2005)
Hum Genet
, vol.116
, pp. 390-394
-
-
Rosenberg, C.1
Knijnenburg, J.2
Chauffaille, M.3
-
16
-
-
66749169417
-
Chromosome instability is common in human cleavage-stage embryos
-
Vanneste E, Voet T, Le Caignec C, et al. Chromosome instability is common in human cleavage-stage embryos. Nat Med 2009 ; 15 : 577-583.
-
(2009)
Nat Med
, vol.15
, pp. 577-583
-
-
Vanneste, E.1
Voet, T.2
Le Caignec, C.3
-
17
-
-
26244464073
-
Meiotic spindle checkpoints for assessment of aneuploidy oocytes
-
Steuerwald N. Meiotic spindle checkpoints for assessment of aneuploidy oocytes. Cytogenet Genome Res 2005 ; 111 : 256-259.
-
(2005)
Cytogenet Genome Res
, vol.111
, pp. 256-259
-
-
Steuerwald, N.1
-
18
-
-
76749171752
-
Mechanisms of chromosomal rearrangement in the human genome
-
Tsai AG, Lieber MR., Mechanisms of chromosomal rearrangement in the human genome. BMC Genomics 2010 ; 11 : S1.
-
(2010)
BMC Genomics
, vol.11
-
-
Tsai, A.G.1
Lieber, M.R.2
-
19
-
-
34547664096
-
Genomic disorders: Molecular mechanisms for rearrangements, conveyed phenotypes
-
Lupski JR, Stankiewicz P., Genomic disorders: molecular mechanisms for rearrangements, conveyed phenotypes. PLoS Genet 2005 ; 1 : e49.
-
(2005)
PLoS Genet
, vol.1
-
-
Lupski, J.R.1
Stankiewicz, P.2
-
21
-
-
54849404458
-
MMEJ repair of double-strand breaks (director's cut): Deleted sequences and alternative ending
-
McVey M, Lee SE. MMEJ repair of double-strand breaks (director's cut): deleted sequences and alternative ending. Trends Genet 2008 ; 24 : 529-538.
-
(2008)
Trends Genet
, vol.24
, pp. 529-538
-
-
McVey, M.1
Lee, S.E.2
-
22
-
-
84860203870
-
Multiple cellular mechanisms prevent chromosomal rearrangements involving repetitive DNA
-
George CM, Alani E. Multiple cellular mechanisms prevent chromosomal rearrangements involving repetitive DNA. Critic Rev Biochem Mol Biol 2012 ; 47 : 297-313.
-
(2012)
Critic Rev Biochem Mol Biol
, vol.47
, pp. 297-313
-
-
George, C.M.1
Alani, E.2
-
23
-
-
77956849313
-
Genomic rearrangements in inherited disease and cancer
-
Chen JM, Cooper DN, Férec C, et al. Genomic rearrangements in inherited disease and cancer. Semin Cancer Biol 2010 ; 20 : 222-233.
-
(2010)
Semin Cancer Biol
, vol.20
, pp. 222-233
-
-
Chen, J.M.1
Cooper, D.N.2
Férec, C.3
-
24
-
-
37349109667
-
A DNA replication mechanism for generating nonrecurrent rearrangements associated with genomic disorders
-
Lee JA, Carvalho CM, Lupski JR. A DNA replication mechanism for generating nonrecurrent rearrangements associated with genomic disorders. Cell 2007 ; 131 : 1235-1247.
-
(2007)
Cell
, vol.131
, pp. 1235-1247
-
-
Lee, J.A.1
Carvalho, C.M.2
Lupski, J.R.3
-
25
-
-
59249105978
-
A microhomology-mediated break-induced replication model for the origin of human copy number variation
-
Hastings PJ, Ira G, Lupski JR. A microhomology-mediated break-induced replication model for the origin of human copy number variation. PLoS Genet 2009 ; 5 : e1000327.
-
(2009)
PLoS Genet
, vol.5
-
-
Hastings, P.J.1
Ira, G.2
Lupski, J.R.3
-
26
-
-
34247611513
-
Template switching during break-Induced replication
-
Smith CE, Llorente B, Symington LS. Template switching during break-Induced replication. Nature 2007 ; 447 : 102-105.
