G. Fouad

Allelic Interaction between CRELD1 and VEGFA in the Pathogenesis of Cardiac Atrioventricular Septal Defects

C. Maslen, E. Feingold, R. Reeves, 2014, AIMS Genetics.

Identification, genomic organization and mRNA expression of CRELD1, the founding member of a unique family of matricellular proteins.

R. Glanville, C. Maslen, S. Robinson, 2002, Gene.

A Randomized, Double-Blind Clinical Study on the Safety and Tolerability of an Iron Multi-Amino Acid Chelate Preparation in Premenopausal Women

Prachi Sharma, M. Evans, N. Guthrie, 2013, Journal of dietary supplements.

A gene for familial paroxysmal dyskinesia (FPD1) maps to chromosome 2q.

E. Bertini, S. Servidei, L. Ptáček, 1996, American journal of human genetics.

Mutations in the human skeletal muscle chloride channel gene (CLCN1) associated with dominant and recessive myotonia congenita

J Zhang, R. Griggs, A. George, 1996, Neurology.

Dihydropyridine receptor mutations cause hypokalemic periodic paralysis

Andrew G. Engel, Robert C. Griggs, Rabi Tawil, 1994, Cell.

Genotype-phenotype correlations of DHP receptor α 1-subunit gene mutations causing hypokalemic periodic paralysis

R. Griggs, J. Mendell, P. Powers, 1997, Neuromuscular Disorders.

Genotype-phenotype correlations of DHP receptor alpha 1-subunit gene mutations causing hypokalemic periodic paralysis.

R. Griggs, J. Mendell, P. Powers, 1997, Neuromuscular disorders : NMD.