Literature DB >> 10530074

Terminal deletion of chromosome 10q: clinical features and literature review.

S Tanabe1, T Akiba, M Katoh, T Satoh.   

Abstract

Mesh：

Year:  1999        PMID： 10530074     DOI： 10.1046/j.1442-200x.1999.01105.x

Source DB:  PubMed          Journal:  Pediatr Int        ISSN： 1328-8067            Impact factor:   1.524


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  4 in total

1.  Molecular (SNP) analyses of overlapping hemizygous deletions of 10q25.3 to 10qter in four patients: evidence for HMX2 and HMX3 as candidate genes in hearing and vestibular function.

Authors:  Nathaniel D Miller; Melonie A Nance; Elizabeth S Wohler; Julie E Hoover-Fong; Emily Lisi; George H Thomas; Jonathan Pevsner
Journal:  Am J Med Genet A       Date:  2009-02-15       Impact factor: 2.802

2.  Monosomy 10q26-qter and trisomy 11q13-qter as a result of de novo unbalanced translocation.

Authors:  F Tinsa; Y Chebbi; M Meddeb; D Bousnina; K Boussetta; S Bousnina
Journal:  J Appl Genet       Date:  2009       Impact factor: 3.240

3.  An unbalanced translocation involving loss of 10q26.2 and gain of 11q25 in a pedigree with autism spectrum disorder and cerebellar juvenile pilocytic astrocytoma.

Authors:  Hassan M Minhas; Matthew F Pescosolido; Matthew Schwede; Justyna Piasecka; John Gaitanis; Umadevi Tantravahi; Eric M Morrow
Journal:  Am J Med Genet A       Date:  2013-03-12       Impact factor: 2.802

Review 4.  A Case of Inherited t(4;10)(q26;q26.2) Chromosomal Translocation Elucidated by Multiple Chromosomal and Molecular Analyses. Case Report and Review of the Literature.

Authors:  Roxana Popescu; Mihaela Grămescu; Lavinia Caba; Monica-Cristina Pânzaru; Lăcrămioara Butnariu; Elena Braha; Setalia Popa; Cristina Rusu; Georgeta Cardos; Monica Zeleniuc; Violeta Martiniuc; Cristina Gug; Luminiţa Păduraru; Maria Stamatin; Carmen C Diaconu; Eusebiu Vlad Gorduza
Journal:  Genes (Basel)       Date:  2021-12-07       Impact factor: 4.096
  4 in total

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