The fragile X syndrome.

Por Jacobs, P A
Publicado em 1991

Mutation rates of structural chromosome rearrangements in man.

Por Jacobs, P A
Publicado em 1981

The William Allan Memorial Award address: human population cytogenetics: the first twenty-five years.

Por Jacobs, P A
Publicado em 1982

Fragile Xq27.3 in female heterozygotes for the Martin-Bell syndrome.

Por Webb, T, Jacobs, P A
Publicado em 1990

Lateral asymmetry in human constitutive heterochromatin: frequency and inheritance.

Por Angell, R R, Jacobs, P A
Publicado em 1978

Chromatid associations in acrocentric chromosomes: evidence against nonrandomness.

Por Donahue, R P, Jacobs, P A
Publicado em 1982

Cytogenetic and molecular studies of trisomy 13.

Por Hassold, T, Jacobs, P A, Leppert, M, Sheldon, M
Publicado em 1987

The effect of methionine and 5-azacytidine on fragile X expression.

Por Abruzzo, M A, Mayer, M, Jacobs, P A
Publicado em 1985

Acrocentric chromosome associations in man.

Por Jacobs, P A, Mayer, M, Morton, N E
Publicado em 1976

Response to Carothers' letter.

Por Morton, N E, Jacobs, P A, Mayer, M
Publicado em 1979

Frequent small amplifications in the FMR-1 gene in fra(X) families: limits to the diagnosis of 'premutations'.

Por Macpherson, J N, Nelson, D L, Jacobs, P A
Publicado em 1992

A non-isotopic in situ hybridisation study of the chromosomal origin of 15 supernumerary marker chromosomes in man.

Por Crolla, J A, Dennis, N R, Jacobs, P A
Publicado em 1992

Further information on the identity of 47,XYY males.

Por Brown, W. M., Price, W. H., Jacobs, P. A.
Publicado em 1968

Chromosome surveys in penal institutions and approved schools.

Por Jacobs, P A, Price, W H, Richmond, S, Ratcliff, R A
Publicado em 1971

Mongols with Leukaemia

Por Baikie, A. G., Brown, W. M. Court, Jacobs, P. A.
Publicado em 1960

A family with two translocations and a polymorphism involving chromosome 14.

Por Jacobs, P A, Buckton, K E, Christie, S, Newton, M, Matthew, D
Publicado em 1974

Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of banding.

Por Jacobs, P A, Browne, C, Gregson, N, Joyce, C, White, H
Publicado em 1992

Trisomy 13 ascertained in a survey of spontaneous abortions.

Por Jacobs, P A, Hassold, T J, Henry, A, Pettay, D, Takaesu, N
Publicado em 1987

Late replicating X chromosomes in human triploidy.

Por Jacobs, P A, Matsuyama, A M, Buchanan, I M, Wilson, C
Publicado em 1979

A comparison of the clinical and cytogenetic findings in nine patients with a ring (X) cell line and 16 45,X patients.

Por Collins, A L, Cockwell, A E, Jacobs, P A, Dennis, N R
Publicado em 1994