Chromosomal Variation in Man: A Catalog of Chromosomal Variants and Anomalies

Por Brook, J D
Publicado em 1987

A polymorphic DNA clone which maps to 19p13.2----19q12 (D19S27).

Por Brook, J D, Shaw, D J
Publicado em 1988

An ELECTROMYOGRAPHICAL ANALYSIS OF NOXIOUS ISCHAEMIC WORK

Por Brook, J. D., Cooper, D., Hamley, E. J., Saville, B. F.
Publicado em 1967

A polymorphic DNA clone which maps to 19q13.2–19qter (D19S62)

Por Brook, J.D., Walsh, K.V., Harley, H.G., Rundle, S.A., Shaw, D.J.
Publicado em 1990

RFLP for a DNA clone which maps to 19q13.2–19qter (D19S63)

Por Brook, J.D., Harley, H.G., Rundle, S.A., Walsh, K.V., Shaw, D.J.
Publicado em 1990

RFLP for a DNA clone which maps to 19q13.2–19qter (D19S63)

Por Brook, J.D., Harley, H.G., Rundle, S.A., Walsh, K.V., Shaw, D.J.
Publicado em 1990

A study of DNA methylation in myotonic dystrophy.

Por Shaw, D J, Chaudhary, S, Rundle, S A, Crow, S, Brook, J D, Harper, P S, Harley, H G
Publicado em 1993

Close linkage of the human cytochrome P450IIA and P450IIB gene subfamilies: implications for the assignment of substrate specificity.

Por Miles, J S, Bickmore, W, Brook, J D, McLaren, A W, Meehan, R, Wolf, C R
Publicado em 1989

Minimal expression of myotonic dystrophy: a clinical and molecular analysis.

Por Reardon, W, Harley, H G, Brook, J D, Rundle, S A, Crow, S, Harper, P S, Shaw, D J
Publicado em 1992

Gene mapping and chromosome 19.

Por Shaw, D J, Brook, J D, Meredith, A L, Harley, H G, Sarfarazi, M, Harper, P S
Publicado em 1986

Targeted integration of adeno-associated virus (AAV) into human chromosome 19.

Por Samulski, R J, Zhu, X, Xiao, X, Brook, J D, Housman, D E, Epstein, N, Hunter, L A
Publicado em 1991

A novel human cytochrome P450 gene (P450IIB): chromosomal localization and evidence for alternative splicing.

Por Miles, J S, Spurr, N K, Gough, A C, Jowett, T, McLaren, A W, Brook, J D, Wolf, C R
Publicado em 1988

A HindIII polymorphism identified by a DNA clone which maps to chromosome 17 (D17S245)

Por Brook, J.D., Upadhyaya, M., Broadhead, W., Rundle, S.A., Walsh, K.V., Harley, H.G., Shaw, D.J.
Publicado em 1990

Identification of new DNA markers close to the myotonic dystrophy locus.

Por Brook, J D, Harley, H G, Walsh, K V, Rundle, S A, Siciliano, M J, Harper, P S, Shaw, D J
Publicado em 1991

Exon amplification: a strategy to isolate mammalian genes based on RNA splicing.

Por Buckler, A J, Chang, D D, Graw, S L, Brook, J D, Haber, D A, Sharp, P A, Housman, D E
Publicado em 1991

Application of a closely linked polymorphism of restriction fragment length to counselling and prenatal testing in families with myotonic dystrophy.

Por Meredith, A L, Huson, S M, Lunt, P W, Sarfarazi, M, Harley, H G, Brook, J D, Shaw, D J, Harper, P S
Publicado em 1986

Detection of linkage disequilibrium between the myotonic dystrophy locus and a new polymorphic DNA marker.

Por Harley, H G, Brook, J D, Floyd, J, Rundle, S A, Crow, S, Walsh, K V, Thibault, M C, Harper, P S, Shaw, D J
Publicado em 1991

Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy.

Por Harley, H G, Rundle, S A, MacMillan, J C, Myring, J, Brook, J D, Crow, S, Reardon, W, Fenton, I, Shaw, D J, Harper, P S
Publicado em 1993

A translocation at 12q2 refines the interval containing the Holt-Oram syndrome 1 gene.

Por Terrett, J. A., Newbury-Ecob, R., Smith, N. M., Li, Q. Y., Garrett, C., Cox, P., Bonnet, D., Lyonnet, S., Munnich, A., Buckler, A. J., Brook, J. D.
Publicado em 1996