395 related articles for article (PubMed ID: 23817307)
1. A complex chromosome rearrangement involving four chromosomes, nine breakpoints and a cryptic 0.6-Mb deletion in a boy with cerebellar hypoplasia and defects in skull ossification.
Guilherme RS; Cernach MC; Sfakianakis TE; Takeno SS; Nardozza LM; Rossi C; Bhatt SS; Liehr T; Melaragno MI
Cytogenet Genome Res; 2013; 141(4):317-23. PubMed ID: 23817307
[TBL] [Abstract][Full Text] [Related]
2. De novo balanced complex chromosome rearrangement (CCR) involving chromosome 8, 11 and 16 in a boy with mild developmental delay and psychotic disorder.
Goumy C; Mihaescu M; Tchirkov A; Giollant M; Benier C; Francannet C; Jaffray JY; Geneix A; Vago P
Genet Couns; 2006; 17(3):371-9. PubMed ID: 17100206
[TBL] [Abstract][Full Text] [Related]
3. Molecular cytogenetic characterization of a constitutional complex intrachromosomal 4q rearrangement in a patient with multiple congenital anomalies.
Thienpont B; Gewillig M; Fryns JP; Devriendt K; Vermeesch J
Cytogenet Genome Res; 2006; 114(3-4):338-41. PubMed ID: 16954676
[TBL] [Abstract][Full Text] [Related]
4. Unbalanced inherited complex chromosome rearrangement involving chromosome 8, 10, 11 and 16 in a patient with congenital malformations and delayed development.
Karmous-Benailly H; Giuliano F; Massol C; Bloch C; De Ricaud D; Lambert JC; Perelman S
Eur J Med Genet; 2006; 49(5):431-8. PubMed ID: 16497571
[TBL] [Abstract][Full Text] [Related]
5. Familial complex chromosomal rearrangement resulting in a recombinant chromosome.
Berend SA; Bodamer OA; Shapira SK; Shaffer LG; Bacino CA
Am J Med Genet; 2002 May; 109(4):311-7. PubMed ID: 11992486
[TBL] [Abstract][Full Text] [Related]
6. FISH analysis of a complex chromosome rearrangement involving nine breakpoints on chromosomes 6, 12, 14 and 16.
Phelan MC; Blackburn W; Rogers RC; Crawford EC; Cooley NR; Schrock E; Ning Y; Ried T
Prenat Diagn; 1998 Nov; 18(11):1174-80. PubMed ID: 9854728
[TBL] [Abstract][Full Text] [Related]
7. Prenatal diagnosis of a de novo complex chromosome rearrangement (CCR) mediated by six breakpoints, and a review of 20 prenatally ascertained CCRs.
Giardino D; Corti C; Ballarati L; Finelli P; Valtorta C; Botta G; Giudici M; Grosso E; Larizza L
Prenat Diagn; 2006 Jun; 26(6):565-70. PubMed ID: 16683274
[TBL] [Abstract][Full Text] [Related]
8. Cytogenetic, FISH and array-CGH characterization of a complex chromosomal rearrangement carried by a mentally and language impaired patient.
Ballarati L; Recalcati MP; Bedeschi MF; Lalatta F; Valtorta C; Bellini M; Finelli P; Larizza L; Giardino D
Eur J Med Genet; 2009; 52(4):218-23. PubMed ID: 19236961
[TBL] [Abstract][Full Text] [Related]
9. Array CGH detection of a novel cryptic deletion at 3q13 in a complex chromosome rearrangement.
López-Expósito I; Ballesta-Martinez MJ; Bafalliu JA; Vera-Carbonell A; Domingo-Jiménez R; López-González V; Fernández A; Guillén-Navarro E
Genomics; 2014 Apr; 103(4):288-91. PubMed ID: 24607569
[TBL] [Abstract][Full Text] [Related]
10. Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.
Chen CP; Chern SR; Lee CC; Lin CC; Li YC; Hsieh LJ; Chen WL; Wang W
Prenat Diagn; 2006 Feb; 26(2):138-46. PubMed ID: 16470734
[TBL] [Abstract][Full Text] [Related]
11. Complex Rearrangement Involving Three Chromosomes, Four Breakpoints and a 2.7-Mb Deletion in the 18q Segment Observed in a Girl with Mild Learning Difficulties.
