203 related articles for article (PubMed ID: 34607577)
1. A rare familial rearrangement of chromosomes 9 and 15 associated with intellectual disability: a clinical and molecular study.
Lemskaya NA; Romanenko SA; Rezakova MA; Filimonova EA; Prokopov DY; Dolskiy AA; Perelman PL; Maksimova YV; Shorina AR; Yudkin DV
Mol Cytogenet; 2021 Oct; 14(1):47. PubMed ID: 34607577
[TBL] [Abstract][Full Text] [Related]
2. A novel maternally-derived insertional translocation resulting in partial trisomy 4q13.2-q22.1 with complex translocation t(8;20) in a family with intellectual disability.
Assawamakin A; Wattanasirichaigoon D; Tocharoentanaphol C; Waeteekul S; Tansatit M; Thongnoppakhun W; Limwongse C
Am J Med Genet A; 2012 Apr; 158A(4):901-8. PubMed ID: 22419381
[TBL] [Abstract][Full Text] [Related]
3. Complex small supernumerary marker chromosome with a 15q/16p duplication: clinical implications.
Christofolini DM; Piazzon FB; Evo C; Mafra FA; Cosenza SR; Dias AT; Barbosa CP; Bianco B; Kulikowski LD
Mol Cytogenet; 2014; 7():29. PubMed ID: 24839463
[TBL] [Abstract][Full Text] [Related]
4. Two distinctive classic genetic syndromes, 22q11.2 deletion syndrome and Angelman syndrome, occurring within the same family.
Kosaki R; Migita O; Takahashi T; Kosaki K
Am J Med Genet A; 2009 Feb; 149A(4):702-5. PubMed ID: 19288551
[TBL] [Abstract][Full Text] [Related]
5. Array-CGH study of partial trisomy 9p without mental retardation.
Bouhjar IB; Hannachi H; Zerelli SM; Labalme A; Gmidène A; Soyah N; Missaoui S; Sanlaville D; Elghezal H; Saad A
Am J Med Genet A; 2011 Jul; 155A(7):1735-9. PubMed ID: 21626676
[TBL] [Abstract][Full Text] [Related]
6. A small (sSMC) chromosome 22 due to a maternal translocation between chromosomes 8 and 22: a case report.
Mundhofir FE; Kooper AJ; Winarni TI; Smits AP; Faradz SM; Hamel BC
Genet Couns; 2010; 21(1):99-108. PubMed ID: 20420036
[TBL] [Abstract][Full Text] [Related]
7. Rare partial octosomy and hexasomy of 15q11-q13 associated with intellectual impairment and development delay: report of two cases and review of literature.
Li H; Du J; Li W; Cheng D; He W; Yi D; Xiong B; Yuan S; Tu C; Meng L; Luo A; Lin G; Lu G; Tan YQ
Mol Cytogenet; 2018; 11():15. PubMed ID: 29441129
[TBL] [Abstract][Full Text] [Related]
8. Duplication of the 15q11-q13 region: clinical and genetic study of 30 new cases.
Al Ageeli E; Drunat S; Delanoë C; Perrin L; Baumann C; Capri Y; Fabre-Teste J; Aboura A; Dupont C; Auvin S; El Khattabi L; Chantereau D; Moncla A; Tabet AC; Verloes A
Eur J Med Genet; 2014 Jan; 57(1):5-14. PubMed ID: 24239951
[TBL] [Abstract][Full Text] [Related]
9. A de novo chromosome 9p duplication in a female child with short stature and developmental delay.
Tkemaladze T; Bregvadze K; Papiashvili N; Gagua S; Abzianidze E
SAGE Open Med Case Rep; 2023; 11():2050313X231160883. PubMed ID: 36968988
[TBL] [Abstract][Full Text] [Related]
10. Partial trisomy 9p and 14q microduplication in a patient with growth retardation: a case report and review of the literature.
Fan J; Zhou J; Lin D; Guo Y; Li S; Zhang S; Liang L; Yan L
J Pediatr Endocrinol Metab; 2020 Mar; 33(3):431-436. PubMed ID: 32069233
[TBL] [Abstract][Full Text] [Related]
11. Rare partial trisomy and tetrasomy of 15q11-q13 associated with developmental delay and autism spectrum disorder.
Lu Y; Liang Y; Ning S; Deng G; Xie Y; Song J; Zuo N; Feng C; Qin Y
Mol Cytogenet; 2020; 13():21. PubMed ID: 32536972
[TBL] [Abstract][Full Text] [Related]
12. Characterization of familial partial 10p trisomy by chromosomal microdissection, FISH, and microsatellite dosage analysis.
Stone D; Ning Y; Guan XY; Kaiser-Kupfer M; Wynshaw-Boris A; Biesecker L
Hum Genet; 1996 Oct; 98(4):396-402. PubMed ID: 8792811
[TBL] [Abstract][Full Text] [Related]
13. Co-existence of 9p deletion and Silver-Russell syndromes in a patient with maternally inherited cryptic complex chromosome rearrangement involving chromosomes 4, 9, and 11.
Hu J; Sathanoori M; Kochmar S; Madan-Khetarpal S; McGuire M; Surti U
Am J Med Genet A; 2013 Jan; 161A(1):179-84. PubMed ID: 23225375
[TBL] [Abstract][Full Text] [Related]
14. Trisomy 9p and Prader-Willi syndromes in an infant resulting from a de-novo unbalanced t(9;15) translocation.
Carter MT; Jacob FD; Sinclair-Bourque E; Ray R; Allanson JE
Clin Dysmorphol; 2009 Apr; 18(2):103-106. PubMed ID: 19282755
[TBL] [Abstract][Full Text] [Related]
15. Characterization of a Complex Chromosomal Rearrangement Involving a de novo Duplication of 9p and 9q and a Deletion of 9q.
Martín-De Saro MD; Valdés-Miranda JM; Plaza-Benhumea L; Pérez-Cabrera A; Gonzalez-Huerta LM; Guevara-Yañez R; Cuevas-Covarrubias SA
Cytogenet Genome Res; 2015; 147(2-3):124-9. PubMed ID: 26900692
[TBL] [Abstract][Full Text] [Related]
16. Prader-Willi syndrome resulting from an unbalanced translocation: characterization by array comparative genomic hybridization.
Klein OD; Cotter PD; Albertson DG; Pinkel D; Tidyman WE; Moore MW; Rauen KA
Clin Genet; 2004 Jun; 65(6):477-82. PubMed ID: 15151506
[TBL] [Abstract][Full Text] [Related]
17. Reciprocal translocation between the proximal regions of the long arms of chromosomes 13 and 15 resulting in unbalanced offspring: characterization by fluorescence in situ hybridization and DNA analysis.
Mangelschots K; Van Roy B; Speleman F; Van Roy N; Gheuens J; Beuten J; Buntinx I; Van Thienen MN; Willekens H; Dumon J
Hum Genet; 1992 Jun; 89(4):407-13. PubMed ID: 1352272
[TBL] [Abstract][Full Text] [Related]
18. Unbalanced translocation t(15;22) in "severe" Prader-Willi syndrome.
Smith A; Jauch A; St Heaps L; Robson L; Kearney B
Ann Genet; 2000; 43(3-4):125-30. PubMed ID: 11164193
[TBL] [Abstract][Full Text] [Related]
19. Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication.
Chen CP; Lin CJ; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Chen LF; Yang CW; Wang W
Taiwan J Obstet Gynecol; 2016 Aug; 55(4):596-601. PubMed ID: 27590390
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]