Chiasma distribution, genetic lengths, and recombination fractions: a comparison between chromosomes 15 and 16.

Por Saadallah, N, Hultén, M
Publicado em 1983

What is to be done with the XYY fetus?

Por Farrant, W, Hulten, M
Publicado em 1979

Chromosome in situ suppression hybridisation in human male meiosis.

Por Goldman, A S, Hultén, M A
Publicado em 1992

Extra euchromatic band in the qh region of chromosome 9.

Por Docherty, Z, Hultén, M A
Publicado em 1985

Chiasma derived genetic maps and recombination fractions: chromosome 13 with reference to the proposed 13q14 retinoblastoma locus.

Por Palmer, R W, Hultén, M A
Publicado em 1982

FISH analysis on spontaneously arising micronuclei in the ICF syndrome.

Por Stacey, M, Bennett, M S, Hulten, M
Publicado em 1995

Does junk DNA regulate gene expression in humans?

Por Hultén, M A, Stacey, M, Armstrong, S J
Publicado em 1995

A TaqI RFLP in the region of the HPRT locus

Por Renwick, P., Raybould, M., Birley, A., Hultén, M.
Publicado em 1991

De novo tandem duplication 17p11→cen

Por Docherty, Z, Hultén, M A, Honeyman, M M
Publicado em 1983

A Hinf I polymorphism in the human elastin gene (ELN)

Por Raybould, M.C., Renwick, P., Birley, A., Hultén, M.
Publicado em 1992

The effect of the male contraceptive agent Gossypol on human lymphocytes in vitro: traditional chromosome breakage, micronuclei, sister chromatid exchange, and cell kinetics.

Por Tsui, Y C, Creasy, M R, Hultén, M A
Publicado em 1983

Clinical and cytogenetic diversity in Fanconi's anaemia.

Por Duckworth-Rysiecki, G, Hultén, M, Mann, J, Taylor, A M
Publicado em 1984

The prevalence of translocations in parents of children with regular trisomy 21: a possible interchromosomal effect?

Por Lindenbaum, R H, Hultén, M, McDermott, A, Seabright, M
Publicado em 1985

Integration of gene maps: chromosome 21.

Por Lawrence, S, Collins, A, Keats, B J, Hulten, M, Morton, N E
Publicado em 1993

Chromosome in situ suppression hybridisation in clinical cytogenetics.

Por Hulten, M A, Gould, C P, Goldman, A S, Waters, J J
Publicado em 1991

Distribution of the Rad51 recombinase in human and mouse spermatocytes.

Por Barlow, A L, Benson, F E, West, S C, Hultén, M A
Publicado em 1997

Homozygosity in piebald trait.

Por Hultén, M A, Honeyman, M M, Mayne, A J, Tarlow, M J
Publicado em 1987

Additional G-like chromosome in a malformed boy.

Por Fraccaro, M, Hultén, M, Jayakar, S D, Lindsjö, A, Lindsten, J, Tiepolo, L
Publicado em 1971

Genetic analysis of meiotic recombination in humans by use of sperm typing: reduced recombination within a heterozygous paracentric inversion of chromosome 9q32-q34.3.

Por Brown, G M, Leversha, M, Hulten, M, Ferguson-Smith, M A, Affara, N A, Furlong, R A
Publicado em 1998

Meiotic and sperm chromosome analysis in a male carrier of an inverted insertion (3;10)(q13.2;p14p13).

Por Goldman, A S, Martin, R H, Johannisson, R, Gould, C P, Davison, E V, Emslie, J E, Burn, J, Hultén, M A
Publicado em 1992