A radio-ligand receptor assay for the long-acting thyroid stimulator. Inhibition by the long-acting thyroid stimulator of the binding of radioiodinated thyroid-stimulating hormone...

Por Mehdi, S Q, Nussey, S S
Publicado em 1975

Identification of novel mutations in the SEMA4A gene associated with retinal degenerative diseases

Por Abid, A, Ismail, M, Mehdi, S Q
Publicado em 2006

Allogeneic cytolysis of reconstituted membrane vesicles.

Por Hollander, N, Mehdi, S Q, Weissman, I L, McConnell, H M, Kriss, J P
Publicado em 1979

A locus for autosomal recessive congenital microphthalmia maps to chromosome 14q32.

Por Bessant, D A, Khaliq, S, Hameed, A, Anwar, K, Mehdi, S Q, Payne, A M, Bhattacharya, S S
Publicado em 1998

Refinement of the locus for autosomal recessive Retinitis pigmentosa (RP25) linked to chromosome 6q in a family of Pakistani origin.

Por Khaliq, S, Hameed, A, Ismail, M, Mehdi, S Q, Bessant, D A, Payne, A M, Bhattacharya, S S
Publicado em 1999

A Novel ABCA12 Mutation in Two Families with Congenital Ichthyosis

Por Walsh, D. M., Shah, S. H., Simpson, M. A., Morgan, N. V., Khaliq, S., Trembath, R. C., Mehdi, S. Q., Maher, E. R.
Publicado em 2012

Polarity and Temporality of High-Resolution Y-Chromosome Distributions in India Identify Both Indigenous and Exogenous Expansions and Reveal Minor Genetic Influence of Central Asia...

Por Sengupta, Sanghamitra, Zhivotovsky, Lev A., King, Roy, Mehdi, S. Q., Edmonds, Christopher A., Chow, Cheryl-Emiliane T., Lin, Alice A., Mitra, Mitashree, Sil, Samir K., Ramesh, A., Usha Rani, M. V., Thakur, Chitra M., Cavalli-Sforza, L. Luca, Majumder, Partha P., Underhill, Peter A.
Publicado em 2006

Dynamin 2 homozygous mutation in humans with a lethal congenital syndrome

Por Koutsopoulos, Olga S, Kretz, Christine, Weller, Claudia M, Roux, Aurelien, Mojzisova, Halina, Böhm, Johann, Koch, Catherine, Toussaint, Anne, Heckel, Emilie, Stemkens, Daphne, ter Horst, Simone A J, Thibault, Christelle, Koch, Muriel, Mehdi, Syed Q, Bijlsma, Emilia K, Mandel, Jean-Louis, Vermot, Julien, Laporte, Jocelyn
Publicado em 2013

Differential structuring of human populations for homologous X and Y microsatellite loci.

Por Scozzari, R, Cruciani, F, Malaspina, P, Santolamazza, P, Ciminelli, B M, Torroni, A, Modiano, D, Wallace, D C, Kidd, K K, Olckers, A, Moral, P, Terrenato, L, Akar, N, Qamar, R, Mansoor, A, Mehdi, S Q, Meloni, G, Vona, G, Cole, D E, Cai, W, Novelletto, A
Publicado em 1997

Network analyses of Y-chromosomal types in Europe, northern Africa, and western Asia reveal specific patterns of geographic distribution.

Por Malaspina, P, Cruciani, F, Ciminelli, B M, Terrenato, L, Santolamazza, P, Alonso, A, Banyko, J, Brdicka, R, García, O, Gaudiano, C, Guanti, G, Kidd, K K, Lavinha, J, Avila, M, Mandich, P, Moral, P, Qamar, R, Mehdi, S Q, Ragusa, A, Stefanescu, G, Caraghin, M, Tyler-Smith, C, Scozzari, R, Novelletto, A
Publicado em 1998