Related Experiment Videos
In memory of Murray Feingold (1930-2015)
G Bradley Schaefer1, Catherine Bearce Nowak2, Ann Haskins Olney3
1University of Arkansas for Medical Sciences, Arkansas Children's Hospital, Little Rock, Arkansas.
American Journal of Medical Genetics. Part A
|May 6, 2016
Summary
No abstract available in PubMed .
Related Concept Videos
You might also read
Related Articles
Articles linked to this work by shared authors, journal, and citation graph.
Sort by
Same author
Pathogenic XPO1 variants cause a dominant neurodevelopmental disorder.
Genetics in medicine : official journal of the American College of Medical Genetics·2025
Same author
Transmembrane protein 53 craniotubular dysplasia (OMIM # 619727): The skeletal disease and consequent blindness of this new disorder.
Bone·2024
Same author
Correction: Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals.
European journal of human genetics : EJHG·2024
Same author
TRIM71 mutations cause a neurodevelopmental syndrome featuring ventriculomegaly and hydrocephalus.
Brain : a journal of neurology·2024
Same author
Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals.
European journal of human genetics : EJHG·2024
Same author
Bi-allelic variants in INTS11 are associated with a complex neurological disorder.
American journal of human genetics·2023
Same journal
How does Léri-Weill Dyschondrosteosis Affect Adults' Health-Related Quality of Life? - A Norwegian Cross-Sectional Study Exploring the Physical and Mental Burden.
American journal of medical genetics. Part A·2026
Same journal
Re-Identification of the Panamanian Guna/Kuna/Cuna OCA2 Founder Association Through Two American-Born Siblings.
American journal of medical genetics. Part A·2026
Same journal
Biallelic Variant in HAPLN1 is Associated With Skeletal Dysplasia With or Without Congenital Heart Disease.
American journal of medical genetics. Part A·2026
Same journal
MYH11-Related Hereditary Type 2 Visceral Myopathy in a Large Kindred: Diagnostic Odyssey With Milder Clinical Manifestations.
American journal of medical genetics. Part A·2026
Same journal
Positron Emission Tomography (PET) in Phenylketonuria: A Systematic Review of Brain Metabolism Beyond Phenylalanine.
American journal of medical genetics. Part A·2026
Same journal
Re: "Clinical Insights From a Case of Sifrim-Hitz-Weiss Syndrome With a CHD4 Variant: Expanding the Phenotypic Spectrum and Its Response to Growth Hormone Therapy".
American journal of medical genetics. Part A·2026