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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 syndromes
Anji T Yetman, Lois J Starr
World Journal for Pediatric & Congenital Heart Surgery
|
May 26, 2018
Kawasaki Disease in a Patient With Williams Syndrome
Aleisha 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 rare
Kate 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-making
Alyson 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 cohesinopathy
Drew M Cratsenberg, Peter J Winningham, Lois J Starr
Congenital Heart Disease
|
July 23, 2019
Utilization of echocardiography in Ehlers-Danlos syndrome
Kristina 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 Aortopathy
Anji 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 laxa
Rohan 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 disability
Rohan Khazanchi, Carey A Ronspies, Scott C Smith, et al.
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of 3
Search research articles
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Showing results (1-10 of 30) with videos related to
Sort By:
Page
of 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 syndromes
Anji T Yetman, Lois J Starr
World Journal for Pediatric & Congenital Heart Surgery
|
May 26, 2018
Kawasaki Disease in a Patient With Williams Syndrome
Aleisha 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 rare
Kate 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-making
Alyson 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 cohesinopathy
Drew M Cratsenberg, Peter J Winningham, Lois J Starr
Congenital Heart Disease
|
July 23, 2019
Utilization of echocardiography in Ehlers-Danlos syndrome
Kristina 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 Aortopathy
Anji 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 laxa
Rohan 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 disability
Rohan Khazanchi, Carey A Ronspies, Scott C Smith, et al.
Page
of 3