-
(2007)
Nature
, vol.447
, pp. 102-105
-
-
Smith, C.E.1
Llorente, B.2
Symington, L.S.3
-
27
-
-
67649557486
-
Recent advance in our understanding of the molecular nature of chromosomal abnormalities
-
Kurahashi H, Bolor H, Kato T, et al. Recent advance in our understanding of the molecular nature of chromosomal abnormalities. J Hum Genet 2009 ; 54 : 253-260.
-
(2009)
J Hum Genet
, vol.54
, pp. 253-260
-
-
Kurahashi, H.1
Bolor, H.2
Kato, T.3
-
28
-
-
77954700065
-
Biological roles of translin and translin-associated factor-X: RNA metabolism comes to the fore
-
Jaendling A, McFarlane RJ. Biological roles of translin and translin-associated factor-X: RNA metabolism comes to the fore. Biochem J 2010 ; 429 : 225-234.
-
(2010)
Biochem J
, vol.429
, pp. 225-234
-
-
Jaendling, A.1
McFarlane, R.J.2
-
29
-
-
0035316574
-
Chromosome territories, nuclear architecture and gene regulation in mammalian cells
-
Cremer T, Cremer C. Chromosome territories, nuclear architecture and gene regulation in mammalian cells. Nat Rev Genet 2001 ; 2 : 292-301.
-
(2001)
Nat Rev Genet
, vol.2
, pp. 292-301
-
-
Cremer, T.1
Cremer, C.2
-
30
-
-
5444243359
-
Active genes dynamically colocalize to shared sites of ongoing transcription
-
Osborne CS, Chakalova L, Brown KE, et al. Active genes dynamically colocalize to shared sites of ongoing transcription. Nat Genet 2004 ; 36 : 1065-1071.
-
(2004)
Nat Genet
, vol.36
, pp. 1065-1071
-
-
Osborne, C.S.1
Chakalova, L.2
Brown, K.E.3
-
31
-
-
0034747032
-
HC Forum: A web site based on an international human cytogenetic database
-
Cohen O, Mermet MA, Demongeot J. HC Forum: a web site based on an international human cytogenetic database. Nucleic Acids Res 2001 ; 29 : 305-307.
-
(2001)
Nucleic Acids Res
, vol.29
, pp. 305-307
-
-
Cohen, O.1
Mermet, M.A.2
Demongeot, J.3
-
32
-
-
19944370510
-
Complex chromosome rearrangement and recombinant balanced translocation in a mother and a daughter with the same phenotypic abnormalities
-
Tihy F, Lemieux N, Lemyre E. Complex chromosome rearrangement and recombinant balanced translocation in a mother and a daughter with the same phenotypic abnormalities. Am J Med Genet 2005 ; 135 : 317-319.
-
(2005)
Am J Med Genet
, vol.135
, pp. 317-319
-
-
Tihy, F.1
Lemieux, N.2
Lemyre, E.3
-
33
-
-
0034969830
-
Study of the occurrence of interchromosomal effect in spermatozoa of chromosomal rearrangement carriers by fluorescence in situ hybridization and primed in situ labeling techniques
-
Pellestor F, Imbert I, Andréo B, et al. Study of the occurrence of interchromosomal effect in spermatozoa of chromosomal rearrangement carriers by fluorescence in situ hybridization and primed in situ labeling techniques. Hum Reprod 2001 ; 16 : 1155-1164.
-
(2001)
Hum Reprod
, vol.16
, pp. 1155-1164
-
-
Pellestor, F.1
Imbert, I.2
Andréo, B.3
-
34
-
-
0031425426
-
Lack of checkpoint control at the metaphase/anaphase transitiion: A mechanism of meiotic nondisjunction in mammalian females
-
LeMaire-Adkins R, Radke K, Hunt PA. Lack of checkpoint control at the metaphase/anaphase transitiion: a mechanism of meiotic nondisjunction in mammalian females. J Cell Biol 1997 ; 139 : 1611-1619.
-
(1997)
J Cell Biol
, vol.139
, pp. 1611-1619
-
-
Lemaire-Adkins, R.1
Radke, K.2
Hunt, P.A.3
-
35
-
-
0031242638
-
Assisted reproductive technology and complex chromosomal rearrangements: The limites of ICSI
-
Siffroi JP, Benzacken B, Straub B, et al. Assisted reproductive technology and complex chromosomal rearrangements: the limites of ICSI. Mol Hum Reprod 1997 ; 3 : 847-851.
