J. Cohen

A second locus for Rieger syndrome maps to chromosome 13q14.

J. Haines, J. Wiggs, E. D. del Bono, 1996, American journal of human genetics.

HLA-DRB1*15 allele influences the later course of relapsing remitting multiple sclerosis

E. Génin, E. Leray, H. Perdry, 2008, Genes and Immunity.

Expansion and further delineation of the SETD5 phenotype leading to global developmental delay, variable dysmorphic features, and reduced penetrance

A. Serretti, A. Fatemi, K. Gripp, 2018, Clinical genetics.

Reproducibility and complications in gene searches: linkage on chromosome 6, heterogeneity, association, and maternal inheritance in juvenile myoclonic epilepsy.

S Shinnar, S. Moshé, S. Shinnar, 2000, American journal of human genetics.

De novo variants in KLF7 are a potential novel cause of developmental delay/intellectual disability, neuromuscular and psychiatric symptoms

R. Pfundt, T. Kleefstra, C. V. van Ravenswaaij-Arts, 2018, Clinical genetics.

Further evidence that de novo missense and truncating variants in ZBTB18 cause intellectual disability with variable features

W. Chung, A. Fatemi, S. Srivastava, 2017, Clinical Genetics.

Evidence for linkage of adolescent-onset idiopathic generalized epilepsies to chromosome 8-and genetic heterogeneity.

S. Moshé, S. Shinnar, C. Harden, 1999, American journal of human genetics.

No evidence for a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q.

S. Moshé, S. Shinnar, C. Harden, 2000, American journal of medical genetics.