Article

H63D-Syndrome: Quick Reference Guide

2021-12-16

Abstract excerpt

Herewith the most condensed and at the same time most comprehensible guide to Gene H63D Syndrome is available. It is specifically made for general physicians in primary and family medicine.

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: 4a461b6d-41af-576b-ac23-b46441feb654
DOI: 10.22541/au.163967137.78856688/v1

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

H63D-Syndrome: Quick Reference GuideDOI 10.22541/au.163967137.78856688/v1Read

How to diagnose H63D Syndrome Type-2Semantic proximity Read

Human Gene Mutation Database (HGMD): 2003 update.Semantic proximity Read

H63D Syndrome: A rare clinical phenotype caused by a homozygous mutation of HFE gene H63DSemantic proximity Read

NIMH Human Genetics Initiative: 2003 update.Semantic proximity Read

In this issue: defined patient populations are required to establish genetic pathogenesis.Semantic proximity Read

Nomenclature for human DPYD alleles.Semantic proximity Read

H63D Mutation Syndrome Type-2Semantic proximity Read

Clinical utility gene card for: 3-M syndrome - update 2013.Semantic proximity Read

Nomenclature for the description of human sequence variations.Semantic proximity Read

Clinical utility gene card for: Alport syndrome - update 2014.Semantic proximity Read

Precision Medicine for Continuing Phenotype Expansion of Human Genetic Diseases.Semantic proximity Read

Oshtoran Syndrome (H63D Syndrome Type-3)Semantic proximity Read