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Showing results (991-1000 of 998) with videos related to

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Nature Genetics|January 10, 2017
SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndromeNatalie D Shaw, Harrison Brand, Zachary A Kupchinsky, et al.
Genetics in Medicine Open|September 30, 2024
Regulatory elements in <i>SEM1-DLX5-DLX6</i> (7q21.3) locus contribute to genetic control of coronal nonsyndromic craniosynostosis and bone density-related traitsPaola Nicoletti, Samreen Zafer, Lital Matok, et al.
Brain : a Journal of Neurology|December 14, 2019
MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsisChristopher C Y Mak, Dan Doherty, Angela E Lin, et al.
JAMA Network Open|June 10, 2024
Severe Pediatric Neurological Manifestations With SARS-CoV-2 or MIS-C Hospitalization and New MorbidityConall Francoeur, Alicia M Alcamo, Courtney L Robertson, et al.
Cell|June 20, 2015
Ebola Virus Epidemiology, Transmission, and Evolution during Seven Months in Sierra LeoneDaniel J Park, Gytis Dudas, Shirlee Wohl, et al.
Biological Psychiatry|August 25, 2019
Partial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor β SignalingBrett V Johnson, Raman Kumar, Sabrina Oishi, et al.
Nature|October 15, 2020
Inherited causes of clonal haematopoiesis in 97,691 whole genomesAlexander G Bick, Joshua S Weinstock, Satish K Nandakumar, et al.
Nature|March 12, 2021
Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomesAlexander G Bick, Joshua S Weinstock, Satish K Nandakumar, et al.
Pageof 100

Showing results (991-1000 of 998) with videos related to

Sort By:
Pageof 100
You have reached the last page of results.This site can display upto 998 results.
Nature Genetics|January 10, 2017
SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndromeNatalie D Shaw, Harrison Brand, Zachary A Kupchinsky, et al.
Genetics in Medicine Open|September 30, 2024
Regulatory elements in <i>SEM1-DLX5-DLX6</i> (7q21.3) locus contribute to genetic control of coronal nonsyndromic craniosynostosis and bone density-related traitsPaola Nicoletti, Samreen Zafer, Lital Matok, et al.
Brain : a Journal of Neurology|December 14, 2019
MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsisChristopher C Y Mak, Dan Doherty, Angela E Lin, et al.
JAMA Network Open|June 10, 2024
Severe Pediatric Neurological Manifestations With SARS-CoV-2 or MIS-C Hospitalization and New MorbidityConall Francoeur, Alicia M Alcamo, Courtney L Robertson, et al.
Cell|June 20, 2015
Ebola Virus Epidemiology, Transmission, and Evolution during Seven Months in Sierra LeoneDaniel J Park, Gytis Dudas, Shirlee Wohl, et al.
Biological Psychiatry|August 25, 2019
Partial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor β SignalingBrett V Johnson, Raman Kumar, Sabrina Oishi, et al.
Nature|October 15, 2020
Inherited causes of clonal haematopoiesis in 97,691 whole genomesAlexander G Bick, Joshua S Weinstock, Satish K Nandakumar, et al.
Nature|March 12, 2021
Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomesAlexander G Bick, Joshua S Weinstock, Satish K Nandakumar, et al.
Pageof 100