M. Patel

Linkage analysis identifies an isolated strabismus locus at 14q12 overlapping with FOXG1 syndrome region

Phillip A. Richmond, A. Paterson, C. Ross, 2020, Journal of Medical Genetics.

Mapping one form of autosomal dominant postaxial polydactyly type A to chromosome 7p15-q11.23 by linkage analysis.

U. C. Patel, J. Blouin, U. Radhakrishna, 1997, American journal of human genetics.

A heterozygous truncating mutation in RRM2B causes autosomal-dominant progressive external ophthalmoplegia with multiple mtDNA deletions.

R. Haller, A. Suomalainen, H. Tyynismaa, 2009, American journal of human genetics.

Primate DAX1, SRY, and SOX9: evolutionary stratification of sex-determination pathway.

A. Arnold, J. Sinsheimer, K. Dorman, 2001, American journal of human genetics.

The imprinted region on human chromosome 7q32 extends to the carboxypeptidase A gene cluster: an imprinted candidate for Silver-Russell syndrome

Z Birjandi, L Bentley, K Nakabayashi, 2003, Journal of medical genetics.

Fine mapping of the X‐linked split‐hand/split‐foot malformation (SHFM2) locus to a 5.1‐Mb region on Xq26.3 and analysis of candidate genes

L. Tsui, T. Siddique, W. Ahmad, 2004, Clinical genetics.

Strabismus genetics across a spectrum of eye misalignment disorders

V. Pegado, M. Patel, W. Wasserman, 2014, Clinical genetics.