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Lois J Starr

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American Journal of Medical Genetics. Part A|March 26, 2018
Newly described recessive MYH11 disorder with clinical overlap of Multisystemic smooth muscle dysfunction and Megacystis microcolon hypoperistalsis syndromesAnji T Yetman, Lois J Starr
World Journal for Pediatric & Congenital Heart Surgery|May 26, 2018
Kawasaki Disease in a Patient With Williams SyndromeAleisha M Nabower, Lois J Starr, Jonathan Cramer
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 1, 2024
The Myhre Syndrome Foundation as a global modern support group: The business of rareKate Wears, Angela E Lin, Lois J Starr
Journal for Specialists in Pediatric Nursing : JSPN|February 24, 2018
Autism spectrum disorder and genetic testing: Parental perceptions and decision-makingAlyson E Hanish, Marlene Z Cohen, Lois J Starr
Clinical Dysmorphology|March 24, 2021
Second reported individual with a partial STAG2 deletion: middle interhemispheric variant holoprosencephaly in STAG2-related cohesinopathyDrew M Cratsenberg, Peter J Winningham, Lois J Starr
Congenital Heart Disease|July 23, 2019
Utilization of echocardiography in Ehlers-Danlos syndromeKristina K Rauser-Foltz, Lois J Starr, Anji T Yetman
American Journal of Medical Genetics. Part A|October 11, 2024
Bullous Lung Disease in Turner Syndrome: An Underrecognized Comorbidity?Stevin Lu, Lois J Starr, Rachel A Taylor, et al.
World Journal for Pediatric & Congenital Heart Surgery|July 5, 2017
Valve-Sparing Root and Total Arch Replacement for Cutis Laxa AortopathyAnji T Yetman, James Hammel, Jennifer N Sanmann, et al.
Clinical Dysmorphology|March 7, 2020
First report of de novo 12q14.2-q23.3 duplication: patient with multiple congenital anomalies, neurodevelopmental delay, and a connective tissue disorder-like phenotype including cutis laxaRohan Khazanchi, Anji T Yetman, Jennifer N Sanmann, et al.
American Journal of Medical Genetics. Part A|March 7, 2019
Patient with anomalous skin pigmentation expands the phenotype of ARID2 loss-of-function disorder, a SWI/SNF-related intellectual disabilityRohan Khazanchi, Carey A Ronspies, Scott C Smith, et al.
Pageof 3

Showing results (1-10 of 30) with videos related to

Sort By:
Pageof 3
American Journal of Medical Genetics. Part A|March 26, 2018
Newly described recessive MYH11 disorder with clinical overlap of Multisystemic smooth muscle dysfunction and Megacystis microcolon hypoperistalsis syndromesAnji T Yetman, Lois J Starr
World Journal for Pediatric & Congenital Heart Surgery|May 26, 2018
Kawasaki Disease in a Patient With Williams SyndromeAleisha M Nabower, Lois J Starr, Jonathan Cramer
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 1, 2024
The Myhre Syndrome Foundation as a global modern support group: The business of rareKate Wears, Angela E Lin, Lois J Starr
Journal for Specialists in Pediatric Nursing : JSPN|February 24, 2018
Autism spectrum disorder and genetic testing: Parental perceptions and decision-makingAlyson E Hanish, Marlene Z Cohen, Lois J Starr
Clinical Dysmorphology|March 24, 2021
Second reported individual with a partial STAG2 deletion: middle interhemispheric variant holoprosencephaly in STAG2-related cohesinopathyDrew M Cratsenberg, Peter J Winningham, Lois J Starr
Congenital Heart Disease|July 23, 2019
Utilization of echocardiography in Ehlers-Danlos syndromeKristina K Rauser-Foltz, Lois J Starr, Anji T Yetman
American Journal of Medical Genetics. Part A|October 11, 2024
Bullous Lung Disease in Turner Syndrome: An Underrecognized Comorbidity?Stevin Lu, Lois J Starr, Rachel A Taylor, et al.
World Journal for Pediatric & Congenital Heart Surgery|July 5, 2017
Valve-Sparing Root and Total Arch Replacement for Cutis Laxa AortopathyAnji T Yetman, James Hammel, Jennifer N Sanmann, et al.
Clinical Dysmorphology|March 7, 2020
First report of de novo 12q14.2-q23.3 duplication: patient with multiple congenital anomalies, neurodevelopmental delay, and a connective tissue disorder-like phenotype including cutis laxaRohan Khazanchi, Anji T Yetman, Jennifer N Sanmann, et al.
American Journal of Medical Genetics. Part A|March 7, 2019
Patient with anomalous skin pigmentation expands the phenotype of ARID2 loss-of-function disorder, a SWI/SNF-related intellectual disabilityRohan Khazanchi, Carey A Ronspies, Scott C Smith, et al.
Pageof 3