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Molecular Genetics & Genomic Medicine
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September 4, 2019
Inverted duplication, triplication and quintuplication through sequential breakage-fusion-bridge events induced by a terminal deletion at 5p in a case of spontaneous abortion
Hongyan Chai, Brittany Grommisch, Autumn DiAdamo, et al.
American Journal of Medical Genetics. Part A
|
July 16, 2008
Analytical and clinical validity of whole-genome oligonucleotide array comparative genomic hybridization for pediatric patients with mental retardation and developmental delay
Bixia Xiang, Ao Li, Dinu Valentin, et al.
Human Pathology
|
July 29, 2008
Congenital fibrosarcoma with a novel complex 3-way translocation t(12;15;19) and unusual histologic features
Adrián Mariño-Enríquez, Peining Li, Joan Samuelson, et al.
Human Pathology
|
July 19, 2014
Recurrent chromosomal aberrations in intravenous leiomyomatosis of the uterus: high-resolution array comparative genomic hybridization study
Natalia Buza, Fang Xu, Weiqing Wu, et al.
Case Reports in Genetics
|
December 21, 2020
Cytogenomic Abnormalities in 19 Cases of Salivary Gland Tumors of Parotid Gland Origin
Marie Zerjav, Autumn DiAdamo, Brittany Grommisch, et al.
Leukemia & Lymphoma
|
April 29, 2016
Recurrent genetic defects in classical Hodgkin lymphoma cell lines
S David Hudnall, Hailong Meng, Larissa Lozovatsky, et al.
HGG Advances
|
October 3, 2022
The past, present, and future for constitutional ring chromosomes: A report of the international consortium for human ring chromosomes
Peining Li, Barbara Dupont, Qiping Hu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
May 11, 2021
[Experience and lessons on guiding and governing clinical applications of chromosome microarray analysis in the United States]
Xiaolei Xie, Jingwei Yu, Zhongxia Qi, et al.
Global Medical Genetics
|
June 16, 2022
Genotype-Phenotype Correlations for Putative Haploinsufficient Genes in Deletions of 6q26-q27: Report of Eight Patients and Review of Literature
Xiaolei Xie, Hongyan Chai, Autumn DiAdamo, et al.
Molecular Cytogenetics
|
December 24, 2015
Copy number changes and methylation patterns in an isodicentric and a ring chromosome of 15q11-q13: report of two cases and review of literature
Qin Wang, Weiqing Wu, Zhiyong Xu, et al.
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Search research articles
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Showing results (31-40 of 130) with videos related to
Sort By:
Page
of 13
Molecular Genetics & Genomic Medicine
|
September 4, 2019
Inverted duplication, triplication and quintuplication through sequential breakage-fusion-bridge events induced by a terminal deletion at 5p in a case of spontaneous abortion
Hongyan Chai, Brittany Grommisch, Autumn DiAdamo, et al.
American Journal of Medical Genetics. Part A
|
July 16, 2008
Analytical and clinical validity of whole-genome oligonucleotide array comparative genomic hybridization for pediatric patients with mental retardation and developmental delay
Bixia Xiang, Ao Li, Dinu Valentin, et al.
Human Pathology
|
July 29, 2008
Congenital fibrosarcoma with a novel complex 3-way translocation t(12;15;19) and unusual histologic features
Adrián Mariño-Enríquez, Peining Li, Joan Samuelson, et al.
Human Pathology
|
July 19, 2014
Recurrent chromosomal aberrations in intravenous leiomyomatosis of the uterus: high-resolution array comparative genomic hybridization study
Natalia Buza, Fang Xu, Weiqing Wu, et al.
Case Reports in Genetics
|
December 21, 2020
Cytogenomic Abnormalities in 19 Cases of Salivary Gland Tumors of Parotid Gland Origin
Marie Zerjav, Autumn DiAdamo, Brittany Grommisch, et al.
Leukemia & Lymphoma
|
April 29, 2016
Recurrent genetic defects in classical Hodgkin lymphoma cell lines
S David Hudnall, Hailong Meng, Larissa Lozovatsky, et al.
HGG Advances
|
October 3, 2022
The past, present, and future for constitutional ring chromosomes: A report of the international consortium for human ring chromosomes
Peining Li, Barbara Dupont, Qiping Hu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
May 11, 2021
[Experience and lessons on guiding and governing clinical applications of chromosome microarray analysis in the United States]
Xiaolei Xie, Jingwei Yu, Zhongxia Qi, et al.
Global Medical Genetics
|
June 16, 2022
Genotype-Phenotype Correlations for Putative Haploinsufficient Genes in Deletions of 6q26-q27: Report of Eight Patients and Review of Literature
Xiaolei Xie, Hongyan Chai, Autumn DiAdamo, et al.
Molecular Cytogenetics
|
December 24, 2015
Copy number changes and methylation patterns in an isodicentric and a ring chromosome of 15q11-q13: report of two cases and review of literature
Qin Wang, Weiqing Wu, Zhiyong Xu, et al.
Page
of 13