Genomewide Scan for Hand Osteoarthritis: A Novel Mutation in Matrilin-3

American Journal of Human Genetics - United States
doi 10.1086/375556
Full Text
Abstract

Available in full text

Categories
Genetics
Date
Authors
Publisher

Elsevier BV

Related search

Matrilin-3 Mutations That Cause Chondrodysplasias Interfere With Protein Trafficking While a Mutation Associated With Hand Osteoarthritis Does Not

Journal of Medical Genetics
Genetics
2005English

Spondylo-Epi-Metaphyseal Dysplasia (SEMD) Matrilin 3 Type: Homozygote Matrilin 3 Mutation in a Novel Form of SEMD

Journal of Medical Genetics
Genetics
2004English

A Genomewide Scan for Loci Involved in Attention-Deficit/Hyperactivity Disorder

American Journal of Human Genetics
Genetics
2002English

A Genomewide Linkage Scan for Quantitative-Trait Loci for Obesity Phenotypes

American Journal of Human Genetics
Genetics
2002English

Genomewide Scan for Real-Word Reading Subphenotypes of Dyslexia: Novel Chromosome 13 Locus and Genetic Complexity

American Journal of Medical Genetics, Part B, Neuropsychiatric Genetics
PsychiatryMolecular NeuroscienceMental HealthGeneticsCellular
2006English

Spondyloepimetaphyseal Dysplasia, Matrilin-3 Type

2020English

Expanded Genomewide Scan Implicates a Novel Locus at 3q28 Among Caribbean Hispanics With Familial Alzheimer Disease

Archives of Neurology
2006English

New Guidelines for Hand Osteoarthritis

BMJ
2007English

A Genomewide Scan for Attention-Deficit/Hyperactivity Disorder in an Extended Sample: Suggestive Linkage on 17p11

American Journal of Human Genetics
Genetics
2003English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy