ATR-16 Syndrome: Mechanisms Linking Monosomy to Phenotype

Journal of Medical Genetics - United Kingdom
doi 10.1136/jmedgenet-2019-106528
Full Text
Abstract

Available in full text

Categories
Genetics
Date
Authors
Publisher

BMJ

Related search

Linking Genotype to Clinical Phenotype in Multiple Sclerosis

JAMA Neurology
Neurology
2016English

Ion Channel Mechanisms Related to Sudden Cardiac Death in Phenotype-Negative Long-Qt Syndrome Genotype-Phenotype Correlations of the KCNQ1(S349W) Mutation

Journal of Cardiovascular Electrophysiology
Cardiovascular MedicinePhysiologyCardiology
2010English

Lack of Evidence for Monosomy 1p36 in Patients With Prader-Willi-Like Phenotype

Brazilian Journal of Medical and Biological Research
ImmunologyCell BiologyPharmacologyBiochemistryBiophysicsNeuroscienceMedicineToxicologyPhysiologyPharmaceutics
2008English

Mechanisms Linking Obesity With Male Infertility

Central European Journal of Urology
Urology
2015English

Neuroinflammatory Mechanisms Linking Pain and Depression

Modern Trends in Pharmacopsychiatry
MedicinePsychiatryMental HealthPharmacology
English

The Monosomy 18p Detected by the Amniocentesis: De Grouchy Syndrome 1

Medicinski Casopis
Medicine
2015English

Targeting R-Loop-Associated ATR Response in Myelodysplastic Syndrome

Oncotarget
Oncology
2019English

Monosomy 18p

Orphanet Journal of Rare Diseases
MedicineGeneticsPharmacology
2008English

Ring Chromosome 16 Syndrome

2020English

Amanote Research

Note-taking for researchers

Follow Amanote

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

Privacy PolicyRefund Policy