Small rare recurrent deletions and reciprocal duplications in 2q21.1, including brain-specific ARHGEF4 and GPR148
Avinash V. Dharmadhikari(University of Southern California), Paweł Stankiewicz(Baylor College of Medicine), Melissa Williams, Sherry Vinson, John W. Belmont(Baylor College of Medicine), Vickie Hannig(Vanderbilt University Medical Center), Przemysław Szafrański(Baylor College of Medicine), Angus A. Wilfong(Baylor College of Medicine), Sau Wai Cheung(Chinese University of Hong Kong), Weimin Bi(Zhejiang A & F University), Ankita Patel(Gujarat University), Smita Sampath(Baylor College of Medicine), J.R. Lupski(Baylor College of Medicine), Shin-Sung Kang(Baylor College of Medicine), Patricia I. Bader(Counseling Center), W. J. Craigen(Baylor College of Medicine), Siddharth K. Prakash(The University of Texas Health Science Center at Houston), Richard Person(GenVec), Tyler Reimschisel(Vanderbilt University)
Cited by 36
Related Papers
A second generation human haplotype map of over 3.1 million SNPs
|Nature|2007|4.6k
Clinical Whole-Exome Sequencing for the Diagnosis of Mendelian Disorders
|New England Journal of Medicine|2013|2k
The 2017 international classification of the Ehlers–Danlos syndromes
|American Journal of Medical Genetics Part C Seminars in Medical Genetics|2017|1.9k
Chromosomal Microarray versus Karyotyping for Prenatal Diagnosis
|New England Journal of Medicine|2012|1.4k