Literature DB >> 11173835

Microdeletion 4p16.3 in three unrelated patients with Wolf-Hirschhorn syndrome.

A Dufke1, J Seidel, M Schöning, M Döbler-Neumann, C Kelbova, T Liehr, V Beensen, C Backsch, U Klein-Vogler, H Enders.   

Abstract

Wolf-Hirschhorn syndrome (WHS) is a multiple malformation syndrome caused by partial monosomy of 4p16.3. Pitt-Rogers-Danks syndrome, first thought to be a distinct entity, is a similar condition associated with a microdeletion overlapping the WHS critical region. In this paper we evaluate three WHS patients showing a microdeletion of 4p and remarkable development with respect to the clinical spectrum of WHS. Copyright 2001 S. Karger AG, Basel

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Year:  2000        PMID: 11173835     DOI: 10.1159/000056823

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN: 0301-0171


  2 in total

1.  Smash++: an alignment-free and memory-efficient tool to find genomic rearrangements.

Authors:  Morteza Hosseini; Diogo Pratas; Burkhard Morgenstern; Armando J Pinho
Journal:  Gigascience       Date:  2020-05-01       Impact factor: 6.524

Review 2.  A multiple translocation event in a patient with hexadactyly, facial dysmorphism, mental retardation and behaviour disorder characterised comprehensively by molecular cytogenetics. Case report and review of the literature.

Authors:  Jörg Seidel; Anita Heller; Gabriele Senger; Heike Starke; Ilse Chudoba; Christina Kelbova; Holger Tönnies; Heidemarie Neitzel; Claudia Haase; Volkmar Beensen; Felix Zintl; Uwe Claussen; Thomas Liehr
Journal:  Eur J Pediatr       Date:  2003-06-19       Impact factor: 3.183

  2 in total

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