Kontodiou M; Daskalakis G; Vetro A; Paspaliaris V; Papaioannou G; Dagklis T; Tsakiridis I; Ziegler M; Liehr T; Thomaidis L; Papoulidis I; Manolakos E
Cytogenet Genome Res; 2015; 147(2-3):118-23. PubMed ID: 26681178
[TBL] [Abstract][Full Text] [Related]
12. A 6Mb deletion in band 2q22 due to a complex chromosome rearrangement associated with severe psychomotor retardation, microcephaly and distinctive dysmorphic facial features.
Hoffer MJ; Hilhorst-Hofstee Y; Knijnenburg J; Hansson KB; Engelberts AC; Laan LA; Bakker E; Rosenberg C
Eur J Med Genet; 2007; 50(2):149-54. PubMed ID: 17223398
[TBL] [Abstract][Full Text] [Related]
13. Array CGH detection of a cryptic deletion in a complex chromosome rearrangement.
Rosenberg C; Knijnenburg J; Chauffaille Mde L; Brunoni D; Catelani AL; Sloos W; Szuhai K; Tanke HJ
Hum Genet; 2005 Apr; 116(5):390-4. PubMed ID: 15726417
[TBL] [Abstract][Full Text] [Related]
14. De novo complex chromosome rearrangement: a study of two patients.
Melo DG; Huber J; Giuliani LR; Mazzucatto LF; Riegel M; Pina-Neto JM
Genet Couns; 2004; 15(3):303-10. PubMed ID: 15517822
[TBL] [Abstract][Full Text] [Related]
15. Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.
Caliskan MO; Karauzum SB; Mihci E; Tacoy S; Luleci G
Genet Couns; 2005; 16(2):129-38. PubMed ID: 16080292
[TBL] [Abstract][Full Text] [Related]
16. [Cytogenetic-molecular analysis of balanced chromosomal rearrangements in nine patients with intellectual disability, dysmorphic features and congenital abnormalities].
Borg K; Bocian E; Stankiewicz P; Obersztyn E; Kruczek A; Nowakowska B; Ilnicka A; Mazurczak T
Med Wieku Rozwoj; 2006; 10(1 Pt 2):227-46. PubMed ID: 17028391
[TBL] [Abstract][Full Text] [Related]
17. A 5q12.1-5q12.3 microdeletion in a case with a balanced exceptional complex chromosomal rearrangement.
Cetin Z; Yakut S; Clark OA; Mihci E; Berker S; Luleci G
Gene; 2013 Mar; 516(1):176-80. PubMed ID: 23262338
[TBL] [Abstract][Full Text] [Related]
18. An exceptional complex chromosomal rearrangement (CCR) with eight breakpoints involving four chromosomes (1;3;9;14) in an azoospermic male with normal phenotype.
Bartels I; Starke H; Argyriou L; Sauter SM; Zoll B; Liehr T
Eur J Med Genet; 2007; 50(2):133-8. PubMed ID: 17174164
[TBL] [Abstract][Full Text] [Related]
19. [Genetic analysis of a complex chromosome rearrangement involving two chromosomes and four breakpoints in an azoospermic man].
Luo YQ; Shen M; Qian YL; Chen YL; Xu CM; Jin F
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Apr; 26(2):200-2. PubMed ID: 19350516
[TBL] [Abstract][Full Text] [Related]
20. Cryptic genomic imbalances in de novo and inherited apparently balanced chromosomal rearrangements: array CGH study of 47 unrelated cases.
Schluth-Bolard C; Delobel B; Sanlaville D; Boute O; Cuisset JM; Sukno S; Labalme A; Duban-Bedu B; Plessis G; Jaillard S; Dubourg C; Henry C; Lucas J; Odent S; Pasquier L; Copin H; Latour P; Cordier MP; Nadeau G; Till M; Edery P; Andrieux J
Eur J Med Genet; 2009; 52(5):291-6. PubMed ID: 19505601
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
