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Annals of Human Genetics
|
April 13, 2019
A novel SLC12A1 mutation in Bedouin kindred with antenatal Bartter syndrome type I
Daniel Halperin, Vadim Dolgin, Michael Geylis, et al.
Journal of Pediatric Surgery
|
June 21, 2011
A comparison of the cleft lift procedure vs wide excision and packing for the treatment of pilonidal disease in adolescents
Amir S Gendy, Richard D Glick, Andrew R Hong, et al.
Journal of Pediatric Oncology Nursing : Official Journal of the Association of Pediatric Oncology Nurses
|
April 29, 2009
Qualitative analysis of the role of culture in coping themes of Latina and European American mothers of children with cancer
Alexis L Johns, Alyssa A Oland, Ernest R Katz, et al.
European Journal of Human Genetics : EJHG
|
June 13, 2019
DEGS1 variant causes neurological disorder
Vadim Dolgin, Rachel Straussberg, Ruijuan Xu, et al.
Clinical Genetics
|
July 4, 2020
Pituitary stalk interruption syndrome broadens the clinical spectrum of the TTC26 ciliopathy
Odeya David, Marina Eskin-Schwartz, Galina Ling, et al.
Clinical Genetics
|
October 10, 2023
CLDN1 Arg81His founder variant causes ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis (ILVASC) syndrome in Moroccan Jews
Marina Eskin-Schwartz, Vadim Dolgin, Elena Didkovsky, et al.
The New England Journal of Medicine
|
April 2, 1981
Identification of patients with cholesterol or pigment gallstones by discriminant analysis of radiographic features
S M Dolgin, J S Schwartz, H Y Kressel, et al.
HGG Advances
|
June 24, 2026
A lethal form of ASCC3 disease: severe global developmental delay, axial hypotonia, hypoplasia of corpus callosum, hypothyroidism and micropenis
Ginat Narkis, Vadim Dolgin, Sufa Sued-Hendrickson, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
January 30, 2013
Specificity of problem-solving skills training in mothers of children newly diagnosed with cancer: results of a multisite randomized clinical trial
Olle Jane Z Sahler, Michael J Dolgin, Sean Phipps, et al.
European Journal of Human Genetics : EJHG
|
March 3, 2024
Heterozygous THBS2 pathogenic variant causes Ehlers-Danlos syndrome with prominent vascular features in humans and mice
Noam Hadar, Omri Porgador, Idan Cohen, et al.
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of 20
Search research articles
Search
Showing results (151-160 of 199) with videos related to
Sort By:
Page
of 20
Annals of Human Genetics
|
April 13, 2019
A novel SLC12A1 mutation in Bedouin kindred with antenatal Bartter syndrome type I
Daniel Halperin, Vadim Dolgin, Michael Geylis, et al.
Journal of Pediatric Surgery
|
June 21, 2011
A comparison of the cleft lift procedure vs wide excision and packing for the treatment of pilonidal disease in adolescents
Amir S Gendy, Richard D Glick, Andrew R Hong, et al.
Journal of Pediatric Oncology Nursing : Official Journal of the Association of Pediatric Oncology Nurses
|
April 29, 2009
Qualitative analysis of the role of culture in coping themes of Latina and European American mothers of children with cancer
Alexis L Johns, Alyssa A Oland, Ernest R Katz, et al.
European Journal of Human Genetics : EJHG
|
June 13, 2019
DEGS1 variant causes neurological disorder
Vadim Dolgin, Rachel Straussberg, Ruijuan Xu, et al.
Clinical Genetics
|
July 4, 2020
Pituitary stalk interruption syndrome broadens the clinical spectrum of the TTC26 ciliopathy
Odeya David, Marina Eskin-Schwartz, Galina Ling, et al.
Clinical Genetics
|
October 10, 2023
CLDN1 Arg81His founder variant causes ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis (ILVASC) syndrome in Moroccan Jews
Marina Eskin-Schwartz, Vadim Dolgin, Elena Didkovsky, et al.
The New England Journal of Medicine
|
April 2, 1981
Identification of patients with cholesterol or pigment gallstones by discriminant analysis of radiographic features
S M Dolgin, J S Schwartz, H Y Kressel, et al.
HGG Advances
|
June 24, 2026
A lethal form of ASCC3 disease: severe global developmental delay, axial hypotonia, hypoplasia of corpus callosum, hypothyroidism and micropenis
Ginat Narkis, Vadim Dolgin, Sufa Sued-Hendrickson, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
January 30, 2013
Specificity of problem-solving skills training in mothers of children newly diagnosed with cancer: results of a multisite randomized clinical trial
Olle Jane Z Sahler, Michael J Dolgin, Sean Phipps, et al.
European Journal of Human Genetics : EJHG
|
March 3, 2024
Heterozygous THBS2 pathogenic variant causes Ehlers-Danlos syndrome with prominent vascular features in humans and mice
Noam Hadar, Omri Porgador, Idan Cohen, et al.
Page
of 20