Molecular breakpoint cloning and gene expression studies of a novel translocation t(4;15)(q27;q11.2) associated with Prader-Willi syndrome

Journal article

Open access

Peer reviewed

Birgitt Schüle, Mohammed Albalwi, Emma Northrop, David I Francis, Margaret Rowell, Howard R Slater, RJ McKinlay Gardner and Uta Francke

BMC medical genetics, Vol.6(1), pp.18-18

06/05/2005

PMCID: PMC1142316

PMID: 15877813

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https://doi.org/10.1186/1471-2350-6-18View

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Title: Molecular breakpoint cloning and gene expression studies of a novel translocation t(4;15)(q27;q11.2) associated with Prader-Willi syndrome
Creators - without role: Birgitt Schüle - Stanford University
Mohammed Albalwi - Stanford University
Emma Northrop - Royal Children's Hospital
David I Francis - Stanford University School of Medicine
Margaret Rowell - Royal Children's Hospital
Howard R Slater - Royal Children's Hospital
RJ McKinlay Gardner - Royal Children's Hospital
Uta Francke - Stanford University
Publication Details: BMC medical genetics, Vol.6(1), pp.18-18
Publisher: BioMed Central
Identifiers: 9921863708331
Academic Unit: King Saud Bin Abdulaziz University for Health Sciences
Language: English
Resource Type: Journal article