-
(1997)
Mol Hum Reprod
, vol.3
, pp. 847-851
-
-
Siffroi, J.P.1
Benzacken, B.2
Straub, B.3
-
36
-
-
55149097693
-
A healthy live birth after successful preimplantation genetic diagnosis for carriers of complex chromosome rearrangements
-
Lim CK, Cho JW, Kim JY, et al. A healthy live birth after successful preimplantation genetic diagnosis for carriers of complex chromosome rearrangements. Fertil Steril 2008 ; 90 : 1680-1684.
-
(2008)
Fertil Steril
, vol.90
, pp. 1680-1684
-
-
Lim, C.K.1
Cho, J.W.2
Kim, J.Y.3
-
37
-
-
79952838990
-
PGD for a complex chromosomal rearrangement by array comparative genomic hybridization
-
Vanneste E, Melotte C, Voet T, et al. PGD for a complex chromosomal rearrangement by array comparative genomic hybridization. Hum Reprod 2011 ; 26 : 941-949.
-
(2011)
Hum Reprod
, vol.26
, pp. 941-949
-
-
Vanneste, E.1
Melotte, C.2
Voet, T.3
-
38
-
-
84856598589
-
La théorie de l'équilibre ponctué
-
Reynaud C, Billaud M. La théorie de l'équilibre ponctué. Med Sci (Paris) 2011 ; 27 : 921-923.
-
(2011)
Med Sci (Paris)
, vol.27
, pp. 921-923
-
-
Reynaud, C.1
Billaud, M.2
-
39
-
-
78650959663
-
Massive genomic rearrangement acquired in a single catastrophic event during cancer development
-
Stephens PJ, Greenman CD, Fu B, et al. Massive genomic rearrangement acquired in a single catastrophic event during cancer development. Cell 2011 ; 144 : 27-40.
-
(2011)
Cell
, vol.144
, pp. 27-40
-
-
Stephens, P.J.1
Greenman, C.D.2
Fu, B.3
-
40
-
-
84863105790
-
Constitutional chromothripsis rearrangements involve clustered double-stranded DNA breaks and nonhomologous repair mechnisms
-
Klosterman WP, Tavakoli-Yaraki M, Van Roosmalen M, et al. Constitutional chromothripsis rearrangements involve clustered double-stranded DNA breaks and nonhomologous repair mechnisms. Cell Rep 2012 ; 1 : 648-655.
-
(2012)
Cell Rep
, vol.1
, pp. 648-655
-
-
Klosterman, W.P.1
Tavakoli-Yaraki, M.2
Van Roosmalen, M.3
-
41
-
-
1042302927
-
SPO11 : une activité de coupure de l'ADN indispensable à la méiose
-
Baudat F, de Massy B. SPO11 : une activité de coupure de l'ADN indispensable à la méiose. Med Sci (Paris) 2004 ; 20 : 213-218.
-
(2004)
Med Sci (Paris)
, vol.20
, pp. 213-218
-
-
Baudat, F.1
De Massy, B.2
-
42
-
-
84875650883
-
Fonction des suppresseurs de tumeur PALB2 et BRCA2 dans la réparation des cassures double-brin de l'ADN
-
Buisson R, Masson JY. Fonction des suppresseurs de tumeur PALB2 et BRCA2 dans la réparation des cassures double-brin de l'ADN. Med Sci (Paris) 2013 ; 29 : 301-307.
-
(2013)
Med Sci (Paris)
, vol.29
, pp. 301-307
-
-
Buisson, R.1
Masson, J.Y.2
-
43
-
-
84861917862
-
Génétique de l'infertilité masculine : les nouveaux acteurs
-
Coutton C, Satre V, Arnoult C, Ray P. Génétique de l'infertilité masculine : les nouveaux acteurs. Med Sci (Paris) 2012 ; 28 : 497-502.
-
(2012)
Med Sci (Paris)
, vol.28
, pp. 497-502
-
-
Coutton, C.1
Satre, V.2
Arnoult, C.3
Ray, P.4
-
44
-
-
84884629931
-
Instabilité chromosomique et cancer enfin des CIN révélateurs
-
Le Borgne M, Chartier N, Billaud M. Instabilité chromosomique et cancer, enfin des CIN révélateurs. Med Sci (Paris) 2013 ; 29 : 807-810.
-
(2013)
Med Sci (Paris)
, vol.29
, pp. 807-810
-
-
Le Borgne, M.1
Chartier, N.2
Billaud, M.3
|