129 related articles for article (PubMed ID: 21344639)
1. Molecular cytogenetic and clinical characterization of a patient with a 5.6-Mb deletion in 7p15 including HOXA cluster.
Jun KR; Seo EJ; Lee JO; Yoo HW; Park IS; Yoon HK
Am J Med Genet A; 2011 Mar; 155A(3):642-7. PubMed ID: 21344639
[TBL] [Abstract][Full Text] [Related]
2. Familial deletion of the HOXA gene cluster associated with Hand-Foot-Genital syndrome and phenotypic variability.
Tas E; Sebastian J; Madan-Khetarpal S; Sweet P; Yatsenko AN; Pollock N; Rajkovic A; Schneck FX; Yatsenko SA; Witchel SF
Am J Med Genet A; 2017 Jan; 173(1):221-224. PubMed ID: 27649277
[TBL] [Abstract][Full Text] [Related]
3. HOXA genes cluster: clinical implications of the smallest deletion.
Pezzani L; Milani D; Manzoni F; Baccarin M; Silipigni R; Guerneri S; Esposito S
Ital J Pediatr; 2015 Apr; 41():31. PubMed ID: 25881986
[TBL] [Abstract][Full Text] [Related]
4. Deletion involving the TWIST locus and the HOXA cluster: a contiguous gene syndrome on 7p?
Kosaki R; Higuchi M; Mitsui N; Matsushima K; Ohashi H; Kosaki K
Congenit Anom (Kyoto); 2005 Mar; 45(1):35-8. PubMed ID: 15737130
[TBL] [Abstract][Full Text] [Related]
5. Facial dysgenesis: a novel facial syndrome with chromosome 7 deletion p15.1-21.1.
Hoover-Fong JE; Cai J; Cargile CB; Thomas GH; Patel A; Griffin CA; Jabs EW; Hamosh A
Am J Med Genet A; 2003 Feb; 117A(1):47-56. PubMed ID: 12548740
[TBL] [Abstract][Full Text] [Related]
6. [Phenotypic and genetic characteristics of a child with 7p15 deletion syndrome].
Wu J; Dou B; Meng G; Wang H; Hou Y; Xia J; Bai Y; Kong X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Aug; 37(8):855-858. PubMed ID: 32761594
[TBL] [Abstract][Full Text] [Related]
7. Absence of skeletal anomalies in siblings with a maternally inherited 12q13.13-q13.2 microdeletion partially involving the HOXC gene cluster.
Peterson JF; Hartman J; Ghaloul-Gonzalez L; Surti U; Hu J
Am J Med Genet A; 2014 Mar; 164A(3):810-4. PubMed ID: 24443387
[TBL] [Abstract][Full Text] [Related]
8. Molecular cytogenetic characterization of a constitutional, highly complex intrachromosomal rearrangement of chromosome 1, with 14 breakpoints and a 0.5 Mb submicroscopic deletion.
Lindstrand A; Malmgren H; Sahlén S; Xin H; Schoumans J; Blennow E
Am J Med Genet A; 2008 Dec; 146A(24):3217-22. PubMed ID: 19006217
[No Abstract] [Full Text] [Related]
9. A 13-year-old boy with a 7q36.1q36.3 deletion with additional findings.
Hyohyeon C; Lee CG
Am J Med Genet A; 2015 Jan; 167A(1):198-203. PubMed ID: 25257745
[TBL] [Abstract][Full Text] [Related]
10. Submicroscopic deletion of 12q13 including HOXC gene cluster with skeletal anomalies and global developmental delay.
Okamoto N; Tamura D; Nishimura G; Shimojima K; Yamamoto T
Am J Med Genet A; 2011 Dec; 155A(12):2997-3001. PubMed ID: 22069146
[TBL] [Abstract][Full Text] [Related]
11. Cytogenetic and molecular characterization of a de-novo cryptic deletion of 7p21 associated with an apparently balanced translocation and complex craniosynostosis.
