Literature DB >> 6609675

Occurrence of 19p- in an infant with multiple dysmorphic features.

V Hurgoiu, S Suciu.   

Abstract

A case with partial deletion on the short arm of one chromosome 19 and multiple dysmorphic features is reported.

Entities:  

Mesh：

Year:  1984        PMID： 6609675

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


  5 in total

Review 1.  Telomeres: a diagnosis at the end of the chromosomes.

Authors:  B B A De Vries; R Winter; A Schinzel; C van Ravenswaaij-Arts
Journal:  J Med Genet       Date:  2003-06       Impact factor: 6.318

2.  A novel chromosome 19p13.12 deletion in a child with multiple congenital anomalies.

Authors:  Daniel R Jensen; Donna M Martin; Stephen Gebarski; Trilochan Sahoo; Ellen K Brundage; A Craig Chinault; Edgar A Otto; Moumita Chaki; Friedhelm Hildebrandt; Sau Wai Cheung; Marci M Lesperance
Journal:  Am J Med Genet A       Date:  2009-03       Impact factor: 2.802

3.  Chromosome 19p13.3 deletion in a child with Peutz-Jeghers syndrome, congenital heart defect, high myopia, learning difficulties and dysmorphic features: Clinical and molecular characterization of a new contiguous gene syndrome.

Authors:  Josiane Souza; Fábio Faucz; Vanessa Sotomaior; Aguinaldo Bonalumi Filho; Jill Rosenfeld; Salmo Raskin
Journal:  Genet Mol Biol       Date:  2011-10-01       Impact factor: 1.771

4.  Ocular Manifestations of a Novel Proximal 19p13.3 Microdeletion.

Authors:  L Swan; D Coman
Journal:  Case Rep Genet       Date:  2018-04-30

5.  Perinatal findings in a patient with a novel large chromosome 19p deletion.

Authors:  Marko Culjat; Jennifer Razak; Reem Saadeh-Haddad; Rita Driggers; Karen Kamholz; Julia Timofeev
Journal:  Clin Case Rep       Date:  2018-06-21
  5 in total

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