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Chromosomal microarray vs. NIPS: analysis of 5541 low-risk pregnancies
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Chromosomal microarray vs. NIPS: analysis of 5541 low-risk pregnancies

Sagi-Dain, Lena ; Cohen Vig, Lital ; Kahana, Sarit ; Yacobson, Shiri ; Tenne, Tamar ; Agmon-Fishman, Ifat ; Klein, Cochava ; Matar, Reut ; Basel-Salmon, Lina ; Maya, Idit

Genetics in medicine, 2019-11, Vol.21 (11), p.2462-2467 [Periódico revisado por pares]

United States: Elsevier Limited

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2
Comprehensive genetic analysis of pregnancy loss by chromosomal microarrays: outcomes, benefits, and challenges
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Comprehensive genetic analysis of pregnancy loss by chromosomal microarrays: outcomes, benefits, and challenges

Sahoo, Trilochan ; Dzidic, Natasa ; Strecker, Michelle N. ; Commander, Sara ; Travis, Mary K. ; Doherty, Charles ; Tyson, R. Weslie ; Mendoza, Arturo E. ; Stephenson, Mary ; Dise, Craig A. ; Benito, Carlos W. ; Ziadie, Mandolin S. ; Hovanes, Karine

Genetics in medicine, 2017-01, Vol.19 (1), p.83-89 [Periódico revisado por pares]

United States: Elsevier Inc

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3
Low-pass whole-genome sequencing in clinical cytogenetics: a validated approach
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Low-pass whole-genome sequencing in clinical cytogenetics: a validated approach

Dong, Zirui ; Zhang, Jun ; Hu, Ping ; Chen, Haixiao ; Xu, Jinjin ; Tian, Qi ; Meng, Lu ; Ye, Yanchou ; Wang, Jun ; Zhang, Meiyan ; Li, Yun ; Wang, Huilin ; Yu, Shanshan ; Chen, Fang ; Xie, Jiansheng ; Jiang, Hui ; Wang, Wei ; Choy, Kwong Wai ; Xu, Zhengfeng

Genetics in medicine, 2016-09, Vol.18 (9), p.940-948 [Periódico revisado por pares]

United States: Elsevier Limited

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4
Comparison of chromosome analysis and chromosomal microarray analysis: what is the value of chromosome analysis in today’s genomic array era?
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Comparison of chromosome analysis and chromosomal microarray analysis: what is the value of chromosome analysis in today’s genomic array era?

Bi, Weimin ; Borgan, Caroline ; Pursley, Amber N. ; Hixson, Patricia ; Shaw, Chad A. ; Bacino, Carlos A. ; Lalani, Seema R. ; Patel, Ankita ; Stankiewicz, Pawel ; Lupski, James R. ; Beaudet, Arthur L. ; Cheung, Sau Wai

Genetics in medicine, 2013-06, Vol.15 (6), p.450-457 [Periódico revisado por pares]

United States: Elsevier Inc

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5
Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression
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Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression

Lowther, Chelsea ; Speevak, Marsha ; Armour, Christine M. ; Goh, Elaine S. ; Graham, Gail E. ; Li, Chumei ; Zeesman, Susan ; Nowaczyk, Malgorzata J.M. ; Schultz, Lee-Anne ; Morra, Antonella ; Nicolson, Rob ; Bikangaga, Peter ; Samdup, Dawa ; Zaazou, Mostafa ; Boyd, Kerry ; Jung, Jack H. ; Siu, Victoria ; Rajguru, Manjulata ; Goobie, Sharan ; Tarnopolsky, Mark A. ; Prasad, Chitra ; Dick, Paul T. ; Hussain, Asmaa S. ; Walinga, Margreet ; Reijenga, Renske G. ; Gazzellone, Matthew ; Lionel, Anath C. ; Marshall, Christian R. ; Scherer, Stephen W. ; Stavropoulos, Dimitri J. ; McCready, Elizabeth ; Bassett, Anne S.

Genetics in medicine, 2017-01, Vol.19 (1), p.53-61 [Periódico revisado por pares]

United States: Elsevier Inc

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6
Chromosomal microarray testing influences medical management
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Chromosomal microarray testing influences medical management

Coulter, Michael E ; Miller, David T ; Harris, David J ; Hawley, Pamela ; Picker, Jonathan ; Roberts, Amy E ; Sobeih, Magdi M ; Irons, Mira

Genetics in medicine, 2011-09, Vol.13 (9), p.770-776 [Periódico revisado por pares]

United States: Elsevier Limited

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7
A systematic analysis of small supernumerary marker chromosomes using array CGH exposes unexpected complexity
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A systematic analysis of small supernumerary marker chromosomes using array CGH exposes unexpected complexity

Reddy, Kavita S ; Aradhya, Swaroop ; Meck, Jeanne ; Tiller, George ; Abboy, Sridevi ; Bass, Harold

Genetics in medicine, 2013-01, Vol.15 (1), p.3-13 [Periódico revisado por pares]

United States: Elsevier Limited

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