Publications by authors named "Kemal O Yariz"

7Publications

Novel domain-specific POU3F4 mutations are associated with X-linked deafness: examples from different populations.

BMC Med Genet 2015 Feb 25;16. Epub 2015 Feb 25.

John P. Hussmann Institute for Human Genomics and John T. Macdonald Foundation, Department of Human Genetics, Miller school of Medicine, University of Miami, 1501 NW 10th Avenue, BRB-610 (M-860), Miami, FL, 33136, USA.

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February 2015

An amino acid deletion inSZT2 in a family with non-syndromic intellectual disability.

PLoS One 2013 6;8(12):e82810. Epub 2013 Dec 6.

Dr. John T. Macdonald Department of Human Genetics and John P. Hussman Institute for Human Genomics, Miller School of Medicine, University of Miami, Miami, Florida, United States of America.

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July 2014

Inherited mutation of the luteinizing hormone/choriogonadotropin receptor (LHCGR) in empty follicle syndrome.

Fertil Steril 2011 Aug 17;96(2):e125-30. Epub 2011 Jun 17.

Department of Human Genetics and Institute for Human Genomics, University of Miami School of Medicine, Miami, Florida, USA.

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August 2011