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Showing results (501-510 of 590) with videos related to

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American Journal of Human Genetics|June 25, 2011
Using VAAST to identify an X-linked disorder resulting in lethality in male infants due to N-terminal acetyltransferase deficiencyAlan F Rope, Kai Wang, Rune Evjenth, et al.
Molecular Psychiatry|July 20, 2011
Genome-wide linkage analysis of 972 bipolar pedigrees using single-nucleotide polymorphismsJ A Badner, D Koller, T Foroud, et al.
Science Translational Medicine|December 13, 2023
Short-course combination treatment for experimental chronic Chagas diseaseSilvia González, Richard J Wall, John Thomas, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 4, 2021
Is Persistent Motor or Vocal Tic Disorder a Milder Form of Tourette Syndrome?Karla Claudio-Campos, Daniel Stevens, Sang-Wahn Koo, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
Distinct patterns of <i>de novo</i> coding variants contribute to Tourette Syndrome etiologyLingyu Zhan, Dongmei Yu, Franjo Ivankovic, et al.
Science Translational Medicine|December 13, 2023
DNDI-6174 is a preclinical candidate for visceral leishmaniasis that targets the cytochrome bc<sub>1</sub>Stéphanie Braillard, Martine Keenan, Karen J Breese, et al.
Nature Biomedical Engineering|August 19, 2022
Diagnosis of paediatric tuberculosis by optically detecting two virulence factors on extracellular vesicles in blood samplesWenshu Zheng, Sylvia M LaCourse, Bofan Song, et al.
Nature Genetics|February 11, 2022
GestaltMatcher facilitates rare disease matching using facial phenotype descriptorsTzung-Chien Hsieh, Aviram Bar-Haim, Shahida Moosa, et al.
Nature Genetics|August 7, 2023
PhenoScore quantifies phenotypic variation for rare genetic diseases by combining facial analysis with other clinical features using a machine-learning frameworkAlexander J M Dingemans, Max Hinne, Kim M G Truijen, et al.
American Journal of Human Genetics|December 7, 2015
TAF1 Variants Are Associated with Dysmorphic Features, Intellectual Disability, and Neurological ManifestationsJason A O'Rawe, Yiyang Wu, Max J Dörfel, et al.
Pageof 59

Showing results (501-510 of 590) with videos related to

Sort By:
Pageof 59
American Journal of Human Genetics|June 25, 2011
Using VAAST to identify an X-linked disorder resulting in lethality in male infants due to N-terminal acetyltransferase deficiencyAlan F Rope, Kai Wang, Rune Evjenth, et al.
Molecular Psychiatry|July 20, 2011
Genome-wide linkage analysis of 972 bipolar pedigrees using single-nucleotide polymorphismsJ A Badner, D Koller, T Foroud, et al.
Science Translational Medicine|December 13, 2023
Short-course combination treatment for experimental chronic Chagas diseaseSilvia González, Richard J Wall, John Thomas, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 4, 2021
Is Persistent Motor or Vocal Tic Disorder a Milder Form of Tourette Syndrome?Karla Claudio-Campos, Daniel Stevens, Sang-Wahn Koo, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
Distinct patterns of <i>de novo</i> coding variants contribute to Tourette Syndrome etiologyLingyu Zhan, Dongmei Yu, Franjo Ivankovic, et al.
Science Translational Medicine|December 13, 2023
DNDI-6174 is a preclinical candidate for visceral leishmaniasis that targets the cytochrome bc<sub>1</sub>Stéphanie Braillard, Martine Keenan, Karen J Breese, et al.
Nature Biomedical Engineering|August 19, 2022
Diagnosis of paediatric tuberculosis by optically detecting two virulence factors on extracellular vesicles in blood samplesWenshu Zheng, Sylvia M LaCourse, Bofan Song, et al.
Nature Genetics|February 11, 2022
GestaltMatcher facilitates rare disease matching using facial phenotype descriptorsTzung-Chien Hsieh, Aviram Bar-Haim, Shahida Moosa, et al.
Nature Genetics|August 7, 2023
PhenoScore quantifies phenotypic variation for rare genetic diseases by combining facial analysis with other clinical features using a machine-learning frameworkAlexander J M Dingemans, Max Hinne, Kim M G Truijen, et al.
American Journal of Human Genetics|December 7, 2015
TAF1 Variants Are Associated with Dysmorphic Features, Intellectual Disability, and Neurological ManifestationsJason A O'Rawe, Yiyang Wu, Max J Dörfel, et al.
Pageof 59