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 em 2013

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 em 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 em 2014

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 em 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 em 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 em 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 em 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 no Mol Cytogenet (2014)

Regions of homozygosity identified by oligonucleotide SNP arrays: evaluating the incidence and clinical utility

Por Wang, Jia-Chi, Ross, Leslie, Mahon, Loretta W, Owen, Renius, Hemmat, Morteza, Wang, Boris T, El Naggar, Mohammed, Kopita, Kimberly A, Randolph, Linda M, Chase, John M, Matas Aguilera, Maria J, Siles, Juan López, Church, Joseph A, Hauser, Natalie, Shen, Joseph J, Jones, Marilyn C, Wierenga, Klaas J, Jiang, Zhijie, Haddadin, Mary, Boyar, Fatih Z, Anguiano, Arturo, Strom, Charles M, Sahoo, Trilochan
Publicado no Eur J Hum Genet (2015)