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Genes
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January 21, 2023
Improved Outcomes in Patients with 22q11.2 Deletion Syndrome and Diagnosis of Interrupted Aortic Arch Prior to Birth Hospital Discharge, a Retrospective Study
Hayley A Ron, Terrence Blaine Crowley, Yichuan Liu, et al.
Genes
|
January 21, 2023
Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions
Natalie Blagowidow, Beata Nowakowska, Erica Schindewolf, et al.
American Journal of Obstetrics and Gynecology
|
June 24, 2024
Amniocentesis in pregnancies at or beyond 24 weeks: an international multicenter study
Roni Zemet, Mohamad Ali Maktabi, Alexandra Tinfow, et al.
JCI Insight
|
May 8, 2023
Lymphatic disorders caused by mosaic, activating KRAS variants respond to MEK inhibition
Sarah E Sheppard, Michael E March, Christoph Seiler, et al.
Blood Advances
|
October 28, 2022
The impact of in utero transfusions on perinatal outcomes in patients with alpha thalassemia major: the UCSF registry
Marisa E Schwab, Billie R Lianoglou, Dawn Gano, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 2, 2023
Updated clinical practice recommendations for managing children with 22q11.2 deletion syndrome
Sólveig Óskarsdóttir, Erik Boot, Terrence Blaine Crowley, et al.
Genes
|
July 27, 2024
Expanding Genetic Counselor Roles: A Model for Global Research Development
Colleen C Muraresku, Elizabeth M McCormick, Lydia Rockart, et al.
American Journal of Obstetrics and Gynecology
|
September 17, 2023
Prenatal vs postnatal diagnosis of 22q11.2 deletion syndrome: cardiac and noncardiac outcomes through 1 year of age
Lindsay R Freud, Stephanie Galloway, T Blaine Crowley, et al.
Science (New York, N.Y.)
|
May 2, 2024
Risk of meningomyelocele mediated by the common 22q11.2 deletion
Keng Ioi Vong, Sangmoon Lee, Kit Sing Au, et al.
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of 3
Search research articles
Search
Showing results (21-30 of 29) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 29 results.
Genes
|
January 21, 2023
Improved Outcomes in Patients with 22q11.2 Deletion Syndrome and Diagnosis of Interrupted Aortic Arch Prior to Birth Hospital Discharge, a Retrospective Study
Hayley A Ron, Terrence Blaine Crowley, Yichuan Liu, et al.
Genes
|
January 21, 2023
Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions
Natalie Blagowidow, Beata Nowakowska, Erica Schindewolf, et al.
American Journal of Obstetrics and Gynecology
|
June 24, 2024
Amniocentesis in pregnancies at or beyond 24 weeks: an international multicenter study
Roni Zemet, Mohamad Ali Maktabi, Alexandra Tinfow, et al.
JCI Insight
|
May 8, 2023
Lymphatic disorders caused by mosaic, activating KRAS variants respond to MEK inhibition
Sarah E Sheppard, Michael E March, Christoph Seiler, et al.
Blood Advances
|
October 28, 2022
The impact of in utero transfusions on perinatal outcomes in patients with alpha thalassemia major: the UCSF registry
Marisa E Schwab, Billie R Lianoglou, Dawn Gano, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 2, 2023
Updated clinical practice recommendations for managing children with 22q11.2 deletion syndrome
Sólveig Óskarsdóttir, Erik Boot, Terrence Blaine Crowley, et al.
Genes
|
July 27, 2024
Expanding Genetic Counselor Roles: A Model for Global Research Development
Colleen C Muraresku, Elizabeth M McCormick, Lydia Rockart, et al.
American Journal of Obstetrics and Gynecology
|
September 17, 2023
Prenatal vs postnatal diagnosis of 22q11.2 deletion syndrome: cardiac and noncardiac outcomes through 1 year of age
Lindsay R Freud, Stephanie Galloway, T Blaine Crowley, et al.
Science (New York, N.Y.)
|
May 2, 2024
Risk of meningomyelocele mediated by the common 22q11.2 deletion
Keng Ioi Vong, Sangmoon Lee, Kit Sing Au, et al.
Page
of 3