Fine Mapping of the 1p36 Deletion Syndrome Identifies Mutation of PRDM16 as a Cause of Cardiomyopathy-Reference-Cited by-同舟云学术

Fine Mapping of the 1p36 Deletion Syndrome Identifies Mutation of PRDM16 as a Cause of Cardiomyopathy

Published:2013-07 Issue:1 Volume:93 Page:67-77
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Arndt Anne-Karin,Schafer Sebastian,Drenckhahn Jorg-Detlef,Sabeh M. Khaled,Plovie Eva R.,Caliebe Almuth,Klopocki Eva,Musso Gabriel,Werdich Andreas A.,Kalwa Hermann,Heinig Matthias,Padera Robert F.,Wassilew Katharina,Bluhm Julia,Harnack Christine,Martitz Janine,Barton Paul J.,Greutmann Matthias,Berger Felix,Hubner Norbert,Siebert Reiner,Kramer Hans-Heiner,Cook Stuart A.,MacRae Calum A.,Klaassen Sabine

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference41 articles.

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3. Physical map of 1p36, placement of breakpoints in monosomy 1p36, and clinical characterization of the syndrome;Heilstedt;Am. J. Hum. Genet.,2003

4. Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation;Battaglia;Pediatrics,2008

5. Echocardiographic and pathoanatomical characteristics of isolated left ventricular non-compaction: a step towards classification as a distinct cardiomyopathy;Jenni;Heart,2001

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