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발행년	- (예 : 2010-2015)

Molecular analysis and clinical correlations of the Huntington's disease mutation.

Academic Journal

Lancet. 10/16/93, Vol. 342 Issue 8877, p954. 5p. 2 Black and White Photographs, 1 Diagram, 2 Charts, 4 Graphs.

Full Text (ScienceDirect 종량제) Full Text (ProQuest Central) Web of Science JCR 저널정보 Scopus Find it@PNU

Widespread prevalence of a CREBRF variant amongst Māori and Pacific children is associated with weight and height in early childhood

Periodical

Berry, S D; Walker, C G; Ly, K; Snell, R G; Atatoa Carr, P E; Bandara, D; Mohal, J; Castro, T G; Marks, E J; Morton, S M B; Grant, C C

International Journal of Obesity (formerly International Journal of Obesity and Related Metabolic Disorders); April 2018, Vol. 42 Issue: 4 p603-607, 5p

Full Text (ProQuest Central) Full Text (Gale Academic Onefile) Open Access (EBSCO) Web of Science JCR 저널정보 Scopus Find it@PNU

Widespread prevalence of a CREBRF variant amongst M[a macro]ori and Pacific children is associated with weight and height in early childhood

Academic Journal

Berry, S D; Walker, C G; Ly, K; Snell, R G; Atatoa Carr, P E; Bandara, D; Mohal, J; Castro, T G; Marks, E J; Morton, S M B; Grant, C C

International Journal of Obesity. April, 2018, Vol. 42 Issue 4, p603

Full Text (ProQuest Central) Full Text (Gale Academic Onefile) Open Access (EBSCO) Web of Science JCR 저널정보 Scopus Find it@PNU

Late-onset Huntington's disease: a clinical and molecular study.

Academic Journal

James, C M; Houlihan, G D; Snell, R G; Cheadle, J P; Harper, P S

Age & Ageing. Nov94, Vol. 23 Issue 6, p445-448. 4p.

Full Text (Gale General Onefile) Full Text (Gale Academic Onefile) Web of Science JCR 저널정보 Scopus Find it@PNU

Paternal origin of the chromosomal deletion resulting in Wolf-Hirschhorn syndrome.

Academic Journal

Quarrell, O W; Snell, R G; Curtis, M A; Roberts, S H; Harper, P S; Shaw, D J

Journal of Medical Genetics; Apr1991, Vol. 28 Issue 4, p256-259, 4p, 1 Black and White Photograph, 1 Diagram, 2 Charts

Full Text (BMJ Journals) Web of Science JCR 저널정보 Scopus Find it@PNU

Linkage disequilibrium and recombination make a telomeric site for the Huntington's disease gene unlikely.

Academic Journal

Barron, L; Curtis, A; Shrimpton, A E; Holloway, S; May, H; Snell, R G; Brock, D J

Journal of Medical Genetics; Aug1991, Vol. 28 Issue 8, p520-522, 3p, 1 Diagram, 1 Chart

Full Text (BMJ Journals) Web of Science JCR 저널정보 Scopus Find it@PNU

Linkage disequilibrium in Huntington's disease: an improved localisation for the gene.

Academic Journal

Snell, R G; Lazarou, L P; Youngman, S; Quarrell, O W; Wasmuth, J J; Shaw, D J; Harper, P S

Journal of Medical Genetics; Nov1989, Vol. 26 Issue 11, p673-675, 3p, 1 Chart

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Identification of an expanded CAG repeat in the Huntington's disease gene (IT15) in a family reported to have benign hereditary chorea.

Academic Journal

MacMillan, J C; Morrison, P J; Nevin, N C; Shaw, D J; Harper, P S; Quarrell, O W; Snell, R G

Journal of Medical Genetics; Dec1993, Vol. 30 Issue 12, p1012-1013, 2p, 1 Black and White Photograph, 1 Diagram

Full Text (BMJ Journals) Web of Science JCR 저널정보 Scopus Find it@PNU

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