Shetty S; Boycott KM; Gillan TL; Bowser K; Parboosingh JS; McInnes B; Chernos JE; Bernier FP
Clin Dysmorphol; 2007 Oct; 16(4):253-6. PubMed ID: 17786117
[TBL] [Abstract][Full Text] [Related]
12. A novel 2.43 Mb deletion of 7q11.22-q11.23.
Blyth M; Beal S; Huang S; Crolla J; Foulds N
Am J Med Genet A; 2008 Dec; 146A(24):3206-10. PubMed ID: 19012340
[TBL] [Abstract][Full Text] [Related]
13. 2q24 deletions: further characterization of clinical findings and their relation to the SCN cluster.
Nimmakayalu M; Noble N; Horton VK; Willing M; Copeland S; Sheffield V; Nagy PL; Wassink T; Patil S; Shchelochkov OA
Am J Med Genet A; 2012 Nov; 158A(11):2767-74. PubMed ID: 23023937
[TBL] [Abstract][Full Text] [Related]
14. The chromosome translocation t(7;11)(p15;p15) in acute myeloid leukemia results in fusion of the NUP98 gene with a HOXA cluster gene, HOXA13, but not HOXA9.
Taketani T; Taki T; Ono R; Kobayashi Y; Ida K; Hayashi Y
Genes Chromosomes Cancer; 2002 Aug; 34(4):437-43. PubMed ID: 12112533
[TBL] [Abstract][Full Text] [Related]
15. Cytogenomic and phenotypic analysis in low-level monosomy 7 mosaicism with non-supernumerary ring chromosome 7.
Salas-Labadía C; Cervantes-Barragán DE; Cruz-Alcívar R; Daber RD; Conlin LK; Leonard LD; Spinner NB; Durán-McKinster C; Dávila-Ortíz de Montellano DJ; Del Castillo-Ruiz V; Pérez-Vera P
Am J Med Genet A; 2014 Jul; 164A(7):1765-9. PubMed ID: 24677512
[TBL] [Abstract][Full Text] [Related]
16. Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects.
Kuo YL; Chen CP; Wang LK; Ko TM; Chang TY; Chern SR; Wu PS; Chen YT; Chang SY
Taiwan J Obstet Gynecol; 2014 Jun; 53(2):248-51. PubMed ID: 25017279
[TBL] [Abstract][Full Text] [Related]
17. Haploinsufficiency and triploinsensitivity of the same 6p25.1p24.3 region in a family.
Qi Z; Jeng LJ; Slavotinek A; Yu J
BMC Med Genomics; 2015 Jul; 8():38. PubMed ID: 26174853
[TBL] [Abstract][Full Text] [Related]
18. Rare genomic rearrangement in a boy with Williams-Beuren syndrome associated to XYY syndrome and intriguing behavior.
Dutra RL; Piazzon FB; Zanardo ÉA; Costa TV; Montenegro MM; Novo-Filho GM; Dias AT; Nascimento AM; Kim CA; Kulikowski LD
Am J Med Genet A; 2015 Dec; 167A(12):3197-203. PubMed ID: 26420477
[TBL] [Abstract][Full Text] [Related]
19. Molecular characterization of a patient with 3p deletion syndrome and a review of the literature.
Fernandez TV; García-González IJ; Mason CE; Hernández-Zaragoza G; Ledezma-Rodríguez VC; Anguiano-Alvarez VM; E'Vega R; Gutiérrez-Angulo M; Maya ML; García-Bejarano HE; González-Cruz M; Barrios S; Atorga R; López-Cardona MG; Armendariz-Borunda J; State MW; Dávalos NO
Am J Med Genet A; 2008 Nov; 146A(21):2746-52. PubMed ID: 18837054
[TBL] [Abstract][Full Text] [Related]
20. A patient with five chromosomal rearrangements and a 2q31.1 microdeletion.
Wang T; Mao J; Liu MJ; Choy KW; Li HB; Cram DS; Li H; Chen Y
Clin Chim Acta; 2014 Mar; 430():129-33. PubMed ID: 24412318
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]