Literature DB >> 12362042

Pure terminal duplication of the short arm of chromosome 19 in a boy with mild microcephaly.

S Andries, D Sartenaer, K Rack, S Rombout, D Tuerlinckx, Y Gillerot, L Van Maldergem.   

Abstract

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Year:  2002        PMID： 12362042      PMCID： PMC1734980          DOI： 10.1136/jmg.39.10.e60

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  3 in total

1.  Duplication of 19p13.3 in 11-Year-Old Male Patient with Dysmorphic Features and Intellectual Disability: A Review.

Authors:  Irina Novikova; Paushpala Sen; Ann Manzardo; Merlin G Butler
Journal:  J Pediatr Genet       Date:  2017-06-02

2.  Limited survivability of unbalanced progeny of carriers of a unique t(4;19)(p15.32;p13.3): a study in multiple generations.

Authors:  Darinka Šumanović-Glamuzina; Bernarda Lozić; Piotr S Iwanowski; Tatijana Zemunik; Zeljka Bilinovac; Beata Stasiewicz-Jarocka; Barbara Panasiuk; Alina T Midro
Journal:  Mol Cytogenet       Date:  2017-08-04       Impact factor: 2.009

3.  A novel immunodeficiency syndrome associated with partial trisomy 19p13.

Authors:  Markus G Seidel; Celia Duerr; Stavroula Woutsas; Anette Schwerin-Nagel; Kambis Sadeghi; Jürgen Neesen; Sabine Uhrig; Elisangela Santos-Valente; Winfried F Pickl; Wolfgang Schwinger; Christian Urban; Kaan Boztug; Elisabeth Förster-Waldl
Journal:  J Med Genet       Date:  2014-01-15       Impact factor: 6.318
  3 in total

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