S Kelly

Cell division and cell allocation in early mouse development

S Kelly, Jacques Mulnard, Christopher F. Graham · Development · 1978 · 156 citations

Novel splicing, missense, and deletion mutations in seven adenosine deaminase-deficient patients with late/delayed onset of combined immunodeficiency disease. Contribution of genotype to phenotype.

Inés Santisteban, F X Arredondo-Vega, S Kelly et al. · Journal of Clinical Investigation · 1993 · 100 citations · Full text

Active Ada, Genetics, Immunodeficiencies +17

Three new adenosine deaminase mutations that define a splicing enhancer and cause severe and partial phenotypes: implications for evolution of a CpG hotspot and expression of a transduced ADA cDNA

Inés Santisteban, F X Arredondo-Vega, S Kelly et al. · Human Molecular Genetics · 1995 · 61 citations

Sustained remission of severe resistant autoimmune neutropenia with Campath‐1H

Sally Killick, Judith Marsh, G Hale et al. · British Journal of Haematology · 1997 · 42 citations · Full text

Correct splicing despite mutation of the invariant first nucleotide of a 5' splice site: a possible basis for disparate clinical phenotypes in siblings with adenosine deaminase deficiency.

F X Arredondo-Vega, Inés Santisteban, S Kelly et al. · PubMed · 1994 · 39 citations