Search research articles
Contact Us
Filters
Showing results (31-40 of 77) with videos related to
Page
of 8
Sort By:
BMC Urology
|
December 20, 2024
The initial clinical application of standard PCNL combined with visual needle nephroscope in the treatment of complex renal calculi by holmium YAG laser: a retrospective case series study
Engo Ovone Yanne, Bai Lin Wu, Cong Li, et al.
Journal of Cardiac Failure
|
March 9, 2010
Familial dilated cardiomyopathy secondary to dystrophin splice site mutation
Dita Obler, Bai-Lin Wu, Va Lip, et al.
Neuroscience Bulletin
|
June 5, 2021
GABA Signaling Pathway-associated Gene PLCL1 Rare Variants May be Associated with Autism Spectrum Disorders
Fengyun Zheng, Guoyuan Liu, Ting Dang, et al.
Archives of Otolaryngology--Head & Neck Surgery
|
January 20, 2010
Audiologic phenotype and progression in GJB2 (Connexin 26) hearing loss
Margaret A Kenna, Henry A Feldman, Marilyn W Neault, et al.
American Journal of Human Genetics
|
March 12, 2013
Molecular analysis of a deletion hotspot in the NRXN1 region reveals the involvement of short inverted repeats in deletion CNVs
Xiaoli Chen, Yiping Shen, Feng Zhang, et al.
Journal of Assisted Reproduction and Genetics
|
November 24, 2022
Majority of transferred mosaic embryos developed healthy live births revealed by a preclinical study using embryonic morphology assessment and noninvasive PGT-A on cell-free DNA in blastocoel fluid
Lingbo Cai, Qiao Zeng, Chao Gao, et al.
Archives of Neurology
|
August 13, 2008
Response of motor complications in Cockayne syndrome to carbidopa-levodopa
Edward G Neilan, Mauricio R Delgado, Melissa A Donovan, et al.
Journal of Developmental and Behavioral Pediatrics : JDBP
|
July 9, 2010
Cognitive and behavioral characterization of 16p11.2 deletion syndrome
Ellen Hanson, Ramzi H Nasir, Alexa Fong, et al.
Stem Cells and Development
|
April 29, 2015
Genetic Evaluation of Copy Number Variations, Loss of Heterozygosity, and Single-Nucleotide Variant Levels in Human Embryonic Stem Cells With or Without Skewed X Chromosome Inactivation
Wei-Qiang Liu, Jie-Liang Li, Jian Wang, et al.
Reproductive Biomedicine Online
|
June 11, 2014
Analysis of CGG repeats in FMR1 in Chinese women with idiopathic premature ovarian failure
Yuqin Ye, Xiaoping Lan, Jin Cong, et al.
Page
of 8
Search research articles
Search
Showing results (31-40 of 77) with videos related to
Sort By:
Page
of 8
BMC Urology
|
December 20, 2024
The initial clinical application of standard PCNL combined with visual needle nephroscope in the treatment of complex renal calculi by holmium YAG laser: a retrospective case series study
Engo Ovone Yanne, Bai Lin Wu, Cong Li, et al.
Journal of Cardiac Failure
|
March 9, 2010
Familial dilated cardiomyopathy secondary to dystrophin splice site mutation
Dita Obler, Bai-Lin Wu, Va Lip, et al.
Neuroscience Bulletin
|
June 5, 2021
GABA Signaling Pathway-associated Gene PLCL1 Rare Variants May be Associated with Autism Spectrum Disorders
Fengyun Zheng, Guoyuan Liu, Ting Dang, et al.
Archives of Otolaryngology--Head & Neck Surgery
|
January 20, 2010
Audiologic phenotype and progression in GJB2 (Connexin 26) hearing loss
Margaret A Kenna, Henry A Feldman, Marilyn W Neault, et al.
American Journal of Human Genetics
|
March 12, 2013
Molecular analysis of a deletion hotspot in the NRXN1 region reveals the involvement of short inverted repeats in deletion CNVs
Xiaoli Chen, Yiping Shen, Feng Zhang, et al.
Journal of Assisted Reproduction and Genetics
|
November 24, 2022
Majority of transferred mosaic embryos developed healthy live births revealed by a preclinical study using embryonic morphology assessment and noninvasive PGT-A on cell-free DNA in blastocoel fluid
Lingbo Cai, Qiao Zeng, Chao Gao, et al.
Archives of Neurology
|
August 13, 2008
Response of motor complications in Cockayne syndrome to carbidopa-levodopa
Edward G Neilan, Mauricio R Delgado, Melissa A Donovan, et al.
Journal of Developmental and Behavioral Pediatrics : JDBP
|
July 9, 2010
Cognitive and behavioral characterization of 16p11.2 deletion syndrome
Ellen Hanson, Ramzi H Nasir, Alexa Fong, et al.
Stem Cells and Development
|
April 29, 2015
Genetic Evaluation of Copy Number Variations, Loss of Heterozygosity, and Single-Nucleotide Variant Levels in Human Embryonic Stem Cells With or Without Skewed X Chromosome Inactivation
Wei-Qiang Liu, Jie-Liang Li, Jian Wang, et al.
Reproductive Biomedicine Online
|
June 11, 2014
Analysis of CGG repeats in FMR1 in Chinese women with idiopathic premature ovarian failure
Yuqin Ye, Xiaoping Lan, Jin Cong, et al.
Page
of 8