162 related articles for article (PubMed ID: 29896750)
1. [Genetic analysis of an infant with duplication 9q34 syndrome].
Tong Y; Yan S; Shi J; Chen L; Wan C; Xu K
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Jun; 35(3):437-439. PubMed ID: 29896750
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. [A case with partial trisomy 7 (q34→qter) derived from a paternal reciprocal translocation t(7;14)(q34;q32)].
Xiao B; Ji X; Jiang WT; Zhang JM; Hu Q; Tao J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Dec; 28(6):654-7. PubMed ID: 22161098
[TBL] [Abstract][Full Text] [Related]
4. Cryptic duplication and deletion of 9q34.3 --> qter in a family with a t(9;22)(q34.3;p11.2).
Sanger TM; Olney AH; Zaleski D; Pickering D; Nelson M; Sanger WG; Dave BJ
Am J Med Genet A; 2005 Sep; 138(1):51-5. PubMed ID: 16104013
[TBL] [Abstract][Full Text] [Related]
5. [Unbalanced subtelomic rearrangement involving 9q and 22q in a child with mental retardation and multiple congenital anomalies].
Xiao B; Xing Y; Ji X; Xu Y; Ni L; Zhu Y; Tao J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Dec; 30(6):666-9. PubMed ID: 24327143
[TBL] [Abstract][Full Text] [Related]
6. Double partial trisomy 9q34.1-->qter and 21pter-->q22.11: FISH and clinical findings.
Mattina T; Pierluigi M; Mazzone D; Scardilli S; Perfumo C; Mollica F
J Med Genet; 1997 Nov; 34(11):945-8. PubMed ID: 9391894
[TBL] [Abstract][Full Text] [Related]
7. Molecular cytogenetic studies of duplication 9q32-->q34.3 inserted into 9q13.
Hou JW; Wang TR
Clin Genet; 1995 Sep; 48(3):148-50. PubMed ID: 8556822
[TBL] [Abstract][Full Text] [Related]
8. Maternal balanced translocation leading to partial duplication of 4q and partial deletion of 1p in a son: cytogenetic and FISH studies using band-specific painting probes generated by chromosome microdissection.
Chen Z; Grebe TA; Guan XY; Notohamiprodjo M; Nutting PJ; Stone JF; Trent JM; Sandberg AA
Am J Med Genet; 1997 Aug; 71(2):160-6. PubMed ID: 9217215
[TBL] [Abstract][Full Text] [Related]
9. Pure 9p trisomy derived from a terminal balanced unreciprocal translocation.
Brambila-Tapia AJ; Neira VA; Vásquez-Velásquez AI; Jimenez-Arredondo RE; Chávez-González EL; Picos-Cárdenas VJ; Fletes-Rayas AL; Figuera LE
Genet Couns; 2014; 25(3):289-97. PubMed ID: 25365851
[TBL] [Abstract][Full Text] [Related]
10. A dysmorphic newborn infant with a complex rearrangement involving chromosomes 2, 4, and 6 detected by fluorescence in situ hybridization (FISH).
Hoffman DJ; Punnett HH; Pyeritz RE
Am J Perinatol; 2004 Feb; 21(2):69-71. PubMed ID: 15017469
[TBL] [Abstract][Full Text] [Related]
11. Newborn with malformations and a combined duplication of 9pter-q22 and 16q22-qter resulting from unbalanced segregation of a complex maternal translocation.
Piram A; Ortolan D; Peres LC; Pina-Neto JM; Riegel M; Schinzel A
Am J Med Genet A; 2003 Jul; 120A(2):247-52. PubMed ID: 12833408
[TBL] [Abstract][Full Text] [Related]
12. Wolf-Hirschorn syndrome resulting from partial monosomy 4p/trisomy 9p.
Xu J; Freeman V; Carter RF; Paes B; Heshka T; Nowaczyk JM
Am J Med Genet; 2000 Aug; 93(4):285-9. PubMed ID: 10946354
[TBL] [Abstract][Full Text] [Related]
13. Partial trisomy of the distal part of 10q: a report of two Egyptian cases.
Aglan MS; Kamel AK; Helmy NA
Genet Couns; 2008; 19(2):199-209. PubMed ID: 18618995
[TBL] [Abstract][Full Text] [Related]
14. Duplication 5q and deletion 9p due to a t(5;9)(q34;p23) in 2 cousins with features of Hunter-McAlpine syndrome and hypothyroidism.
Vásquez-Velásquez AI; García-Castillo HA; González-Mercado MG; Dávalos IP; Raca G; Xu X; Dwyer E; Rivera H
Cytogenet Genome Res; 2011; 132(4):233-8. PubMed ID: 21063078
[TBL] [Abstract][Full Text] [Related]
15. Additional chromosome in a child as a result of a balanced reciprocal translocation t(12;18)(p13;q12) in his mother's karyotype.
Lassota M; Przełozna B; Płodzien M; Bugno M; Wnuk M; Kotylak Z; Słota E
J Appl Genet; 2005; 46(4):419-21. PubMed ID: 16278518
[TBL] [Abstract][Full Text] [Related]
16. Partial trisomy 1p due to paternal t(1;9) translocation in a family with recurrent miscarriages.
Demirhan O; Tastemir D
Fertil Steril; 2006 Jul; 86(1):219.e15-9. PubMed ID: 16818035
[TBL] [Abstract][Full Text] [Related]
17. Clinical and genomic characterization of siblings with a distal duplication of chromosome 9q (9q34.1-qter).
Mizuno S; Fukushi D; Kimura R; Yamada K; Yamada Y; Kumagai T; Wakamatsu N
Am J Med Genet A; 2011 Sep; 155A(9):2274-80. PubMed ID: 21834029
[TBL] [Abstract][Full Text] [Related]
18. Duplication 9q34-->qter identified by chromosome painting.
Spinner NB; Lucas JN; Poggensee M; Jacquette M; Schneider A
Am J Med Genet; 1993 Mar; 45(5):609-13. PubMed ID: 8456834
[TBL] [Abstract][Full Text] [Related]
19. Partial monosomy 8q and partial trisomy 9q due to the maternal translocation t(8;9(q24.3;q34.1): a case report.
Tos T; Alp MY; Eker HK; Cebi AH; Ikbal M
Genet Couns; 2014; 25(1):35-9. PubMed ID: 24783653
[TBL] [Abstract][Full Text] [Related]
20. Delineation of a supernumerary marker chromosome utilizing a multimodal approach of G-banding, fluorescent in situ hybridization, confirmatory P1 artificial chromosome fluorescent in situ hybridization, and high-resolution comparative genomic hybridization.
Mark HF; Wyandt H; Huang XL; Milunsky JM
Clin Genet; 2005 Aug; 68(2):146-51. PubMed ID: 15996211
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]