Wednesday, November 7, 2012

Genetics in Medicine contents: Volume 14, Issue 11


TABLE OF CONTENTS

Volume 14, Issue 11 (November 2012)

In this issue
Research Highlights
Original Research Article
ACMG College News

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Research Highlights

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In This Issue

Genet Med 2012 14: 889; 10.1038/gim.2012.137

Full Text

News Briefs

Genet Med 2012 14: 889-890; 10.1038/gim.2012.146

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Original Research Articles

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Next-generation sequencing in health-care delivery: lessons from the functional analysis of rhodopsin

Wayne I.L. Davies, Susan M. Downes, Josephine K. Fu, Morag E. Shanks, Richard R. Copley, Stefano Lise, Simon C. Ramsden, Graeme C. M. Black, Kate Gibson, Russell G. Foster, Mark W. Hankins and Andrea H. Németh

Genet Med 2012 14: 891-899; advance online publication, July 12, 2012; 10.1038/gim.2012.73

Abstract | Full Text

Homozygous null mutation in ODZ3 causes microphthalmia in humans

Mohammed A. Aldahmesh, Jawahir Y. Mohammed, Selwa Al-Hazzaa and Fowzan S. Alkuraya

Genet Med 2012 14: 900-904; advance online publication, July 5, 2012; 10.1038/gim.2012.71

Abstract | Full Text

Women’s and health professionals’ preferences for prenatal tests for Down syndrome: a discrete choice experiment to contrast noninvasive prenatal diagnosis with current invasive tests

Melissa Hill, Jane Fisher, Lyn S. Chitty and Stephen Morris

Genet Med 2012 14: 905-913; advance online publication, August 30, 2012; 10.1038/gim.2012.68

Abstract | Full Text

Defining the impact of maternal cell contamination on the interpretation of prenatal microarray analysis

Allen N. Lamb, Jill A. Rosenfeld, Justine Coppinger, Erin T. Dodge, Mindy Preston Dabell, Beth S. Torchia, J. Britt Ravnan, Lisa G. Shaffer and Blake C. Ballif

Genet Med 2012 14: 914-921; advance online publication, July 5, 2012; 10.1038/gim.2012.77

Abstract | Full Text

The pulmonary artery in patients with Marfan syndrome: a cross-sectional study

Rigmor Lundby, Svend Rand-Hendriksen, John K. Hald, Are Hugo Pripp and Hans-Jørgen Smith

Genet Med 2012 14: 922-927; advance online publication, July 12, 2012; 10.1038/gim.2012.82

Abstract | Full Text

Novel candidate genes and regions for childhood apraxia of speech identified by array comparative genomic hybridization

Jennifer J.S. Laffin, Gordana Raca, Craig A. Jackson, Edythe A. Strand, Kathy J. Jakielski and Lawrence D. Shriberg

Genet Med 2012 14: 928-936; advance online publication, July 5, 2012; 10.1038/gim.2012.72

Abstract | Full Text

Birth prevalence of disorders detectable through newborn screening by race/ethnicity

Lisa Feuchtbaum, Jennifer Carter, Sunaina Dowray, Robert J. Currier and Fred Lorey

Genet Med 2012 14: 937-945; advance online publication, July 5, 2012; 10.1038/gim.2012.76

Abstract | Full Text

ACMG College News

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ACMG College news

Genet Med 2012 14: 946-947; 10.1038/gim.2012.140

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