Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Patricia Robbins‐Furman"'
Autor:
Ko-Lin Wu, Rebeca Alegria, Jazzlyn Gonzalez, Harrison Hu, Haocen Wang, Robin Page, Patricia Robbins-Furman, Ping Ma, Tung-Sung Tseng, Lei-Shih Chen
Publikováno v:
JMIR mHealth and uHealth, Vol 9, Iss 10, p e30404 (2021)
BackgroundPrenatal genetic testing is an essential part of routine prenatal care. Yet, obstetricians often lack the time to provide comprehensive prenatal genetic testing education to their patients. Pregnant women lack prenatal genetic testing knowl
Externí odkaz:
https://doaj.org/article/084ce14f982248dea669d69a95507adf
Autor:
Alyssa Grygiel, Felicia Ikolo, Raphielle Stephen, Dawnell Bleasdille, Patricia Robbins‐Furman, Beverly Nelson, Andrew K. Sobering, Sarah H. Elsea
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 1, Pp n/a-n/a (2021)
Abstract Background Grenada is a small, resource‐limited Caribbean country with a high incidence of sickle cell disease (SCD). Since little is known about the challenges facing individuals living with SCD in the West Indies, we sought to assess bar
Externí odkaz:
https://doaj.org/article/216e0adf874f49e0a45c1c511ca3ebc9
Autor:
Melodie Tedross, Haocen Wang, Claire Heigl‐Maza, Rebecca Russell, Christine Young, Justin Kramer, Denise Martinez, Wei‐Ju Chen, Patricia Robbins‐Furman, Robin Page, Nora Montalvo‐Liendo, Lei‐Shih Chen
Publikováno v:
Journal of Genetic Counseling.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b5016c285fd84bf1ddb69a36d4cd4749
https://doi.org/10.1002/jgc4.1696
https://doi.org/10.1002/jgc4.1696
Autor:
Haocen Wang, Robin Page, Daniela Lopez, Samruddhi Arkatkar, Christine Young, Denise Martinez, Patricia Robbins-Furman, Nora Montalvo-Liendo, Lei-Shih Chen
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics. 24(8)
There are, currently, conflicting opinions about the adoption of exome sequencing (ES) into the standard newborn screening program. This study aimed to explore the views of pregnant Latinas, a hard-to-reach, underserved, and understudied population,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59916e2dddde16e6ccfecba1e826b3a1
https://pubmed.ncbi.nlm.nih.gov/35579624
https://pubmed.ncbi.nlm.nih.gov/35579624
Autor:
Patricia Robbins-Furman, Ping Ma, Ko-Lin Wu, Harrison Hu, Jazzlyn Gonzalez, Lei-Shih Chen, Robin L. Page, Rebeca Alegria, Haocen Wang, Tung-Sung Tseng
Publikováno v:
JMIR mHealth and uHealth
Background Prenatal genetic testing is an essential part of routine prenatal care. Yet, obstetricians often lack the time to provide comprehensive prenatal genetic testing education to their patients. Pregnant women lack prenatal genetic testing know
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2991628051114752c148e61362ffbe2
http://europepmc.org/articles/PMC8554671
http://europepmc.org/articles/PMC8554671
Autor:
Ko-Lin Wu, Rebeca Alegria, Jazzlyn Gonzalez, Harrison Hu, Haocen Wang, Robin Page, Patricia Robbins-Furman, Ping Ma, Tung-Sung Tseng, Lei-Shih Chen
BACKGROUND Prenatal genetic testing is an essential part of routine prenatal care. Yet, obstetricians often lack the time to provide comprehensive prenatal genetic testing education to their patients. Pregnant women lack prenatal genetic testing know
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49f21dffcd84f3e6c8f33ca64ed8d2d9
https://doi.org/10.2196/preprints.30404
https://doi.org/10.2196/preprints.30404
Autor:
Alyssa Grygiel, Felicia Ikolo, Raphielle Stephen, Dawnell Bleasdille, Patricia Robbins‐Furman, Beverly Nelson, Andrew K. Sobering, Sarah H. Elsea
Publikováno v:
Mol Genet Genomic Med
The cover image is based on the Original Article Sickle cell disease in Grenada: Quality of life and barriers to care by Alyssa Grygiel et al., https://doi.org/10.1002/mgg3.1567. Image credit: Jack Nelson and Lucia Garces Torres. [Image: see text]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d77f29172bde4b961c03c4dee96494b5
https://europepmc.org/articles/PMC7963422/
https://europepmc.org/articles/PMC7963422/
Autor:
Raphielle Stephen, Dawnell Bleasdille, Beverly Nelson, Felicia Ikolo, Patricia Robbins-Furman, Alyssa Grygiel, Sarah H. Elsea, Andrew K. Sobering
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 1, Pp n/a-n/a (2021)
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine
Background Grenada is a small, resource‐limited Caribbean country with a high incidence of sickle cell disease (SCD). Since little is known about the challenges facing individuals living with SCD in the West Indies, we sought to assess barriers to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3062a76a6509d5d887eecdaedd55e1f
https://doaj.org/article/216e0adf874f49e0a45c1c511ca3ebc9
https://doaj.org/article/216e0adf874f49e0a45c1c511ca3ebc9
Autor:
Patricia Robbins-Furman, Denise Martinez, Nora Montalvo-Liendo, Haocen Wang, Christine Young, Wei-Ju Chen, Robin L. Page, Lei-Shih Chen, Brandon Williamson
Publikováno v:
Obstetrics and gynecology. 138(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba911674833114cdd6f0d47b4e8d9b1d
https://pubmed.ncbi.nlm.nih.gov/34259471
https://pubmed.ncbi.nlm.nih.gov/34259471
Autor:
S. Shahrukh Hashmi, Lorraine Potocki, Michael J. Gambello, Susan K. Peterson, Rebecca D. Carter, Linda Ewing-Cobbs, Patricia Robbins-Furman, Marianna Raia
Publikováno v:
Journal of Genetic Counseling. 22:633-642
Potocki-Lupski syndrome (PTLS) or duplication 17p11.2 syndrome is a newly characterized condition causing a variety of health problems with variable severity, including failure to thrive in infancy and childhood, hypotonia, structural heart anomalies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e36e583383b707ecd38ea31db43a6dfb
https://doi.org/10.1007/s10897-013-9602-6
https://doi.org/10.1007/s10897-013-9602-6