Search research articles
Contact Us
Filters
Showing results (1-10 of 15) with videos related to
Page
of 2
Sort By:
Dermatology Online Journal
|
February 7, 2022
TP63-related disorders: two case reports and a brief review of the literature
Arti Nanda, Atlal AlLafi, Sabrina Wolf, et al.
Journal of Dermatological Science
|
August 19, 2019
UV-sensitive syndrome: Whole exome sequencing identified a nonsense mutation in the gene UVSSA in two consanguineous pedigrees from Pakistan
Ambreen Ijaz, Sabrina Wolf, Safur Rehman Mandukhail, et al.
Annals of Clinical Biochemistry
|
September 18, 2012
Paediatric reference values for the C-terminal fragment of fibroblast-growth factor-23, sclerostin, bone-specific alkaline phosphatase and isoform 5b of tartrate-resistant acid phosphatase
Dagmar-Christiane Fischer, Anne Mischek, Sabrina Wolf, et al.
Ecology and Evolution
|
April 10, 2019
Release from natural enemies mitigates inbreeding depression in native and invasive <i>Silene latifolia</i> populations
Karin Schrieber, Sabrina Wolf, Catherina Wypior, et al.
Essays in Biochemistry
|
June 7, 2021
Advances in metabolic engineering of Corynebacterium glutamicum to produce high-value active ingredients for food, feed, human health, and well-being
Sabrina Wolf, Judith Becker, Yota Tsuge, et al.
Journal of Inherited Metabolic Disease
|
November 11, 2016
Herpetiform keratitis and palmoplantar hyperkeratosis: warning signs for Richner-Hanhart syndrome
Diogo C Soares, Mariana N Stroparo, Yu C Lian, et al.
American Journal of Medical Genetics. Part A
|
July 2, 2015
Identification of a novel mutation in RIPK4 in a kindred with phenotypic features of Bartsocas-Papas and CHAND syndromes
Benjamin Gollasch, Fitnat Buket Basmanav, Arti Nanda, et al.
Annals of Family Medicine
|
September 22, 2025
Use of an Electronic Health Record Order to Directly Refer Patients With Prediabetes to Community-Based Diabetes Prevention Programs
Karen A Scherr, Cassie D Turner, Sabrina Wolf, et al.
Plos One
|
December 3, 2019
Autosomal-dominant hypotrichosis with woolly hair: Novel gene locus on chromosome 4q35.1-q35.2
Annika E Schlaweck, Rachid Tazi-Ahnini, F Buket Ü Basmanav, et al.
Acta Dermato-Venereologica
|
September 14, 2020
Apparent Missense Variant in COL7A1 Causes a Severe Form of Recessive Dystrophic Epidermolysis Bullosa via Effects on Splicing
Syed Ashraf Uddin, Nicole Cesarato, Aytaj Humbatova, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 15) with videos related to
Sort By:
Page
of 2
Dermatology Online Journal
|
February 7, 2022
TP63-related disorders: two case reports and a brief review of the literature
Arti Nanda, Atlal AlLafi, Sabrina Wolf, et al.
Journal of Dermatological Science
|
August 19, 2019
UV-sensitive syndrome: Whole exome sequencing identified a nonsense mutation in the gene UVSSA in two consanguineous pedigrees from Pakistan
Ambreen Ijaz, Sabrina Wolf, Safur Rehman Mandukhail, et al.
Annals of Clinical Biochemistry
|
September 18, 2012
Paediatric reference values for the C-terminal fragment of fibroblast-growth factor-23, sclerostin, bone-specific alkaline phosphatase and isoform 5b of tartrate-resistant acid phosphatase
Dagmar-Christiane Fischer, Anne Mischek, Sabrina Wolf, et al.
Ecology and Evolution
|
April 10, 2019
Release from natural enemies mitigates inbreeding depression in native and invasive <i>Silene latifolia</i> populations
Karin Schrieber, Sabrina Wolf, Catherina Wypior, et al.
Essays in Biochemistry
|
June 7, 2021
Advances in metabolic engineering of Corynebacterium glutamicum to produce high-value active ingredients for food, feed, human health, and well-being
Sabrina Wolf, Judith Becker, Yota Tsuge, et al.
Journal of Inherited Metabolic Disease
|
November 11, 2016
Herpetiform keratitis and palmoplantar hyperkeratosis: warning signs for Richner-Hanhart syndrome
Diogo C Soares, Mariana N Stroparo, Yu C Lian, et al.
American Journal of Medical Genetics. Part A
|
July 2, 2015
Identification of a novel mutation in RIPK4 in a kindred with phenotypic features of Bartsocas-Papas and CHAND syndromes
Benjamin Gollasch, Fitnat Buket Basmanav, Arti Nanda, et al.
Annals of Family Medicine
|
September 22, 2025
Use of an Electronic Health Record Order to Directly Refer Patients With Prediabetes to Community-Based Diabetes Prevention Programs
Karen A Scherr, Cassie D Turner, Sabrina Wolf, et al.
Plos One
|
December 3, 2019
Autosomal-dominant hypotrichosis with woolly hair: Novel gene locus on chromosome 4q35.1-q35.2
Annika E Schlaweck, Rachid Tazi-Ahnini, F Buket Ü Basmanav, et al.
Acta Dermato-Venereologica
|
September 14, 2020
Apparent Missense Variant in COL7A1 Causes a Severe Form of Recessive Dystrophic Epidermolysis Bullosa via Effects on Splicing
Syed Ashraf Uddin, Nicole Cesarato, Aytaj Humbatova, et al.
Page
of 2