Literature DB >> 6979302

Interstitial deletion of the long arm of chromosome 15.

J P Fryns, A de Muelenaere, H van den Berghe.   

Abstract

Mesh：

Year:  1982        PMID： 6979302

Source DB:  PubMed          Journal:  Ann Genet        ISSN： 0003-3995


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  9 in total

1.  Deletion 15q21.1----q22.1 resulting from a paternal insertion into chromosome 5.

Authors:  M Y Yip; M Selikowitz; N Don; A Kovacic; S Purvis-Smith; P R Lam-Po-Tang
Journal:  J Med Genet       Date:  1987-11       Impact factor: 6.318

2.  Interstitial deletion of chromosome 15: two cases.

Authors:  L D Formiga; L Poenaru; F Couronne; E Flori; J L Eibel; M M Deminatti; J B Savary; J L Lai; S Gilgenkrantz; M Pierson
Journal:  Hum Genet       Date:  1988-12       Impact factor: 4.132

3.  A de novo interstitial deletion of 15(q21.2q22.1) in a moderately retarded adult male.

Authors:  F Martin; J Platt; E J Tawn; J Burn
Journal:  J Med Genet       Date:  1990-10       Impact factor: 6.318

4.  The clinical spectrum of complete FBN1 allele deletions.

Authors:  Yvonne Hilhorst-Hofstee; Ben C J Hamel; Joke B G M Verheij; Marry E B Rijlaarsdam; Grazia M S Mancini; Jan M Cobben; Cindy Giroth; Claudia A L Ruivenkamp; Kerstin B M Hansson; Janneke Timmermans; Henriette A Moll; Martijn H Breuning; Gerard Pals
Journal:  Eur J Hum Genet       Date:  2010-11-10       Impact factor: 4.246

Review 5.  Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysis.

Authors:  M G Mattei; N Souiah; J F Mattei
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

6.  An infant with deletion of the distal long arm of chromosome 15 (q26.1----qter) and loss of insulin-like growth factor 1 receptor gene.

Authors:  E W Roback; A J Barakat; V G Dev; M Mbikay; M Chrétien; M G Butler
Journal:  Am J Med Genet       Date:  1991-01

7.  Coarctation of the aorta and mild to moderate developmental delay in a child with a de novo deletion of chromosome 15(q21.1q22.2).

Authors:  Seema R Lalani; Trilochan Sahoo; Merideth E Sanders; Sarika U Peters; Bassem A Bejjani
Journal:  BMC Med Genet       Date:  2006-02-10       Impact factor: 2.103

8.  Mapping Breakpoints of Complex Chromosome Rearrangements Involving a Partial Trisomy 15q23.1-q26.2 Revealed by Next Generation Sequencing and Conventional Techniques.

Authors:  Qiong Pan; Hao Hu; Liangrong Han; Xin Jing; Hailiang Liu; Chuanchun Yang; Fengting Zhang; Yue Hu; Hongni Yue; Ying Ning
Journal:  PLoS One       Date:  2016-05-24       Impact factor: 3.240

9.  Response to Growth Hormone Treatment in a Patient with Insulin-Like Growth Factor 1 Receptor Deletion.

Authors:  Ranim Mahmoud; Ajanta Naidu; Hiba Risheg; Virginia Kimonis
Journal:  J Clin Res Pediatr Endocrinol       Date:  2017-07-17
  9 in total

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