Chromosomal microarray analysis as the first-tier test for the identification of pathogenic copy number variants in chromosome 9 pericentric regions and its challenge

por Wang, Jia-Chi, Boyar, Fatih Z.
Publicado 2016

Isochromosome Yp and jumping translocation of Yq resulting in five cell lines in an infertile male: a case report and review of the literature

por Hemmat, Morteza, Hemmat, Omid, Boyar, Fatih Z
Publicado 2013

Enrichment of small pathogenic deletions at chromosome 9p24.3 and 9q34.3 involving DOCK8, KANK1, EHMT1 genes identified by using high-resolution oligonucleotide-single nucleotide p...

por Wang, Jia-Chi, Mahon, Loretta W., Ross, Leslie P., Anguiano, Arturo, Owen, Renius, Boyar, Fatih Z.
Publicado 2016

Neocentric X-chromosome in a girl with Turner-like syndrome

por Hemmat, Morteza, Wang, Boris T, Warburton, Peter E, Yang, Xiaojing, Boyar, Fatih Z, El Naggar, Mohammed, Anguiano, Arturo
Publicado 2012

Short stature, digit anomalies and dysmorphic facial features are associated with the duplication of miR-17 ~ 92 cluster

por Hemmat, Morteza, Rumple, Melissa J, Mahon, Loretta W, Strom, Charles M, Anguiano, Arturo, Talai, Maryam, Nguyen, Bryant, Boyar, Fatih Z
Publicado 2014

CMA analysis identifies homozygous deletion of MCPH1 in 2 brothers with primary Microcephaly-1

por Hemmat, Morteza, Rumple, Melissa J, Mahon, Loretta W, Morrow, Melanie, Zach, Tamara, Anguiano, Arturo, Elnaggar, Mohamed M, Wang, Boris T, Boyar, Fatih Z
Publicado 2017

Genotype-phenotype analysis of recombinant chromosome 4 syndrome: an array-CGH study and literature review

por Hemmat, Morteza, Hemmat, Omid, Anguiano, Arturo, Boyar, Fatih Z, El Naggar, Mohammed, Wang, Jia-Chi, Wang, Borris T, Sahoo, Trilochan, Owen, Renius, Haddadin, Mary
Publicado 2013

Submicroscopic deletion of 5q involving tumor suppressor genes (CTNNA1, HSPA9) and copy neutral loss of heterozygosity associated with TET2 and EZH2 mutations in a case of MDS with...

por Hemmat, Morteza, Chen, Weina, Anguiano, Arturo, Naggar, Mohammed El, Racke, Frederick K, Jones, Dan, Wang, Yongbao, Strom, Charles M, Chang, Karl, Boyar, Fatih Z
Publicado 2014

Identification and clinical evaluation of segments of homozygosity, uniparental disomy and complex chromosomal abnormalities revealed by copy-number SNP arrays

por Wang, Jia-Chi, Ross, Leslie, Mahon, Loretta W, Owen, Renius, Hemmat, Morteza, Wang, Boris T, El Naggar, Mohammed, Kopita, Kimberly A, Haddadin, Mary, Boyar, Fatih Z, Anguiano, Arturo, Strom, Charles M, Sahoo, Trilochan
Publicado 2014

Abnormalities in spontaneous abortions detected by G-banding and chromosomal microarray analysis (CMA) at a national reference laboratory

por Wang, Boris T, Chong, Thomas P, Boyar, Fatih Z, Kopita, Kimberly A, Ross, Leslie P, El-Naggar, Mohamed M, Sahoo, Trilochan, Wang, Jia-Chi, Hemmat, Morteza, Haddadin, Mary H, Owen, Renius, Anguiano, Arturo L
Publicado 2014

Characterization of a complex chromosomal rearrangement using chromosome, FISH, and microarray assays in a girl with multiple congenital abnormalities and developmental delay

por Hemmat, Morteza, Yang, Xiaojing, Chan, Patricia, McGough, Robert A, Ross, Leslie, Mahon, Loretta W, Anguiano, Arturo L, Boris, Wang T, Elnaggar, Mohamed M, Wang, Jia-Chi J, Strom, Charles M, Boyar, Fatih Z
Publicado 2014

Spectral Karyotyping for identification of constitutional chromosomal abnormalities at a national reference laboratory

por Anguiano, Arturo, Wang, Boris T, Wang, Shirong R, Boyar, Fatih Z, Mahon, Loretta W, El Naggar, Mohamed M, Kohn, Peter H, Haddadin, Mary H, Sulcova, Vladimira, Sbeiti, Adam H, Ayad, Mervat S, White, Beverly J, Strom, Charles M
Publicado 2012