Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by Parag M Tamhankar
Identification of Novel ROR2 Gene Mutations in Indian Children With Robinow Syndrome
JCRPE Journal of Clinical Research in Pediatric Endocrinology
Child Health
Endocrinology
Perinatology
Pediatrics
Metabolism
Diabetes
Related publications
Reply to Mazzeu: Human Mutations inRYKMight Cause Robinow Syndrome
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Pesquisa De Mutações No Gene ROR2 Em Pacientes Com a Forma Recessiva Da Síndrome De Robinow
Vitamin D Receptor Gene Polymorphisms in Indian Children With Idiopathic Nephrotic Syndrome
International Journal of Human Genetics
Genetics
Autosomal Dominant Robinow Syndrome
Gray Platelet Syndrome: Novel Mutations of the NBEAL2 Gene
American Journal of Hematology
Hematology
Usher Syndrome Type III: Revised Genomic Structure of the USH3 Gene and Identification of Novel Mutations
American Journal of Human Genetics
Genetics
Novel Mutations in the IRF6 Gene in Brazilian Families With Van Der Woude Syndrome
International Journal of Molecular Medicine
Medicine
Genetics
Novel GRN Mutations in Patients With Corticobasal Syndrome
Scientific Reports
Multidisciplinary
Identification of Novel Mutations in the HbF Repressor Gene BCL11A in Patients With Autism and Intelligence Disabilities
American Journal of Hematology
Hematology
