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Ben Pode-Shakked

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 24, 2021

Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestationsLance H Rodan, Rebecca C Spillmann, Harley T Kurata, et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 15, 2021

Correction: Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestationsLance H Rodan, Rebecca C Spillmann, Harley T Kurata, et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 18, 2021

DLG4-related synaptopathy: a new rare brain disorderAgustí Rodríguez-Palmero, Melissa Maria Boerrigter, David Gómez-Andrés, et al.

Research Square|June 21, 2024

GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseasesHellen Lesmann, Alexander Hustinx, Shahida Moosa, et al.

Medrxiv : the Preprint Server for Health Sciences|July 28, 2023

GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseasesHellen Lesmann, Alexander Hustinx, Shahida Moosa, et al.

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Search research articles

Showing results (81-90 of 85) with videos related to

Sort By:

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You have reached the last page of results.This site can display upto 85 results.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 24, 2021

Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestationsLance H Rodan, Rebecca C Spillmann, Harley T Kurata, et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 15, 2021

Correction: Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestationsLance H Rodan, Rebecca C Spillmann, Harley T Kurata, et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 18, 2021

DLG4-related synaptopathy: a new rare brain disorderAgustí Rodríguez-Palmero, Melissa Maria Boerrigter, David Gómez-Andrés, et al.

Research Square|June 21, 2024

GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseasesHellen Lesmann, Alexander Hustinx, Shahida Moosa, et al.

Medrxiv : the Preprint Server for Health Sciences|July 28, 2023

GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseasesHellen Lesmann, Alexander Hustinx, Shahida Moosa, et al.

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