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Items: 2

1.
Characterization of the Chromosome 1q41q42.12 region, and the Candidate Gene DISP1, in Patients with CDH
Sibel Kantarci, Kate G Ackerman, Meaghan N Russell, Mauro Longoni, Carrie Sougnez, Kristin M Noonan, Eli Hatchwell, Xiaoyun Zhang, Rafael Pieretti Vanmarcke, Kwame Anyane-Yeboa, Paul Dickman, Jay Wilson, Patricia K Donahoe, Barbara R Pober
Am J Med Genet A. Author manuscript; available in PMC 2013 Oct 16.
Published in final edited form as: Am J Med Genet A. 2010 Oct; 0(10): 2493–2504. doi: 10.1002/ajmg.a.33618
PMCID:
PMC3797530
AbstractArticlePDF–1.3M
2.
Truncating loss-of-function mutations of DISP1 contribute to holoprosencephaly-like microform features in humans
Erich Roessler, Yong Ma, Maia V. Ouspenskaia, Felicitas Lacbawan, Claude Bendavid, Christèle Dubourg, Philip A. Beachy, Maximilian Muenke
Hum Genet. Author manuscript; available in PMC 2009 Nov 9.
Published in final edited form as: Hum Genet. 2009 May; 125(4): 393–400. Published online 2009 Jan 31. doi: 10.1007/s00439-009-0628-7
PMCID:
PMC2774849
AbstractArticlePDF–1.3M

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