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Arturo Anguiano

Showing results (1-10 of 16) with videos related to

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Pediatrics International : Official Journal of the Japan Pediatric Society|August 21, 2010
Paternal mosaic inv(20) resulting in a recombinant chromosome 20 in two siblingsBao-Tyan Wang, Morteza Hemmat, Parul Jayakar, et al.
Molecular Cytogenetics|November 29, 2016
Enrichment of small pathogenic deletions at chromosome 9p24.3 and 9q34.3 involving <i>DOCK8, KANK1, EHMT1</i> genes identified by using high-resolution oligonucleotide-single nucleotide polymorphism array analysisJia-Chi Wang, Loretta W Mahon, Leslie P Ross, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 17, 2006
A large deletion in the CFTR gene in CBAVDFeras M Hantash, Aubrey Milunsky, Zhenyuan Wang, et al.
Expert Opinion on Medical Diagnostics|March 19, 2013
Clinical array comparative genomic hybridization: a new paradigmPatricia Chan, Arturo Anguiano, Kerri Hensley, et al.
Molecular Cytogenetics|June 12, 2012
Neocentric X-chromosome in a girl with Turner-like syndromeMorteza Hemmat, Boris T Wang, Peter E Warburton, et al.
Molecular Cytogenetics|April 18, 2014
Short stature, digit anomalies and dysmorphic facial features are associated with the duplication of miR-17 ~ 92 clusterMorteza Hemmat, Melissa J Rumple, Loretta W Mahon, et al.
Journal of Pediatric Genetics|September 15, 2016
Inherited and de novo 22q11.2 distal duplications in two patients with autistic features, speech delay and no dysmorphologyFeras M Hantash, Boris T Wang, Renius Owen, et al.
Molecular Cytogenetics|September 8, 2017
CMA analysis identifies homozygous deletion of <i>MCPH1</i> in 2 brothers with primary Microcephaly-1Morteza Hemmat, Melissa J Rumple, Loretta W Mahon, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 17, 2006
CFTR 5T variant has a low penetrance in females that is partially attributable to its haplotypeWeimin Sun, Ben Anderson, Joy Redman, et al.
Molecular Cytogenetics|May 4, 2013
Genotype-phenotype analysis of recombinant chromosome 4 syndrome: an array-CGH study and literature reviewMorteza Hemmat, Omid Hemmat, Arturo Anguiano, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Pediatrics International : Official Journal of the Japan Pediatric Society|August 21, 2010
Paternal mosaic inv(20) resulting in a recombinant chromosome 20 in two siblingsBao-Tyan Wang, Morteza Hemmat, Parul Jayakar, et al.
Molecular Cytogenetics|November 29, 2016
Enrichment of small pathogenic deletions at chromosome 9p24.3 and 9q34.3 involving <i>DOCK8, KANK1, EHMT1</i> genes identified by using high-resolution oligonucleotide-single nucleotide polymorphism array analysisJia-Chi Wang, Loretta W Mahon, Leslie P Ross, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 17, 2006
A large deletion in the CFTR gene in CBAVDFeras M Hantash, Aubrey Milunsky, Zhenyuan Wang, et al.
Expert Opinion on Medical Diagnostics|March 19, 2013
Clinical array comparative genomic hybridization: a new paradigmPatricia Chan, Arturo Anguiano, Kerri Hensley, et al.
Molecular Cytogenetics|June 12, 2012
Neocentric X-chromosome in a girl with Turner-like syndromeMorteza Hemmat, Boris T Wang, Peter E Warburton, et al.
Molecular Cytogenetics|April 18, 2014
Short stature, digit anomalies and dysmorphic facial features are associated with the duplication of miR-17 ~ 92 clusterMorteza Hemmat, Melissa J Rumple, Loretta W Mahon, et al.
Journal of Pediatric Genetics|September 15, 2016
Inherited and de novo 22q11.2 distal duplications in two patients with autistic features, speech delay and no dysmorphologyFeras M Hantash, Boris T Wang, Renius Owen, et al.
Molecular Cytogenetics|September 8, 2017
CMA analysis identifies homozygous deletion of <i>MCPH1</i> in 2 brothers with primary Microcephaly-1Morteza Hemmat, Melissa J Rumple, Loretta W Mahon, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 17, 2006
CFTR 5T variant has a low penetrance in females that is partially attributable to its haplotypeWeimin Sun, Ben Anderson, Joy Redman, et al.
Molecular Cytogenetics|May 4, 2013
Genotype-phenotype analysis of recombinant chromosome 4 syndrome: an array-CGH study and literature reviewMorteza Hemmat, Omid Hemmat, Arturo Anguiano, et al.
Pageof 2