A. R. Mathews

发表

A Novel Frameshift Mutation Causing β-Thalassemia in a Sikh

S. El-kalla, A. R. Mathews, 1995 .

Molecular Characterization of β-Thalassehia in the United Arab Emirates

S. El-kalla, A. R. Mathews, 1993 .

Clinical, cytogenetic & hormonal profile in extreme hypospadias with bilaterally descended testes.

M. Rohatgi, P. Menon, I. Verma, 1986, The Indian journal of medical research.

A Novel β-Thalassemia Mutation [Codon 45 (-T)] in a Pakistani Family

S. El-kalla, A. R. Mathews, 1997 .

A Significant β-Thalassemia Heterogeneity in the United Arab Emirates

S. El-kalla, A. R. Mathews, 1997 .

Hb D-Punjab in the United Arab Emirates.

S. El-kalla, A. R. Mathews, 1997, Hemoglobin.

Analysis of β‐thalassemia mutations in the United Arab Emirates provides evidence for recurrent origin of the IVSINT 5 (G‐C) mutation

A. Novelletto, G. Deidda, L. Felicetti, 1995, Human mutation.

Robinow syndrome (Fetal Face syndrome).

I. Verma, A. Gupta, P. Menon, 1983, Indian pediatrics.

Genetics of ambiguous genitalia

I. Verma, A. R. Mathews, 1982, Indian journal of pediatrics.

del(18p) syndrome with complex tetralogy of Fallot in an infant with 45,X,t(Y;18)(q12;q11.2).

A. R. Mathews, S. el Kalla, N. Menon, 1992, American journal of medical genetics.

Molecular characterization of beta-thalassemia in the United Arab Emirates.

S. El-kalla, A. R. Mathews, 1993, Hemoglobin.

Cytogenetic analysis of down syndrome in Libya

I. Verma, A. El-Zouki, A. R. Mathews, 1990, Indian journal of pediatrics.