J. Spranger

Discipline

Anthropologie biologique (3)

Type de document

Articles (6) Recensions (1)

Co-auteur

Date

Source

Mot-clé

Genes (5) association (4) Social groups (4) Human beings (4) roman (4) risque (3) gène (3) maladie (3) Development (3) Diseases (3) Cases (3) Risk (3) Non-insulin-dependent diabetes (3) Meta-analysis (3) Diseases (3) Disease susceptibility (3) Diabetes (3) Cases (3) maladie (3) biologie (2) protéine (2) analyse (2) génétique (2) adulte (2) Diagnosis (2) Genetics (2) Patients (2) Insulin resistance (2) Insulin (2) Homeostasis (2)

Documents écrit par J. Spranger (6) | parle de J. Spranger (0)

Hypomorphic mutations of TRIP11 cause odontochondrodysplasia.
A. Wehrle et al. (7 févr. 2019)
Pseudoachondroplasia and multiple epiphyseal dysplasia: a 7-year comprehensive analysis of the known disease genes identify novel and recurrent mutations and provides an accurate assessment of their relative contribution.
G.C. Jackson et al. (2012)
A genome-wide association search for type 2 diabetes genes in African Americans.
N.D. Palmer et al. (2012)
Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.
Z. Dastani et al. (2012)
Nosology and classification of genetic skeletal disorders: 2010 revision.
M.L. Warman et al. (2011)
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.
J. Dupuis et al.