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Vector Borne and Zoonotic Diseases (Larchmont, N.Y.)
|
March 19, 2011
Molecular detection and identification of Rickettsia species in Ixodes pacificus in California
Jimmy Ninh Phan, Casey Roy Lu, William Garrett Bender, et al.
The Einstein Journal of Biology and Medicine : EJBM
|
November 11, 2014
Perceptions of an implantable cardioverter-defibrillator: A qualitative study of families with a history of sudden life-threatening cardiac events and recommendations to improve care
Jarrett Linder, Nadia Hidayatallah, Marina Stolerman, et al.
Journal of Genetic Counseling
|
February 20, 2009
Diversity in genetic counseling: strategies from the LEND network
Ashley Hatchel, Janet Willis, Catherine Reiser, et al.
Journal of Pediatric Hematology/Oncology
|
April 4, 2012
Hepatoblastoma in a mosaic trisomy 18 patient
Elaine Maria Pereira, Robert Marion, K H Ramesh, et al.
Clinical Nutrition ESPEN
|
March 27, 2018
Hyperlipidemia secondary to acitretin therapy for lamellar ichthyosis associated with a NIPAL4 mutation improves on a plant-based diet and relapses on a standard Western diet
Jonathan C Lin, Daniele Massera, Mohammad Ghalib, et al.
Journal of Community Genetics
|
October 6, 2022
Genetic screening of relatives of decedents experiencing sudden unexpected death: medical examiner's office referrals to a multi-disciplinary cardiogenetics program
Tamar Siskind, Nori Williams, Monisha Sebastin, et al.
Molecular Cytogenetics
|
December 9, 2014
A de novo 10.79 Mb interstitial deletion at 2q13q14.2 involving PAX8 causing hypothyroidism and mullerian agenesis: a novel case report and literature review
Deqiong Ma, Robert Marion, Netra Prasad Punjabi, et al.
Cardiovascular Pathology : the Official Journal of the Society for Cardiovascular Pathology
|
October 4, 2018
Phenotypic variations in carriers of predicted protein-truncating genetic variants in MYBPC3: an autopsy-based case series
Nori Williams, Robert Marion, Thomas V McDonald, et al.
Neurogenetics
|
January 6, 2012
Genotype-phenotype correlation in interstitial 6q deletions: a report of 12 new cases
Jill A Rosenfeld, Dina Amrom, Eva Andermann, et al.
American Journal of Human Genetics
|
March 5, 2013
Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes
Maria Delio, Tingwei Guo, Donna M McDonald-McGinn, et al.
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Search research articles
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Showing results (11-20 of 20) with videos related to
Sort By:
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You have reached the last page of results.
This site can display upto 20 results.
Vector Borne and Zoonotic Diseases (Larchmont, N.Y.)
|
March 19, 2011
Molecular detection and identification of Rickettsia species in Ixodes pacificus in California
Jimmy Ninh Phan, Casey Roy Lu, William Garrett Bender, et al.
The Einstein Journal of Biology and Medicine : EJBM
|
November 11, 2014
Perceptions of an implantable cardioverter-defibrillator: A qualitative study of families with a history of sudden life-threatening cardiac events and recommendations to improve care
Jarrett Linder, Nadia Hidayatallah, Marina Stolerman, et al.
Journal of Genetic Counseling
|
February 20, 2009
Diversity in genetic counseling: strategies from the LEND network
Ashley Hatchel, Janet Willis, Catherine Reiser, et al.
Journal of Pediatric Hematology/Oncology
|
April 4, 2012
Hepatoblastoma in a mosaic trisomy 18 patient
Elaine Maria Pereira, Robert Marion, K H Ramesh, et al.
Clinical Nutrition ESPEN
|
March 27, 2018
Hyperlipidemia secondary to acitretin therapy for lamellar ichthyosis associated with a NIPAL4 mutation improves on a plant-based diet and relapses on a standard Western diet
Jonathan C Lin, Daniele Massera, Mohammad Ghalib, et al.
Journal of Community Genetics
|
October 6, 2022
Genetic screening of relatives of decedents experiencing sudden unexpected death: medical examiner's office referrals to a multi-disciplinary cardiogenetics program
Tamar Siskind, Nori Williams, Monisha Sebastin, et al.
Molecular Cytogenetics
|
December 9, 2014
A de novo 10.79 Mb interstitial deletion at 2q13q14.2 involving PAX8 causing hypothyroidism and mullerian agenesis: a novel case report and literature review
Deqiong Ma, Robert Marion, Netra Prasad Punjabi, et al.
Cardiovascular Pathology : the Official Journal of the Society for Cardiovascular Pathology
|
October 4, 2018
Phenotypic variations in carriers of predicted protein-truncating genetic variants in MYBPC3: an autopsy-based case series
Nori Williams, Robert Marion, Thomas V McDonald, et al.
Neurogenetics
|
January 6, 2012
Genotype-phenotype correlation in interstitial 6q deletions: a report of 12 new cases
Jill A Rosenfeld, Dina Amrom, Eva Andermann, et al.
American Journal of Human Genetics
|
March 5, 2013
Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes
Maria Delio, Tingwei Guo, Donna M McDonald-McGinn, et al.
Page
of 2