581 related articles for article (PubMed ID: 20420036)
1. 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]
2. 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]
3. Trisomy for the short arm of chromosome 10. Report of a new case resulting from segregation of a maternal balanced translocation t(10qter----q11::14p11----qter).
Delaroche I; Bruni L; Giannotti A; Giampaolo R; Aebischer ML
Helv Paediatr Acta; 1984 May; 39(2):161-6. PubMed ID: 6543839
[TBL] [Abstract][Full Text] [Related]
4. [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]
5. [Marker chromosomes as a product of familial translocation (11;22) identified with molecular cytogenetic methods].
Stankiewicz P; Korniszewski L; Bocian E; Stańczak H
Pediatr Pol; 1996 Mar; 71(3):241-5. PubMed ID: 8966096
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. [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]
8. 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]
9. Familial trisomy 20p five cases and two carriers in three generations a review.
Centerwall W; Francke U
Ann Genet; 1977 Jun; 20(2):77-83. PubMed ID: 302689
[TBL] [Abstract][Full Text] [Related]
10. Supernumerary chromosome marker Der(22)t(11;22) resulting from a maternal balanced translocation.
Hou JW
Chang Gung Med J; 2003 Jan; 26(1):48-52. PubMed ID: 12656309
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 8q22-->qter duplication in a child with multiple congenital malformations: case report.
Sasiadek M; Stembalska A; Schlade K; Zych M
Med Sci Monit; 2000; 6(1):141-4. PubMed ID: 11208302
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Identification of a subtle chromosomal translocation in a family with recurrent miscarriages and a child with multiple congenital anomalies. A case report.
Shaffer LG; Spikes AS; Macha M; Dunn R
J Reprod Med; 1996 May; 41(5):367-71. PubMed ID: 8725766
[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. Identification of an unbalanced cryptic translocation between the chromosomes 8 and 13 in two sisters with mild mental retardation accompanied by mild dysmorphic features.
Kleefstra T; van de Zande G; Merkx G; Mieloo H; Hoovers JM; Smeets D
Eur J Hum Genet; 2000 Aug; 8(8):637-40. PubMed ID: 10951526
[TBL] [Abstract][Full Text] [Related]
17. Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype.
Lin CC; Hsieh YY; Wang CH; Li YC; Hsieh LJ; Lee CC; Tsai CH; Tsai FJ
Prenat Diagn; 2006 Oct; 26(10):898-902. PubMed ID: 16915592
[TBL] [Abstract][Full Text] [Related]
18. Trisomy 9p syndrome in two brothers: with new clinical findings and review of the literature.
Hacihanefioğlu S; Güven GS; Deviren A; Silahtaroğlu AN; Yosunvkaya Fenerci E; Ozkiliç A; Yüksel A
Genet Couns; 2002; 13(1):41-8. PubMed ID: 12017237
[TBL] [Abstract][Full Text] [Related]
19. Meiotic segregation in familial reciprocal translocation t(8q;22q).
Gödde-Salz E; Oesinghaus S; Grote W
Am J Med Genet; 1982 Feb; 11(2):241-7. PubMed ID: 7065009
[TBL] [Abstract][Full Text] [Related]
20. Molecular analysis of a complex chromosomal rearrangement and a review of familial cases.
Batista DA; Pai GS; Stetten G
Am J Med Genet; 1994 Nov; 53(3):255-63. PubMed ID: 7856662
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]