396 related articles for article (PubMed ID: 21644216)
1. [Two cases of partial trisomy 8p derived from paternal reciprocal translocation or maternal insertion translocation: clinical features and genetic abnormalities].
Xiao B; Zhang JM; Ji X; Jiang WT; Hu J; Tao J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Jun; 28(3):247-50. PubMed ID: 21644216
[TBL] [Abstract][Full Text] [Related]
2. [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]
3. [Paternally originated Wolf-Hirschhorn syndrome detected by multiplex ligation-dependent probe amplification and microarray comparative genomic hybridization].
Zhu CJ; Huang ZY; Wu WQ; Zhao Q; Jiang HY; Xie JS
Zhonghua Er Ke Za Zhi; 2012 Jun; 50(6):460-4. PubMed ID: 22931946
[TBL] [Abstract][Full Text] [Related]
4. [Prenatal diagnosis of a fetus with partial trisomy 8p resulting from a balanced maternal translocation by array-based comparative genomic hybridization].
Guo C; Wang J; Zhao L; Liu J; Wang J; Xiao J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Jun; 32(3):375-7. PubMed ID: 26037354
[TBL] [Abstract][Full Text] [Related]
5. [Cytogenetic and molecular characterization of partial trisomy 4q and partial monosomy 10q in a patient].
Zhang YL; Dai Y; Tu ZG; Li QY; Wang LQ; Zhang L; Zeng J; Ouyang ZB
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Apr; 27(2):153-7. PubMed ID: 20376795
[TBL] [Abstract][Full Text] [Related]
6. Partial monosomy 13q (13q21.32--->qter) and partial trisomy 8p (8p1--->pter) presenting with anencephaly and increased nuchal translucency: array comparative genomic hybridization characterization.
Chen CP; Su YN; Tsai FJ; Lin MH; Wu PC; Chern SR; Lee CC; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2011 Jun; 50(2):205-11. PubMed ID: 21791309
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Clinical and cytogenetic features of a patient with partial trisomy 8q and partial monosomy 13q delineated by array comparative genomic hybridization.
Sohn YB; Yun JN; Park SJ; Park MS; Kim SH; Lee JH
Ann Clin Lab Sci; 2013; 43(3):332-6. PubMed ID: 23884231
[TBL] [Abstract][Full Text] [Related]
9. Proximal trisomy 13q and distal monosomy 8p in a dysmorphic and mentally retarded patient with an isodicentric chromosome 13q and a 13q/8p translocation chromosome.
Lukusa T; van den Berghe L; Smeets E; Fryns JP
Ann Genet; 1999; 42(4):215-20. PubMed ID: 10674161
[TBL] [Abstract][Full Text] [Related]
10. A cryptic duplication 22q13.31 to qter leads to a distinct phenotype with mental retardation, microcephaly and mild facial dysmorphism.
Peeters H; Vermeesch J; Fryns JP
Genet Couns; 2008; 19(4):365-71. PubMed ID: 19239079
[TBL] [Abstract][Full Text] [Related]
11. Maternal balanced translocation (4;21) leading to an offspring with partial duplication of 4q and 21q without phenotypic manifestations of Down syndrome.
El-Ruby M; Hemly NA; Zaki MS
Genet Couns; 2007; 18(2):217-26. PubMed ID: 17710874
[TBL] [Abstract][Full Text] [Related]
12. Phenotype and micro-array characterization of duplication 11q22.1-q25 and review of the literature.
Ben-Abdallah-Bouhjar I; Mougou-Zerelli S; Hannachi H; Ben-Khelifa H; Soyah N; Labalme A; Sanlaville D; Elghezal H; Saad A
Gene; 2013 Apr; 519(1):135-41. PubMed ID: 23403231
[TBL] [Abstract][Full Text] [Related]
13. Segregation of a paternal insertional translocation results in partial 4q monosomy or 4q trisomy in two siblings.
Hegmann KM; Spikes AS; Orr-Urtreger A; Shaffer LG
Am J Med Genet; 1996 Jan; 61(1):10-5. PubMed ID: 8741910
[TBL] [Abstract][Full Text] [Related]
14. Prenatal diagnosis of partial monosomy 8p (8p23.2→pter) and partial trisomy 15q (15q21.2→qter) and incidental detection of a familial chromosome translocation of paternal origin in a pregnancy associated with increased nuchal translucency and an abnormal maternal serum screening result.
Chen CP; Ko TM; Wang LK; Chern SR; Wu PS; Chen SW; Wu FT; Chen LF; Wang W
Taiwan J Obstet Gynecol; 2021 Jul; 60(4):775-777. PubMed ID: 34247824
[TBL] [Abstract][Full Text] [Related]
15. Trisomy of chromosome 16p13.3 due to an unbalanced insertional translocation into chromosome 22p13.
de Ravel T; Aerssens P; Vermeesch JR; Fryns JP
Eur J Med Genet; 2005; 48(3):355-9. PubMed ID: 16179232
[TBL] [Abstract][Full Text] [Related]
16. Distal 2q duplication: report of two familial cases and an attempt to define a syndrome.
Zankl M; Schwanitz G; Schmid P; Zankl H; Dockter G; Rodewald A; Zang KD; Grosse KP
Am J Med Genet; 1979; 4(1):5-16. PubMed ID: 495653
[TBL] [Abstract][Full Text] [Related]
17. Partial trisomy 8p (8p11.2-->pTER) and deletion of 13q (13q32-->qTER): case report.
Yeşilyurt A; Dilli D; Oguz S; Dilmen U; Altug N; Candemir Z
Genet Couns; 2011; 22(1):35-40. PubMed ID: 21614986
[TBL] [Abstract][Full Text] [Related]
18. Array-CGH and clinical findings in a patient with a small supernumerary r(8) mosaicism.
Eyüpoğlu FC; Sünnetçi D; Cine N; Savli H; Okten A; Açikgöz EG; Sönmez FM
Genet Couns; 2014; 25(3):305-13. PubMed ID: 25365853
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Double partial trisomy of 6p23-pter and 9pter-q21.2 in a neonate resulting from 4:2 meiotic segregation of a maternal complex t(6;7;9)(p23;p15;q21.2) translocation.
Cetin Z; Mihci E; Keser I; Karaali K; Berker S; Luleci G
Genet Couns; 2012; 23(2):239-47. PubMed ID: 22876583
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]