C. Meredith

发表

Early onset chromosome 14-linked distal myopathy (Laing)

F. Mastaglia, L. Cala, N. Laing, 2002, Neuromuscular Disorders.

Autosomal dominant distal myopathy: linkage to chromosome 14.

F. Mastaglia, N. Laing, P. Robbins, 1995, American journal of human genetics.

Assignment of the human slow skeletal muscle troponin gene (TNNI1) to 1q32 by fluorescence in situ hybridisation.

L. Kedes, N. Laing, H. Eyre, 1993, Cytogenetics and cell genetics.

Mutations in the slow skeletal muscle fiber myosin heavy chain gene (MYH7) cause laing early-onset distal myopathy (MPD1).

F. Mastaglia, P. Hedera, N. Laing, 2004, American journal of human genetics.

Molecular genetic investigation of autosomal dominant muscular dystrophy

C. Meredith, 2001 .

Autosomal dominant distal myopathy not linked to the known distal myopathy loci

J. Hallmayer, N. Laing, K. Felice, 1999, Neuromuscular Disorders.

Assignment of the human beta tropomyosin gene (TPM2) to band 9p13 by fluorescence in situ hybridisation.

N. Laing, D. Callen, S. Wilton, 1995, Cytogenetics and cell genetics.

Assignment of the human skeletal muscle alpha actin gene (ACTA1) to 1q42 by fluorescence in situ hybridisation.

L. Kedes, N. Laing, D. Callen, 1994, Cytogenetics and cell genetics.

Uva-dare (digital Academic Repository) Mutations in the Slow Skeletal Muscle Fiber Myosin Heavy Chain Gene (myh7) Cause Laing Early-onset Distal Myopathy (mpd1)

F. Mastaglia, P. Hedera, N. Laing, 2022 .