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Clinical genetics

Showing results (561-570 of 7,173) with videos related to

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Clinical Genetics|March 24, 2022
El-Hattab-Alkuraya syndrome caused by biallelic WDR45B pathogenic variants: Further delineation of the phenotype and genotypeMohammed Almannai, Dana Marafi, Ghada M H Abdel-Salam, et al.
Clinical Genetics|March 30, 2022
Expanding genotypic and phenotypic spectrums of LTBP3 variants in dental anomalies and short stature syndromePiranit Kantaputra, Yeliz Guven, Tugba Kalayci, et al.
Clinical Genetics|March 5, 2022
A novel homozygous variant in COX5A causes an attenuated phenotype with failure to thrive, lactic acidosis, hypoglycemia, and short statureAlessandra Torraco, Silvia Morlino, Teresa Rizza, et al.
Clinical Genetics|February 11, 2000
Utility of the predictors of coronary heart disease mortality in a longitudinal study of elderly Finnish men aged 65 to 84 years is dependent on context defined by Apo E genotype and area of residenceJ H Stengård, S L Kardia, M Tervahauta, et al.
Clinical Genetics|February 11, 2000
Genetic and segregation analysis of congenital cataract in the Indian populationVanita, J R Singh, D Singh
Clinical Genetics|May 20, 1999
An extra idic(21)(q22.1) in a child with some features of Down's syndromeM Gütiérrez-Angulo, A L Ramos, N Dávalos, et al.
Clinical Genetics|August 18, 1999
Chromosome 11q13 and atopic asthmaC N Adra, X Q Mao, H Kawada, et al.
Clinical Genetics|August 18, 1999
Schizophrenia susceptibility gene locus at Xp22.3J Milunsky, X L Huang, H E Wyandt, et al.
Clinical Genetics|August 18, 1999
Assessment of RS1 in X-linked juvenile retinoschisis and sporadic senile retinoschisisA Gehrig, K White, B Lorenz, et al.
Clinical Genetics|August 18, 1999
Cloning of translocation breakpoints associated with Shwachman syndrome and identification of a candidate geneS Ikegawa, M Masuno, Y Kumano, et al.
Pageof 718

Showing results (561-570 of 7,173) with videos related to

Sort By:
Pageof 718
Clinical Genetics|March 24, 2022
El-Hattab-Alkuraya syndrome caused by biallelic WDR45B pathogenic variants: Further delineation of the phenotype and genotypeMohammed Almannai, Dana Marafi, Ghada M H Abdel-Salam, et al.
Clinical Genetics|March 30, 2022
Expanding genotypic and phenotypic spectrums of LTBP3 variants in dental anomalies and short stature syndromePiranit Kantaputra, Yeliz Guven, Tugba Kalayci, et al.
Clinical Genetics|March 5, 2022
A novel homozygous variant in COX5A causes an attenuated phenotype with failure to thrive, lactic acidosis, hypoglycemia, and short statureAlessandra Torraco, Silvia Morlino, Teresa Rizza, et al.
Clinical Genetics|February 11, 2000
Utility of the predictors of coronary heart disease mortality in a longitudinal study of elderly Finnish men aged 65 to 84 years is dependent on context defined by Apo E genotype and area of residenceJ H Stengård, S L Kardia, M Tervahauta, et al.
Clinical Genetics|February 11, 2000
Genetic and segregation analysis of congenital cataract in the Indian populationVanita, J R Singh, D Singh
Clinical Genetics|May 20, 1999
An extra idic(21)(q22.1) in a child with some features of Down's syndromeM Gütiérrez-Angulo, A L Ramos, N Dávalos, et al.
Clinical Genetics|August 18, 1999
Chromosome 11q13 and atopic asthmaC N Adra, X Q Mao, H Kawada, et al.
Clinical Genetics|August 18, 1999
Schizophrenia susceptibility gene locus at Xp22.3J Milunsky, X L Huang, H E Wyandt, et al.
Clinical Genetics|August 18, 1999
Assessment of RS1 in X-linked juvenile retinoschisis and sporadic senile retinoschisisA Gehrig, K White, B Lorenz, et al.
Clinical Genetics|August 18, 1999
Cloning of translocation breakpoints associated with Shwachman syndrome and identification of a candidate geneS Ikegawa, M Masuno, Y Kumano, et al.
Pageof 718