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Publications by Pia Hermanns
TBX15 Mutations Cause Craniofacial Dysmorphism, Hypoplasia of Scapula and Pelvis, and Short Stature in Cousin Syndrome
American Journal of Human Genetics
Genetics
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Dysmorphism-Short Stature-Deafness-Disorder of Sex Development Syndrome
De Novo and Inherited Pathogenic Variants in KDM3B Cause Intellectual Disability, Short Stature, and Facial Dysmorphism
American Journal of Human Genetics
Genetics
ACAN Mutations as a Cause of Familial Short Stature
Clinical Pediatric Endocrinology
Child Health
Endocrinology
Perinatology
Pediatrics
Metabolism
Diabetes
An Unusual Cause of Short Stature-Laron Syndrome
International Journal of Advances in Medicine
Short Stature-Auditory Canal Atresia-Mandibular Hypoplasia-Skeletal Anomalies Syndrome
Mutations in TKT Are the Cause of a Syndrome Including Short Stature, Developmental Delay, and Congenital Heart Defects
American Journal of Human Genetics
Genetics
Choanal Atresia-Hearing Loss-Cardiac Defects-Craniofacial Dysmorphism Syndrome
Dominant-Negative STAT5B Mutations Cause Growth Hormone Insensitivity With Short Stature and Mild Immune Dysregulation
Nature Communications
Astronomy
Genetics
Molecular Biology
Biochemistry
Chemistry
Physics
Short Ulna-Dysmorphism-Hypotonia-Intellectual Disability Syndrome
