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Showing results (241-250 of 250) with videos related to

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Journal of Homosexuality|January 8, 2011
Suicide and suicide risk in lesbian, gay, bisexual, and transgender populations: review and recommendationsAnn P Haas, Mickey Eliason, Vickie M Mays, et al.
The European Respiratory Journal|July 30, 2016
High attenuation areas on chest computed tomography in community-dwelling adults: the MESA studyAnna J Podolanczuk, Elizabeth C Oelsner, R Graham Barr, et al.
Human Genetics|July 30, 2011
High-resolution array CGH defines critical regions and candidate genes for microcephaly, abnormalities of the corpus callosum, and seizure phenotypes in patients with microdeletions of 1q43q44Blake C Ballif, Jill A Rosenfeld, Ryan Traylor, et al.
American Journal of Human Genetics|April 19, 2023
POLR1A variants underlie phenotypic heterogeneity in craniofacial, neural, and cardiac anomaliesKelly Smallwood, Kristin E N Watt, Satoru Ide, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 18, 2022
Heterozygous variants in MYH10 associated with neurodevelopmental disorders and congenital anomalies with evidence for primary cilia-dependent defects in Hedgehog signalingAlexander M Holtz, Rachel VanCoillie, Elizabeth A Vansickle, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 20, 2021
Correction to: An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipidsSacha Ferdinandusse, Kirsty McWalter, Heleen Te Brinke, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 26, 2020
An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipidsSacha Ferdinandusse, Kirsty McWalter, Heleen Te Brinke, et al.
JAMA Network Open|October 12, 2023
Safety and Immunogenicity of Live Viral Vaccines in a Multicenter Cohort of Pediatric Transplant RecipientsAmy G Feldman, Brenda L Beaty, Jose A Ferrolino, et al.
JAMA Pediatrics|February 24, 2025
Postvaccination Immunogenicity Among Pediatric Solid Organ Transplant RecipientsAmy G Feldman, Brenda L Beaty, Jose A Ferrolino, et al.
American Journal of Human Genetics|July 10, 2026
Clinical, in vitro, and in vivo evidence of WAPL as a cohesinopathy-associated gene and phenotypic driver of 10q22.3q23.2 genomic disorderPhilip M Boone, Serkan Erdin, Abucar Mohamed, et al.
Pageof 25

Showing results (241-250 of 250) with videos related to

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Pageof 25
You have reached the last page of results.This site can display upto 250 results.
Journal of Homosexuality|January 8, 2011
Suicide and suicide risk in lesbian, gay, bisexual, and transgender populations: review and recommendationsAnn P Haas, Mickey Eliason, Vickie M Mays, et al.
The European Respiratory Journal|July 30, 2016
High attenuation areas on chest computed tomography in community-dwelling adults: the MESA studyAnna J Podolanczuk, Elizabeth C Oelsner, R Graham Barr, et al.
Human Genetics|July 30, 2011
High-resolution array CGH defines critical regions and candidate genes for microcephaly, abnormalities of the corpus callosum, and seizure phenotypes in patients with microdeletions of 1q43q44Blake C Ballif, Jill A Rosenfeld, Ryan Traylor, et al.
American Journal of Human Genetics|April 19, 2023
POLR1A variants underlie phenotypic heterogeneity in craniofacial, neural, and cardiac anomaliesKelly Smallwood, Kristin E N Watt, Satoru Ide, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 18, 2022
Heterozygous variants in MYH10 associated with neurodevelopmental disorders and congenital anomalies with evidence for primary cilia-dependent defects in Hedgehog signalingAlexander M Holtz, Rachel VanCoillie, Elizabeth A Vansickle, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 20, 2021
Correction to: An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipidsSacha Ferdinandusse, Kirsty McWalter, Heleen Te Brinke, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 26, 2020
An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipidsSacha Ferdinandusse, Kirsty McWalter, Heleen Te Brinke, et al.
JAMA Network Open|October 12, 2023
Safety and Immunogenicity of Live Viral Vaccines in a Multicenter Cohort of Pediatric Transplant RecipientsAmy G Feldman, Brenda L Beaty, Jose A Ferrolino, et al.
JAMA Pediatrics|February 24, 2025
Postvaccination Immunogenicity Among Pediatric Solid Organ Transplant RecipientsAmy G Feldman, Brenda L Beaty, Jose A Ferrolino, et al.
American Journal of Human Genetics|July 10, 2026
Clinical, in vitro, and in vivo evidence of WAPL as a cohesinopathy-associated gene and phenotypic driver of 10q22.3q23.2 genomic disorderPhilip M Boone, Serkan Erdin, Abucar Mohamed, et al.
Pageof 25