Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by I-P Chen
Two Novel Large ANKH Deletion Mutations in Sporadic Cases With Craniometaphyseal Dysplasia
Clinical Genetics
Genetics
Related publications
Craniometaphyseal Dysplasia Mutations in ANKH Negatively Affect Human Induced Pluripotent Stem Cell Differentiation Into Osteoclasts
Stem Cell Reports
Biochemistry
Genetics
Developmental Biology
Cell Biology
Craniometaphyseal Dysplasia
Acta Oto-Laryngologica
Medicine
Otorhinolaryngology
Three Novel F8 Mutations in Sporadic Haemophilia a Cases
SpringerPlus
Multidisciplinary
220 Two Cases of Hypohidrotic Ectodermal Dysplasia Caused by Novel Mutations in the EDA Gene
Journal of Investigative Dermatology
Biochemistry
Dermatology
Cell Biology
Molecular Biology
Transcobalamin II Deficiency in Four Cases With Novel Mutations
Turkish Journal of Haematology
Hematology
Two Cases of Maxillary Fibrous Dysplasia
Practica Otologica
Otorhinolaryngology
De Novo Mutations in Sporadic Deletional Duchenne Muscular Dystrophy (DMD) Cases
Experimental & Molecular Medicine
Two Cases of Septo-Optic Dysplasia (SOD)
Endocrine Journal
Endocrinology
Metabolism
Diabetes
Two Cases of Sporadic Late Onset Nemaline Myopathy Effectively Treated With Immunotherapy
Clinical Neurology
Neurology