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Leigh Simpson

Showing results (71-80 of 135) with videos related to

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Fertility and Sterility|April 10, 2007
Mutation analysis of NANOS3 in 80 Chinese and 88 Caucasian women with premature ovarian failureYingying Qin, Han Zhao, Ertug Kovanci, et al.
Fertility and Sterility|May 8, 2007
Analyses of GDF9 mutation in 100 Chinese women with premature ovarian failureHan Zhao, Yingying Qin, Ertug Kovanci, et al.
Obstetrics and Gynecology Clinics of North America|April 18, 2003
Genetics of endometriosisJoe Leigh Simpson, Farideh Z Bischoff, Aparna Kamat, et al.
American Journal of Human Genetics|August 19, 2007
NOBOX homeobox mutation causes premature ovarian failureYingying Qin, Youngsok Choi, Han Zhao, et al.
Plos One|July 23, 2014
FMR1 premutation is an uncommon explanation for premature ovarian failure in Han ChineseTing Guo, Yingying Qin, Xue Jiao, et al.
Plos One|March 11, 2015
Spatial positioning of all 24 chromosomes in the lymphocytes of six subjects: evidence of reproducible positioning and spatial repositioning following DNA damage with hydrogen peroxide and ultraviolet BDimitrios Ioannou, Lakshmi Kandukuri, Ameer Quadri, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 3, 2006
Quantity versus quality: optimal methods for cell-free DNA isolation from plasma of pregnant womenCarolina J Jorgez, Dianne D Dang, Joe Leigh Simpson, et al.
Fertility and Sterility|October 22, 2008
Mutation analysis of NOBOX homeodomain in Chinese women with premature ovarian failureYingying Qin, Yuhua Shi, Yueran Zhao, et al.
International Journal of Gynaecology and Obstetrics: the Official Organ of the International Federation of Gynaecology and Obstetrics|September 14, 2021
FIGO good practice recommendations on progestogens for prevention of preterm deliveryAndrew Shennan, Natalie Suff, Joe Leigh Simpson, et al.
Neuro Endocrinology Letters|November 7, 2007
Novel non-synonymous mutation in the transforming growth factor beta binding protein-like (TB) domain of the fibrillin-1 (FBN1) gene in a Han Chinese family with Marfan syndrome (MFS)Yingying Qin, Junhao Yan, Joe Leigh Simpson, et al.
Pageof 14

Showing results (71-80 of 135) with videos related to

Sort By:
Pageof 14
Fertility and Sterility|April 10, 2007
Mutation analysis of NANOS3 in 80 Chinese and 88 Caucasian women with premature ovarian failureYingying Qin, Han Zhao, Ertug Kovanci, et al.
Fertility and Sterility|May 8, 2007
Analyses of GDF9 mutation in 100 Chinese women with premature ovarian failureHan Zhao, Yingying Qin, Ertug Kovanci, et al.
Obstetrics and Gynecology Clinics of North America|April 18, 2003
Genetics of endometriosisJoe Leigh Simpson, Farideh Z Bischoff, Aparna Kamat, et al.
American Journal of Human Genetics|August 19, 2007
NOBOX homeobox mutation causes premature ovarian failureYingying Qin, Youngsok Choi, Han Zhao, et al.
Plos One|July 23, 2014
FMR1 premutation is an uncommon explanation for premature ovarian failure in Han ChineseTing Guo, Yingying Qin, Xue Jiao, et al.
Plos One|March 11, 2015
Spatial positioning of all 24 chromosomes in the lymphocytes of six subjects: evidence of reproducible positioning and spatial repositioning following DNA damage with hydrogen peroxide and ultraviolet BDimitrios Ioannou, Lakshmi Kandukuri, Ameer Quadri, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 3, 2006
Quantity versus quality: optimal methods for cell-free DNA isolation from plasma of pregnant womenCarolina J Jorgez, Dianne D Dang, Joe Leigh Simpson, et al.
Fertility and Sterility|October 22, 2008
Mutation analysis of NOBOX homeodomain in Chinese women with premature ovarian failureYingying Qin, Yuhua Shi, Yueran Zhao, et al.
International Journal of Gynaecology and Obstetrics: the Official Organ of the International Federation of Gynaecology and Obstetrics|September 14, 2021
FIGO good practice recommendations on progestogens for prevention of preterm deliveryAndrew Shennan, Natalie Suff, Joe Leigh Simpson, et al.
Neuro Endocrinology Letters|November 7, 2007
Novel non-synonymous mutation in the transforming growth factor beta binding protein-like (TB) domain of the fibrillin-1 (FBN1) gene in a Han Chinese family with Marfan syndrome (MFS)Yingying Qin, Junhao Yan, Joe Leigh Simpson, et al.
Pageof 14