Literature DB >> 7224998

The ascertainment and implications of an unbalanced translocation in the neonate. Familial 1:15 translocation.

D Hain, M Leversha, N Campbell, A Daniel, P A Barr, J G Rogers.   

Abstract

Mesh：

Year:  1980        PMID： 7224998     DOI： 10.1111/j.1440-1754.1980.tb01296.x

Source DB:  PubMed          Journal:  Aust Paediatr J        ISSN： 0004-993X


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  7 in total

1.  Chromosome 1p36 deletions: the clinical phenotype and molecular characterization of a common newly delineated syndrome.

Authors:  S K Shapira; C McCaskill; H Northrup; A S Spikes; F F Elder; V R Sutton; J R Korenberg; F Greenberg; L G Shaffer
Journal:  Am J Hum Genet       Date:  1997-09       Impact factor: 11.025

2.  Clinical consequences of deletion 1p35.

Authors:  S L Wenger; M W Steele; D J Becker
Journal:  J Med Genet       Date:  1988-04       Impact factor: 6.318

Review 3.  Monosomy 1p36.

Authors:  A Slavotinek; L G Shaffer; S K Shapira
Journal:  J Med Genet       Date:  1999-09       Impact factor: 6.318

4.  An azoospermic male with reciprocal translocation t(1;15) (q11;p11).

Authors:  C López-Ginés; R Gil; M Gregori-Romero; A Pellin
Journal:  Hum Genet       Date:  1987-11       Impact factor: 4.132

5.  Interstitial deletion 1p in a 30 year old woman.

Authors:  M B Petersen; M Warburg
Journal:  J Med Genet       Date:  1987-04       Impact factor: 6.318

6.  Outcome of Vertical Expandable Prosthetic Titanium Rib (VEPTR) Instrumentation in Scoliosis Associated With 1p36 Deletion Syndrome: A Case Report.

Authors:  Ozair Bin Majid; Mohammed A Al Rushud; Zayed Al-Zayed; Ghadeer Alsager; Jehangir A Bhat
Journal:  Cureus       Date:  2022-01-23

Review 7.  1p36 deletion syndrome: an update.

Authors:  Valerie K Jordan; Hitisha P Zaveri; Daryl A Scott
Journal:  Appl Clin Genet       Date:  2015-08-27
  7 in total

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