Literature DB >> 11746171

Prenatal diagnosis of mosaicism for deletion 22q13.3.

M C Phelan, E F Brown, R C Rogers.   

Abstract

Mesh：

Year:  2001        PMID： 11746171     DOI： 10.1002/pd.195

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN： 0197-3851            Impact factor:   3.050


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  3 in total

1.  Prenatal and postnatal diagnosis of Phelan-McDermid syndrome: A report of 21 cases from a medical center and review of the literature.

Authors:  Ying Hao; Yang Liu; Jingxin Yang; Xingping Li; Fuwei Luo; Qian Geng; Suli Li; Peining Li; Weiqing Wu; Jiansheng Xie
Journal:  Front Genet       Date:  2022-08-31       Impact factor: 4.772

2.  Mosaic 22q13 deletions: evidence for concurrent mosaic segmental isodisomy and gene conversion.

Authors:  Maria Clara Bonaglia; Roberto Giorda; Silvana Beri; Stefania Bigoni; Alberto Sensi; Anna Baroncini; Antonella Capucci; Cristina De Agostini; Rhian Gwilliam; Panos Deloukas; Ian Dunham; Orsetta Zuffardi
Journal:  Eur J Hum Genet       Date:  2008-10-15       Impact factor: 4.246

3.  Frequent chromosome aberrations revealed by molecular cytogenetic studies in patients with aniridia.

Authors:  John A Crolla; Veronica van Heyningen
Journal:  Am J Hum Genet       Date:  2002-10-17       Impact factor: 11.025
  3 in total

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