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Journal of Translational Medicine
|
June 10, 2023
Implementation of Nanopore sequencing as a pragmatic workflow for copy number variant confirmation in the clinic
Stephanie U Greer, Jacquelin Botello, Donna Hongo, et al.
American Journal of Medical Genetics. Part A
|
November 23, 2011
Duplication of the ZIC2 gene is not associated with holoprosencephaly
Vaidehi Jobanputra, Alanna Burke, Anyane-Yeboa Kwame, et al.
Fertility and Sterility
|
April 4, 2013
In vitro fertilization with single euploid blastocyst transfer: a randomized controlled trial
Eric J Forman, Kathleen H Hong, Kathleen M Ferry, et al.
Hormone Research in Paediatrics
|
June 16, 2017
Prevalence and Physical Distribution of SRY in the Gonads of a Woman with Turner Syndrome: Phenotypic Presentation, Tubal Formation, and Malignancy Risk
Tamar G Baer, Christopher E Freeman, Claudia Cujar, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 18, 2007
Microarray analysis for constitutional cytogenetic abnormalities
Lisa G Shaffer, Arthur L Beaudet, Arthur R Brothman, et al.
Frontiers in Genetics
|
August 5, 2022
Case Report: Prenatal Identification of a <i>De Novo</i> Mosaic Neocentric Marker Resulting in 13q31.1→qter Tetrasomy in a Mildly Affected Girl
Avinash V Dharmadhikari, Elaine M Pereira, Carli C Andrews, et al.
Matrix Biology : Journal of the International Society for Matrix Biology
|
December 8, 2004
Genomic organization and sequence variation of the human integrin subunit alpha8 gene (ITGA8)
Catherine Ekwa-Ekoka, George A Diaz, Chris Carlson, et al.
Journal of Dermatological Science
|
August 11, 2010
Ambras syndrome in a Korean patient with balanced pericentric inversion (8)(p11.2q24.2)
Juwon Kim, Goeun Lee, Jong Rak Choi, et al.
Obstetrics and Gynecology
|
July 9, 2014
Genomic imbalance in products of conception: single-nucleotide polymorphism chromosomal microarray analysis
Brynn Levy, Styrmir Sigurjonsson, Barbara Pettersen, et al.
Prenatal Diagnosis
|
October 31, 2012
Noninvasive prenatal aneuploidy testing of chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic loci
Bernhard Zimmermann, Matthew Hill, George Gemelos, et al.
Page
of 13
Search research articles
Search
Showing results (61-70 of 122) with videos related to
Sort By:
Page
of 13
Journal of Translational Medicine
|
June 10, 2023
Implementation of Nanopore sequencing as a pragmatic workflow for copy number variant confirmation in the clinic
Stephanie U Greer, Jacquelin Botello, Donna Hongo, et al.
American Journal of Medical Genetics. Part A
|
November 23, 2011
Duplication of the ZIC2 gene is not associated with holoprosencephaly
Vaidehi Jobanputra, Alanna Burke, Anyane-Yeboa Kwame, et al.
Fertility and Sterility
|
April 4, 2013
In vitro fertilization with single euploid blastocyst transfer: a randomized controlled trial
Eric J Forman, Kathleen H Hong, Kathleen M Ferry, et al.
Hormone Research in Paediatrics
|
June 16, 2017
Prevalence and Physical Distribution of SRY in the Gonads of a Woman with Turner Syndrome: Phenotypic Presentation, Tubal Formation, and Malignancy Risk
Tamar G Baer, Christopher E Freeman, Claudia Cujar, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 18, 2007
Microarray analysis for constitutional cytogenetic abnormalities
Lisa G Shaffer, Arthur L Beaudet, Arthur R Brothman, et al.
Frontiers in Genetics
|
August 5, 2022
Case Report: Prenatal Identification of a <i>De Novo</i> Mosaic Neocentric Marker Resulting in 13q31.1→qter Tetrasomy in a Mildly Affected Girl
Avinash V Dharmadhikari, Elaine M Pereira, Carli C Andrews, et al.
Matrix Biology : Journal of the International Society for Matrix Biology
|
December 8, 2004
Genomic organization and sequence variation of the human integrin subunit alpha8 gene (ITGA8)
Catherine Ekwa-Ekoka, George A Diaz, Chris Carlson, et al.
Journal of Dermatological Science
|
August 11, 2010
Ambras syndrome in a Korean patient with balanced pericentric inversion (8)(p11.2q24.2)
Juwon Kim, Goeun Lee, Jong Rak Choi, et al.
Obstetrics and Gynecology
|
July 9, 2014
Genomic imbalance in products of conception: single-nucleotide polymorphism chromosomal microarray analysis
Brynn Levy, Styrmir Sigurjonsson, Barbara Pettersen, et al.
Prenatal Diagnosis
|
October 31, 2012
Noninvasive prenatal aneuploidy testing of chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic loci
Bernhard Zimmermann, Matthew Hill, George Gemelos, et al.
Page
of 13