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American Journal of Medical Genetics. Part A
|
April 4, 2017
Nonsense pathogenic variants in exon 1 of PHOX2B lead to translational reinitiation in congenital central hypoventilation syndrome
Jacob T Cain, Dae I Kim, Megan Quast, et al.
American Journal of Medical Genetics. Part A
|
September 25, 2014
Perinatal features of the RASopathies: Noonan syndrome, cardiofaciocutaneous syndrome and Costello syndrome
Angela Myers, Jonathan A Bernstein, Marie-Luise Brennan, et al.
The American Journal of Medicine
|
October 24, 2024
Salary Equity Among Subspecialty Fellows: A Call to Action
Solomon Liao, Alpesh N Amin, Steven Barczi, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)
|
July 24, 2015
Mutation in GM2A Leads to a Progressive Chorea-dementia Syndrome
Mustafa A Salih, Mohammed Z Seidahmed, Heba Y El Khashab, et al.
Neurology. Genetics
|
May 26, 2016
Homozygous GNAL mutation associated with familial childhood-onset generalized dystonia
Ikuo Masuho, Mingyan Fang, Chunyu Geng, et al.
The Journal of Pediatrics
|
November 7, 2025
Reply
YoungNa Lee-Kim, Lisa DelSignore, Nicholas J Antos, et al.
American Journal of Medical Genetics. Part A
|
July 29, 2018
Nonreentrant atrial tachycardia occurs independently of hypertrophic cardiomyopathy in RASopathy patients
Mark D Levin, Sulagna C Saitta, Karen W Gripp, et al.
The Journal of Pediatrics
|
July 30, 2025
A Rising Tide Lifts All Boats: The Role of the Subspecialist in Recruitment into Pediatrics
YoungNa Lee-Kim, Lisa DelSignore, Nicholas J Antos, et al.
Pediatric Research
|
November 14, 2022
Humoral and cellular response to the COVID-19 vaccine in immunocompromised children
Heather A Morgans, Todd Bradley, Linda Flebbe-Rehwaldt, et al.
Pediatrics
|
October 20, 2021
Achieving Entrustable Professional Activities During Fellowship
Pnina G Weiss, Alan Schwartz, Carol L Carraccio, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 43) with videos related to
Sort By:
Page
of 5
American Journal of Medical Genetics. Part A
|
April 4, 2017
Nonsense pathogenic variants in exon 1 of PHOX2B lead to translational reinitiation in congenital central hypoventilation syndrome
Jacob T Cain, Dae I Kim, Megan Quast, et al.
American Journal of Medical Genetics. Part A
|
September 25, 2014
Perinatal features of the RASopathies: Noonan syndrome, cardiofaciocutaneous syndrome and Costello syndrome
Angela Myers, Jonathan A Bernstein, Marie-Luise Brennan, et al.
The American Journal of Medicine
|
October 24, 2024
Salary Equity Among Subspecialty Fellows: A Call to Action
Solomon Liao, Alpesh N Amin, Steven Barczi, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)
|
July 24, 2015
Mutation in GM2A Leads to a Progressive Chorea-dementia Syndrome
Mustafa A Salih, Mohammed Z Seidahmed, Heba Y El Khashab, et al.
Neurology. Genetics
|
May 26, 2016
Homozygous GNAL mutation associated with familial childhood-onset generalized dystonia
Ikuo Masuho, Mingyan Fang, Chunyu Geng, et al.
The Journal of Pediatrics
|
November 7, 2025
Reply
YoungNa Lee-Kim, Lisa DelSignore, Nicholas J Antos, et al.
American Journal of Medical Genetics. Part A
|
July 29, 2018
Nonreentrant atrial tachycardia occurs independently of hypertrophic cardiomyopathy in RASopathy patients
Mark D Levin, Sulagna C Saitta, Karen W Gripp, et al.
The Journal of Pediatrics
|
July 30, 2025
A Rising Tide Lifts All Boats: The Role of the Subspecialist in Recruitment into Pediatrics
YoungNa Lee-Kim, Lisa DelSignore, Nicholas J Antos, et al.
Pediatric Research
|
November 14, 2022
Humoral and cellular response to the COVID-19 vaccine in immunocompromised children
Heather A Morgans, Todd Bradley, Linda Flebbe-Rehwaldt, et al.
Pediatrics
|
October 20, 2021
Achieving Entrustable Professional Activities During Fellowship
Pnina G Weiss, Alan Schwartz, Carol L Carraccio, et al.
Page
of 5