Author

R Kariminezhad

OpenAlex ID: A5000849760

Molecular Diagnosis in Iranian Patients With Spinal Muscular Atrophy

2004 · Yousef Shafeghati, S H Teymourian, et al. · 7

Short Man With 46,x, Del (yp) Del (yq) Karyotype and More Distal Yq Deletion

2000 · H Najmabad, Y. Shafaghati, et al. · 1

Clinical and Enzymatic Diagnosis of Gm1- Gangliosidosis; a Case Report

2007 · V Shafeghati, G H Vakili, et al.

Beta-thallassemia and Chromosomalaberrations

2002 · M H Kariminezhad, H Najmabad, et al.

Congenital Blindness:report of Leber Congenital Amaurosisin a Large Iranian Kindred

2001 · M H Kariminezhad, Saeed Sohbati, et al.

Epidemiology and Relative Incidence Ofrare Neurometabolic and Neurogeneticdisorders in Iran

2001 · Yousef Shafeghati, R Kariminezhad, et al.

Works count: 6

Citation count: 8

H-index: 1

I10-index: