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M Pierson

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The American Journal of Surgical Pathology|March 7, 2024

The Spectrum of Non-neoplastic Changes Associated With Breast Implants: Histopathology, Imaging, and Clinical SignificanceMario L Marques-Piubelli, Kirill A Lyapichev, Aakash Fnu, et al.

Human Mutation|July 17, 2013

Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation in C19orf12Guida Landouré, Peng-Peng Zhu, Charles M Lourenço, et al.

Pediatric Neurology|May 25, 2020

Epilepsy and Electroencephalographic Abnormalities in SATB2-Associated SyndromeHannah Lewis, Debopam Samanta, Jenny-Li Örsell, et al.

American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|November 14, 2019

The CHD8 overgrowth syndrome: A detailed evaluation of an emerging overgrowth phenotype in 27 patientsPhilip J Ostrowski, Anna Zachariou, Chey Loveday, et al.

Brain Communications|July 9, 2021

International retrospective natural history study of <i>LMNA</i>-related congenital muscular dystrophyRabah Ben Yaou, Pomi Yun, Ivana Dabaj, et al.

Human Mutation|March 1, 2019

SLC35A2-CDG: Functional characterization, expanded molecular, clinical, and biochemical phenotypes of 30 unreported IndividualsBobby G Ng, Paulina Sosicka, Satish Agadi, et al.

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Search research articles

Showing results (221-230 of 226) with videos related to

Sort By:

Pageof 23

You have reached the last page of results.This site can display upto 226 results.

The American Journal of Surgical Pathology|March 7, 2024

The Spectrum of Non-neoplastic Changes Associated With Breast Implants: Histopathology, Imaging, and Clinical SignificanceMario L Marques-Piubelli, Kirill A Lyapichev, Aakash Fnu, et al.

Human Mutation|July 17, 2013

Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation in C19orf12Guida Landouré, Peng-Peng Zhu, Charles M Lourenço, et al.

Pediatric Neurology|May 25, 2020

Epilepsy and Electroencephalographic Abnormalities in SATB2-Associated SyndromeHannah Lewis, Debopam Samanta, Jenny-Li Örsell, et al.

American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|November 14, 2019

The CHD8 overgrowth syndrome: A detailed evaluation of an emerging overgrowth phenotype in 27 patientsPhilip J Ostrowski, Anna Zachariou, Chey Loveday, et al.

Brain Communications|July 9, 2021

International retrospective natural history study of <i>LMNA</i>-related congenital muscular dystrophyRabah Ben Yaou, Pomi Yun, Ivana Dabaj, et al.

Human Mutation|March 1, 2019

SLC35A2-CDG: Functional characterization, expanded molecular, clinical, and biochemical phenotypes of 30 unreported IndividualsBobby G Ng, Paulina Sosicka, Satish Agadi, et al.

Pageof 23