Management of hyperphenylalaninaemia (HPA) in Northern Ireland.

od Carson, N A
Izdano 1971

Diagnosis and management of hyperphenylalaninaemia.

od Carson, N A
Izdano 1971

Homocystinuria.

od Carson, N. A.
Izdano 1970

Biochemical response to oral pyridoxine in homocystinuria.

od Carson, N. A.
Izdano 1968

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

od Carson, N L, Simpson, N E
Izdano 1990

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

od Bittles, A H, Carson, N A
Izdano 1974

Treatment of homocystinuria with pyridoxine. A preliminary study.

od Carson, N. A., Carré, I. J.
Izdano 1969

Severe mental retardation due to maternal phenylketonuria.

od Nevin, N. C., Carson, N. A.
Izdano 1982

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

od Carson, N.L., Myers, S., Simpson, N.E.
Izdano 1991

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

od Struthers, J, Carson, N, McGill, M, Khalifa, M
Izdano 2002

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

od Carson, N. A., Carré, I. J., Neill, D. W.
Izdano 1968

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

od Carré, I. J., Campbell, S., Nicholi, B., Carson, N. A. J.
Izdano 1961

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

od Hurwitz, L J, Carson, N A, Allen, I V, Chopra, J S
Izdano 1969

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

od Carson, N A, Biggart, J D, Bittles, A H, Donovan, D
Izdano 1976

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

od Carson, N L, Wu, J S, Jackson, C E, Kidd, K K, Simpson, N E
Izdano 1990

Ovarian failure in a young woman with galactosaemia.

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

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

od Leik, C E, Carson, N L, Hennan, J K, Basso, M D, Liu, Q-Y, Crandall, D L, Nambi, P
Izdano 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...

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

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

od 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.
izdano v Genome Announc (2016)

Proceed with Care: Direct Predictive Testing for Huntington Disease

od 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.
Izdano 1994