Search research articles
Contact Us
Filters
Showing results (291-300 of 347) with videos related to
Page
of 35
Sort By:
Journal of Biological Regulators and Homeostatic Agents
|
October 1, 2020
Cardiac malformations in children with congenital hypothyroidism
M Scavone, V Tallarico, E Stefanelli, et al.
The British Journal of Dermatology
|
January 17, 2007
Association between cutaneous melanoma, Breslow thickness and vitamin D receptor BsmI polymorphism
C Santonocito, R Capizzi, P Concolino, et al.
Journal of Biological Regulators and Homeostatic Agents
|
October 1, 2020
Hypertension in childhood
G Ceravolo, M Fusco, C Salpietro, et al.
Genes
|
September 27, 2025
Detection of Clinically Significant BRCA Large Genomic Rearrangements in FFPE Ovarian Cancer Samples: A Comparative NGS Study
Alessia Perrucci, Maria De Bonis, Giulia Maneri, et al.
Stem Cell Research
|
June 9, 2018
iPSC-derived neurons of CREBBP- and EP300-mutated Rubinstein-Taybi syndrome patients show morphological alterations and hypoexcitability
Valentina Alari, Silvia Russo, Benedetta Terragni, et al.
Journal of Biological Regulators and Homeostatic Agents
|
October 22, 2019
Alport's syndrome
V Bruni, M Petrisano, F Tarsitano, et al.
American Journal of Physiology. Endocrinology and Metabolism
|
September 7, 2006
Epithelial lining fluid free IGF-I-to-PAPP-A ratio is associated with bronchopulmonary dysplasia in preterm infants
Ettore Capoluongo, Franco Ameglio, Paola Lulli, et al.
Expert Review of Molecular Diagnostics
|
August 27, 2015
Clinical impact on ovarian cancer patients of massive parallel sequencing for BRCA mutation detection: the experience at Gemelli hospital and a literature review
Angelo Minucci, Giovanni Scambia, Concetta Santonocito, et al.
Genes
|
June 28, 2023
Identification and Molecular Characterization of a Novel Large-Scale Variant (Exons 4_18 Loss) in the LDLR Gene as a Cause of Familial Hypercholesterolaemia in an Italian Family
Paola Concolino, Elisa De Paolis, Simona Moffa, et al.
Annals of Laboratory Medicine
|
June 3, 2024
Identification of a False-positive Multiplex Ligationdependent Probe Amplification Result in <i>BRCA1</i> Using a Copy Number Variation Algorithm Under Development for a Commercial Next-Generation Sequencing-based Homologous Recombination Deficiency Assay
Paola Concolino, Elisa De Paolis, Martina Rinelli, et al.
Page
of 35
Search research articles
Search
Showing results (291-300 of 347) with videos related to
Sort By:
Page
of 35
Journal of Biological Regulators and Homeostatic Agents
|
October 1, 2020
Cardiac malformations in children with congenital hypothyroidism
M Scavone, V Tallarico, E Stefanelli, et al.
The British Journal of Dermatology
|
January 17, 2007
Association between cutaneous melanoma, Breslow thickness and vitamin D receptor BsmI polymorphism
C Santonocito, R Capizzi, P Concolino, et al.
Journal of Biological Regulators and Homeostatic Agents
|
October 1, 2020
Hypertension in childhood
G Ceravolo, M Fusco, C Salpietro, et al.
Genes
|
September 27, 2025
Detection of Clinically Significant BRCA Large Genomic Rearrangements in FFPE Ovarian Cancer Samples: A Comparative NGS Study
Alessia Perrucci, Maria De Bonis, Giulia Maneri, et al.
Stem Cell Research
|
June 9, 2018
iPSC-derived neurons of CREBBP- and EP300-mutated Rubinstein-Taybi syndrome patients show morphological alterations and hypoexcitability
Valentina Alari, Silvia Russo, Benedetta Terragni, et al.
Journal of Biological Regulators and Homeostatic Agents
|
October 22, 2019
Alport's syndrome
V Bruni, M Petrisano, F Tarsitano, et al.
American Journal of Physiology. Endocrinology and Metabolism
|
September 7, 2006
Epithelial lining fluid free IGF-I-to-PAPP-A ratio is associated with bronchopulmonary dysplasia in preterm infants
Ettore Capoluongo, Franco Ameglio, Paola Lulli, et al.
Expert Review of Molecular Diagnostics
|
August 27, 2015
Clinical impact on ovarian cancer patients of massive parallel sequencing for BRCA mutation detection: the experience at Gemelli hospital and a literature review
Angelo Minucci, Giovanni Scambia, Concetta Santonocito, et al.
Genes
|
June 28, 2023
Identification and Molecular Characterization of a Novel Large-Scale Variant (Exons 4_18 Loss) in the LDLR Gene as a Cause of Familial Hypercholesterolaemia in an Italian Family
Paola Concolino, Elisa De Paolis, Simona Moffa, et al.
Annals of Laboratory Medicine
|
June 3, 2024
Identification of a False-positive Multiplex Ligationdependent Probe Amplification Result in <i>BRCA1</i> Using a Copy Number Variation Algorithm Under Development for a Commercial Next-Generation Sequencing-based Homologous Recombination Deficiency Assay
Paola Concolino, Elisa De Paolis, Martina Rinelli, et al.
Page
of 35