Identification of Eight Novel VEGFR-3 Mutations in Families With Primary Congenital Lymphoedema

Journal of Medical Genetics - United Kingdom
doi 10.1136/jmg.40.9.697
Full Text
Abstract

Available in full text

Categories
Genetics
Date
Authors
Publisher

BMJ

Related search

Novel Mutations in CRYGC Are Associated With Congenital Cataracts in Chinese Families

Scientific Reports
Multidisciplinary
2017English

Identification of Three ADA2 Deficiency Families With Novel CECR1 Mutations

Pediatric Rheumatology
ImmunologyPediatricsRheumatologyAllergyPerinatologyChild Health
2015English

Identification of Novel LEPR Mutations in Pakistani Families With Morbid Childhood Obesity

BMC Medical Genetics
Genetics
2018English

A Spectrum of CYP1B1 Mutations Associated With Primary Congenital Glaucoma in Families of Pakistani Descent

Human Genome Variation
BiochemistryGeneticsMolecular Biology
2016English

Congenital Hereditary Lymphoedema

Journal of Medical Genetics
Genetics
1965English

Identification of Two Novel LAMA2 Mutations in a Chinese Patient With Congenital Muscular Dystrophy

Frontiers in Genetics
GeneticsMolecular Medicine
2018English

Identification and in Silico Analysis of GALNS Mutations Causing Morquio a Syndrome in Eight Consanguineous Families

Turkish Journal of Biology
GeneticsCell BiologyMolecular BiologyMicrobiologyBiological SciencesAgriculturalPhysiology
2017English

Novel Mutations of TMPRSS3 in Four DFNB8/B10 Families Segregating Congenital Autosomal Recessive Deafness

Journal of Medical Genetics
Genetics
2001English

Targeted Regions Sequencing Identified Four Novel PNPLA1 Mutations in Two Chinese Families With Autosomal Recessive Congenital Ichthyosis

Molecular genetics & genomic medicine
GeneticsMolecular Biology
2019English

Amanote Research

Note-taking for researchers

Follow Amanote

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

Privacy PolicyRefund Policy