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Publications by Ester Sallicandro
Report of a Novel SHOX Missense Variant in a Boy With Short Stature and His Mother With Leri–Weill Dyschondrosteosis
Frontiers in Endocrinology
Endocrinology
Metabolism
Diabetes
Related publications
Impairment of SHOX Nuclear Localization as a Cause for Leri-Weill Syndrome
Journal of Cell Science
Cell Biology
Identification of a Major Recombination Hotspot in Patients With Short Stature and SHOX Deficiency
American Journal of Human Genetics
Genetics
Investigation of SHOX Gene Mutations in Turkish Patients With Idiopathic Short Stature
JCRPE Journal of Clinical Research in Pediatric Endocrinology
Child Health
Endocrinology
Perinatology
Pediatrics
Metabolism
Diabetes
Discondrosteosis De Leri-Weill
Revista Chilena de Pediatria
Child Health
Pediatrics
Perinatology
An Intragenic Deletion Within CTNNA2 Intron 7 in a Boy With Short Stature and Speech Delay: A Case Report
SAGE Open Medical Case Reports
Detection of SHOX Gene Variations in Patients Who Had Skeletal Abnormalities With/Without Short Stature
JCRPE Journal of Clinical Research in Pediatric Endocrinology
Child Health
Endocrinology
Perinatology
Pediatrics
Metabolism
Diabetes
Comparison of Methods for Final Height Assessment in Adolescents With a Normal Variant Short Stature
Journal of Human Growth and Development
Life-course Studies
Life-span
New PCNT Candidate Missense Variant in a Patient With Oral and Maxillofacial Osteodysplasia: A Case Report
BMC Medical Genetics
Genetics
Radius Wedge Osteotomy in Madelung Deformity of Leri-Weill Syndrome.
Orthopedics & Traumatology