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Scott D McLean

Showing results (11-20 of 25) with videos related to

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Journal of Pediatric Urology|December 7, 2020
Patterns of co-occurring birth defects among infants with hypospadiasKatherine L Ludorf, Renata H Benjamin, Maria Luisa Navarro Sanchez, et al.
Journal of Pediatric Urology|July 30, 2021
Corrigendum to "Patterns of co-occurring birth defects among infants with hypospadiasˮ [J Pediatr Urol 17 (2021) 64.e1-64.e8]Katherine L Ludorf, Renata H Benjamin, Maria Luisa Navarro Sanchez, et al.
Ophthalmic Epidemiology|December 21, 2020
A Comprehensive Assessment of Co-occurring Birth Defects among Infants with Non-Syndromic Anophthalmia or MicrophthalmiaJeremy M Schraw, Renata H Benjamin, Daryl A Scott, et al.
American Journal of Medical Genetics. Part A|March 22, 2021
Patterns of congenital anomalies among individuals with trisomy 13 in TexasDiego Diaz, Renata H Benjamin, Maria Luisa Navarro Sanchez, et al.
American Journal of Medical Genetics. Part A|September 5, 2020
Birth defects that co-occur with non-syndromic gastroschisis and omphaloceleOmobola O Oluwafemi, Renata H Benjamin, Maria Luisa Navarro Sanchez, et al.
American Journal of Human Genetics|August 23, 2016
De Novo Truncating Variants in SON Cause Intellectual Disability, Congenital Malformations, and Failure to ThriveMari J Tokita, Alicia A Braxton, Yunru Shao, et al.
Cell|September 20, 2011
Chromosome catastrophes involve replication mechanisms generating complex genomic rearrangementsPengfei Liu, Ayelet Erez, Sandesh C Sreenath Nagamani, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 26, 2024
DISP1 deficiency: Monoallelic and biallelic variants cause a spectrum of midline craniofacial malformationsAlinoë Lavillaureix, Paul Rollier, Artem Kim, et al.
Neurology|July 2, 2017
<i>DNM1</i> encephalopathy: A new disease of vesicle fissionSarah von Spiczak, Katherine L Helbig, Deepali N Shinde, et al.
The Journal of Clinical Endocrinology and Metabolism|January 12, 2023
Intranasal Carbetocin Reduces Hyperphagia, Anxiousness, and Distress in Prader-Willi Syndrome: CARE-PWS Phase 3 TrialElizabeth Roof, Cheri L Deal, Shawn E McCandless, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Journal of Pediatric Urology|December 7, 2020
Patterns of co-occurring birth defects among infants with hypospadiasKatherine L Ludorf, Renata H Benjamin, Maria Luisa Navarro Sanchez, et al.
Journal of Pediatric Urology|July 30, 2021
Corrigendum to "Patterns of co-occurring birth defects among infants with hypospadiasˮ [J Pediatr Urol 17 (2021) 64.e1-64.e8]Katherine L Ludorf, Renata H Benjamin, Maria Luisa Navarro Sanchez, et al.
Ophthalmic Epidemiology|December 21, 2020
A Comprehensive Assessment of Co-occurring Birth Defects among Infants with Non-Syndromic Anophthalmia or MicrophthalmiaJeremy M Schraw, Renata H Benjamin, Daryl A Scott, et al.
American Journal of Medical Genetics. Part A|March 22, 2021
Patterns of congenital anomalies among individuals with trisomy 13 in TexasDiego Diaz, Renata H Benjamin, Maria Luisa Navarro Sanchez, et al.
American Journal of Medical Genetics. Part A|September 5, 2020
Birth defects that co-occur with non-syndromic gastroschisis and omphaloceleOmobola O Oluwafemi, Renata H Benjamin, Maria Luisa Navarro Sanchez, et al.
American Journal of Human Genetics|August 23, 2016
De Novo Truncating Variants in SON Cause Intellectual Disability, Congenital Malformations, and Failure to ThriveMari J Tokita, Alicia A Braxton, Yunru Shao, et al.
Cell|September 20, 2011
Chromosome catastrophes involve replication mechanisms generating complex genomic rearrangementsPengfei Liu, Ayelet Erez, Sandesh C Sreenath Nagamani, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 26, 2024
DISP1 deficiency: Monoallelic and biallelic variants cause a spectrum of midline craniofacial malformationsAlinoë Lavillaureix, Paul Rollier, Artem Kim, et al.
Neurology|July 2, 2017
<i>DNM1</i> encephalopathy: A new disease of vesicle fissionSarah von Spiczak, Katherine L Helbig, Deepali N Shinde, et al.
The Journal of Clinical Endocrinology and Metabolism|January 12, 2023
Intranasal Carbetocin Reduces Hyperphagia, Anxiousness, and Distress in Prader-Willi Syndrome: CARE-PWS Phase 3 TrialElizabeth Roof, Cheri L Deal, Shawn E McCandless, et al.
Pageof 3