S. Leblond

发表

D19S51 is closely linked with and maps distal to the myotonic dystrophy locus on 19q.

G. Shutler, R. Williamson, R. Korneluk, 1991, American journal of human genetics.

Assessment of a creatine kinase isoform M defect as a cause of myotonic dystrophy and the characterization of two novel CKMM polymorphisms

R. Korneluk, A. Mackenzie, S. Leblond, 1991, Human Genetics.

The human ryanodine receptor gene: its mapping to 19q13.1, placement in a chromosome 19 linkage group, and exclusion as the gene causing myotonic dystrophy.

H. Willard, M. Phillips, B. Wieringa, 1990, American journal of human genetics.

RFLP identified by the probe pKE0.6 (D19S117) at human chromosome 19q13.3.

G. Shutler, R. Korneluk, C. Tsilfidis, 1991, Nucleic acids research.

An SstI RFLP detected by the probe pKE2.1 (D19S116) localized to human chromosome 19q13.3.

G. Shutler, R. Korneluk, C. Tsilfidis, 1991, Nucleic acids research.

An insertion polymorphism identified by the probe pE0.8 (D19S115) at 19q13.3.

G. Shutler, R. Korneluk, C. Tsilfidis, 1991, Nucleic acids research.

Physical and genetic mapping of a novel chromosome 19 ERCC1 marker showing close linkage with myotonic dystrophy.

G. Shutler, P. de Jong, B. Wieringa, 1991, Genomics.

Direct haplotyping by double digestion of PCR-amplified creatine kinase (CKMM): application to myotonic dystrophy diagnosis.

C. Junien, R. Korneluk, C. Lavedan, 1990, Genomics.

AvaII RFLP at the human apolipoprotein CII (APO CII) gene locus.

A. Hunter, R. Korneluk, F. Baralle, 1987, Nucleic acids research.