Tb(III)-ion-binding-induced conformational changes in platelet factor XIII.

Por Achyuthan, K E, Mary, A, Greenberg, C S
Publicado em 1989

Interstitial deletion of the short arm of chromosome 4.

Por Ray, M, Evans, J, Rockman-Greenberg, C, Wickstrom, D
Publicado em 1984

DNA studies in a family with Duchenne muscular dystrophy and a deletion at Xp21.

Por Greenberg, C R, Hamerton, J L, Nigli, M, Wrogemann, K
Publicado em 1987

A rare case of Niemann–Pick disease type C without neurological involvement in a 66-year-old patient

Por Greenberg, C.R., Barnes, J.G., Kogan, S., Seargeant, L.E.
Publicado no Mol Genet Metab Rep (2015)

Cleavage of blood coagulation factor XIII and fibrinogen by thrombin during in vitro clotting.

Por Greenberg, C S, Miraglia, C C, Rickles, F R, Shuman, M A
Publicado em 1985

Subregional assignment of the linked marker G8 (D4S10) for Huntington disease to chromosome 4p16.1-16.3.

Por Wang, H S, Greenberg, C R, Hewitt, J, Kalousek, D, Hayden, M R
Publicado em 1986

Localization of the gene for coagulation factor XIII a-chain to chromosome 6 and identification of sites of synthesis.

Por Weisberg, L J, Shiu, D T, Greenberg, C S, Kan, Y W, Shuman, M A
Publicado em 1987

Isolation of a fibrin-binding fragment from blood coagulation factor XIII capable of cross-linking fibrin(ogen).

Por Greenberg, C S, Enghild, J J, Mary, A, Dobson, J V, Achyuthan, K E
Publicado em 1988

Reversible renal resistance to aldosterone associated with interstitial nephritis.

Por Regan, J J, Greenberg, C S, Mooradian, A D, Staley, N, Nuttall, F Q
Publicado em 1987

Hyperphosphatemia in infantile hypophosphatasia: implications for carrier diagnosis and screening.

Por Chodirker, B N, Evans, J A, Seargeant, L E, Cheang, M S, Greenberg, C R
Publicado em 1990

Limb-girdle muscular dystrophy and Miyoshi myopathy in an aboriginal Canadian kindred map to LGMD2B and segregate with the same haplotype.

Por Weiler, T., Greenberg, C. R., Nylen, E., Halliday, W., Morgan, K., Eggertson, D., Wrogemann, K.
Publicado em 1996

Effects of a low-fat high-carbohydrate diet on plasma sex hormones in premenopausal women: results from a randomized controlled trial. Canadian Diet and Breast Cancer Prevention St...

Por Boyd, N. F., Lockwood, G. A., Greenberg, C. V., Martin, L. J., Tritchler, D. L.
Publicado em 1997

Successful therapy for protein-losing enteropathy caused by chronic neuronopathic Gaucher disease

Por Mhanni, A.A., Kozenko, M., Hartley, J.N., Deneau, M., El-Matary, W., Rockman-Greenberg, C.
Publicado no Mol Genet Metab Rep (2015)

Retrospective TREC testing of newborns with Severe Combined Immunodeficiency and other primary immunodeficiency diseases

Por Jilkina, O., Thompson, J.R., Kwan, L., Van Caeseele, P., Rockman-Greenberg, C., Schroeder, M.L.
Publicado no Mol Genet Metab Rep (2014)

Impact of genetic counselling after neonatal screening for Duchenne muscular dystrophy.

Por Hildes, E, Jacobs, H K, Cameron, A, Seshia, S S, Booth, F, Evans, J A, Wrogemann, K, Greenberg, C R
Publicado em 1993

A gene for autosomal recessive limb-girdle muscular dystrophy in Manitoba Hutterites maps to chromosome region 9q31-q33: evidence for another limb-girdle muscular dystrophy locus.

Por Weiler, T, Greenberg, C R, Zelinski, T, Nylen, E, Coghlan, G, Crumley, M J, Fujiwara, T M, Morgan, K, Wrogemann, K
Publicado em 1998

Infantile hypophosphatasia: localization within chromosome region 1p36.1-34 and prenatal diagnosis using linked DNA markers.

Por Greenberg, C R, Evans, J A, McKendry-Smith, S, Redekopp, S, Haworth, J C, Mulivor, R, Chodirker, B N
Publicado em 1990

Exclusion of the gelsolin gene on 9q32-34 as the cause of familial lattice corneal dystrophy type I.

Por Wiens, A, Marles, S, Safneck, J, Kwiatkowski, D J, Maury, C P, Zelinski, T, Philipps, S, Ekins, M B, Greenberg, C R
Publicado em 1992

Molecular characterization of the marker chromosome associated with cat eye syndrome.

Por Mears, A. J., Duncan, A. M., Budarf, M. L., Emanuel, B. S., Sellinger, B., Siegel-Bartelt, J., Greenberg, C. R., McDermid, H. E.
Publicado em 1994

Congenital hydrocephalus secondary to Walker-Warburg syndrome identified on the Manitoba Neonatal Screening Programme for Duchenne muscular dystrophy.

Por Greenberg, C R, Jacobs, H K, Nylen, T E, Gibb, M, Chodirker, B N, Moffatt, M, Lacson, A, Halliday, W, Bernier, F, el-Husseini, A
Publicado em 1992