Publications by authors named "Gayle S Patel"

3Publications

Dosage changes of a segment at 17p13.1 lead to intellectual disability and microcephaly as a result of complex genetic interaction of multiple genes.

Authors:
Claudia M B Carvalho Shivakumar Vasanth Marwan Shinawi Chad Russell Melissa B Ramocki Chester W Brown Jesper Graakjaer Anne-Bine Skytte Angela M Vianna-Morgante Ana C V Krepischi Gayle S Patel LaDonna Immken Kyrieckos Aleck Cynthia Lim Sau Wai Cheung Carla Rosenberg Nicholas Katsanis James R Lupski

Am J Hum Genet 2014 Nov 6;95(5):565-78. Epub 2014 Nov 6.

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA; Department of Pediatrics, Baylor College of Medicine, Houston, TX 77030, USA; Texas Children's Hospital, Houston, TX 77030, USA. Electronic address:

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November 2014

Deletions in chromosome 6p22.3-p24.3, including ATXN1, are associated with developmental delay and autism spectrum disorders.

Authors:
Patrícia Bs Celestino-Soper Cindy Skinner Richard Schroer Patricia Eng Jayant Shenai Malgorzata Mj Nowaczyk Deborah Terespolsky Donna Cushing Gayle S Patel Ladonna Immken Alecia Willis Joanna Wiszniewska Reuben Matalon Jill A Rosenfeld Roger E Stevenson Sung-Hae L Kang Sau Wai Cheung Arthur L Beaudet Pawel Stankiewicz

Mol Cytogenet 2012 Apr 5;5:17. Epub 2012 Apr 5.

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.

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April 2012

Int22h-1/int22h-2-mediated Xq28 rearrangements: intellectual disability associated with duplications and in utero male lethality with deletions.

Authors:
Ayman W El-Hattab Ping Fang Weihong Jin Jeffrey R Hughes James B Gibson Gayle S Patel Dorothy K Grange Linda P Manwaring Ankita Patel Pawel Stankiewicz Sau Wai Cheung

J Med Genet 2011 Dec 8;48(12):840-50. Epub 2011 Oct 8.

Division of Medical Genetics, Department of Child Health, University of Missouri Health Care, Columbia, Missouri, USA.

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December 2011