Jack Tarleton

A multicenter study on genotype-phenotype correlations in the fragile X syndrome, using direct diagnosis with probe StB12.3: the first 2,253 cases.

François Rousseau, Dominique Heitz, Jack Tarleton et al. · PubMed · 1994 · 294 citations

Characterization of the full fragile X syndrome mutation in fetal gametes

Henry Malter, Jane Iber, Rob Willemsen et al. · Nature Genetics · 1997 · 196 citations

Developmental Anomaly, Developmental Biology, Cytogenetics +10

Evidence of founder chromosomes in fragile X syndrome

Robert I. Richards, Katherine Holman, K. Friend et al. · Nature Genetics · 1992 · 186 citations

Chromatin, Cytogenetics, Genetic Disorder +8

Evidence that methylation of the FMR-I locus is responsible for variable phenotypic expression of the fragile X syndrome.

Allyn McConkie‐Rosell, Ave M. Lachiewicz, Gail A. Spiridigliozzi et al. · PubMed · 1993 · 169 citations

Fragile X syndrome and deletions in FMR1: New case and review of the literature

Lyn S. Hammond, Michelle M. Macias, Jack Tarleton et al. · American Journal of Medical Genetics · 1997 · 145 citations

Full Fmr1 Mutation, Fragile X Syndrome, Fmr1 Gene +13