Management of hyperphenylalaninaemia (HPA) in Northern Ireland.

Autor Carson, N A
Vydáno 1971

Diagnosis and management of hyperphenylalaninaemia.

Autor Carson, N A
Vydáno 1971

Homocystinuria.

Autor Carson, N. A.
Vydáno 1970

Biochemical response to oral pyridoxine in homocystinuria.

Autor Carson, N. A.
Vydáno 1968

Two HinfI RFLPs detected by p alpha 10RP8 at D10Z1.

Autor Carson, N L, Simpson, N E
Vydáno 1990

Cystathionase deficiency in fibroblast cultures from a patient with primary cystathioninuria.

Autor Bittles, A H, Carson, N A
Vydáno 1974

Treatment of homocystinuria with pyridoxine. A preliminary study.

Autor Carson, N. A., Carré, I. J.
Vydáno 1969

Severe mental retardation due to maternal phenylketonuria.

Autor Nevin, N. C., Carson, N. A.
Vydáno 1982

A PvuII RFLP detected by pOB231 at CDC2 on human chromosome 10

Autor Carson, N.L., Myers, S., Simpson, N.E.
Vydáno 1991

Molecular screening for Smith-Magenis syndrome among patients with mental retardation of unknown cause

Autor Struthers, J, Carson, N, McGill, M, Khalifa, M
Vydáno 2002

Results of routine screening for phenylketonuria in early infancy, Northern Ireland (1960-67).

Autor Carson, N. A., Carré, I. J., Neill, D. W.
Vydáno 1968

Prolonged Bleeding-time and A.H.G. Deficiency

Autor Carré, I. J., Campbell, S., Nicholi, B., Carson, N. A. J.
Vydáno 1961

Congenital ophthalmoplegia, floppy baby syndrome, myopathy, and aminoaciduria. Report of a family.

Autor Hurwitz, L J, Carson, N A, Allen, I V, Chopra, J S
Vydáno 1969

Hereditary tyrosinaemia. Clinical, enzymatic, and pathological study of an infant with the acute form of the disease.

Autor Carson, N A, Biggart, J D, Bittles, A H, Donovan, D
Vydáno 1976

The mutation for medullary thyroid carcinoma with parathyroid tumors (MTC with PTs) is closely linked to the centromeric region of chromosome 10.

Autor Carson, N L, Wu, J S, Jackson, C E, Kidd, K K, Simpson, N E
Vydáno 1990

Ovarian failure in a young woman with galactosaemia.

Autor Morrow, R. J., Atkinson, A. B., Carson, D. J., Carson, N. A., Sloan, J. M., Traub, A. I.
Vydáno 1985

GW3965, a synthetic liver X receptor (LXR) agonist, reduces angiotensin II-mediated pressor responses in Sprague–Dawley rats

Autor Leik, C E, Carson, N L, Hennan, J K, Basso, M D, Liu, Q-Y, Crandall, D L, Nambi, P
Vydáno 2007

Individual and family characteristics associated with protein truncating BRCA1 and BRCA2 mutations in an Ontario population based series from the Cooperative Family Registry for Br...

Autor Ozcelik, H, Knight, J, Glendon, G, Yazici, H, Carson, N, Ainsworth, P, Taylor, S, Feilotter, H, Carter, R, Boyd, N, Andrulis, I
Vydáno 2003

Paenibacillus larvae Phage Tripp Genome Has 378-Base-Pair Terminal Repeats

Autor Abraham, J., Bousquet, A.-C., Bruff, E., Carson, N., Clark, A., Connell, A., Davis, Z., Dums, J., Everington, C., Groth, A., Hawes, N., McArthur, N., McKenney, C., Oufkir, A., Pearce, B., Rampal, S., Rozier, H., Schaff, J., Slehria, T., Carson, S., Miller, E. S.
Vydáno v Genome Announc (2016)

Proceed with Care: Direct Predictive Testing for Huntington Disease

Autor Benjamin, C. M., Adam, S., Wiggins, S., Theilmann, J. L., Copley, T. T., Bloch, M., Squitieri, F., McKellin, W., Cox, S., Brown, S. A., Kremer, H. P. H., Burgess, M., Meshino, W., Summers, A., Macgregor, D., Buchanan, J., Greenberg, C., Carson, N., Ives, E., Frecker, M., Welch, J. P., Fuller, A., Rosenblatt, D., Miller, S., Dufrasne, S., Roy, M., Andermann, E., Prevost, C., Khalifa, M., Girard, K., Taylor, S., Hunter, A., Goldsmith, C., Whelan, D., Eisenberg, D., Soltan, H., Kane, J., Shokeir, M. H. K., Gibson, A., Cardwell, S., Bamforth, S., Grover, S., Suchowersky, O., Klimek, M., Garber, T., Gardner, H. A., MacLeod, P., Hayden, M. R.
Vydáno 1994