Results 101 to 109 of about 323 (109)

The Molecular and Genetic Basis of Fibroblast Growth Factor Receptor 3 Disorders: The Achondroplasia Family of Skeletal Dysplasias, Muenke Craniosynostosis, and Crouzon Syndrome with Acanthosis Nigricans*

Endocrine Reviews, 2000
Zoltan Vajo
exaly  

Growth in achondroplasia: Development of height, weight, head circumference, and body mass index in a European cohort

American Journal of Medical Genetics, Part A, 2018
Giedre Grigelioniene, Outimaija Mäkitie, Klaus Mohnike   +2 more
exaly  

Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia

Cell, 1994
Leslie M Thompson
exaly  

A European tobacco advertising ban

Ca-A Cancer Journal for Clinicians, 1998
exaly  

Commentary on “European Consensus Statement on Lung Cancer”

Ca-A Cancer Journal for Clinicians, 1998
exaly  

European Achondroplasia Forum Practical Considerations for Following Adults with Achondroplasia

Advances in Therapy
Sérgio Sousa, Klaus Mohnike, Encarna Guillén-Navarro   +2 more
exaly  

FAILURE TO DIAGNOSE ACHONDROPLASIA IN UTERO

Lancet, The, 1974
exaly  

Severe pulmonary hypertension in an infant with achondroplasia

Lancet, The, 2001
exaly  

Advances in the management of achondroplasia

Nature Reviews Endocrinology
Ravi Savarirayan
exaly