FMR1 fully expanded mutation with minimal methylation in a high functioning fragile X male.

Yazar: Loesch, D Z
Baskı/Yayın Bilgisi 1997

Clinical features and reproductive patterns in fragile X female heterozygotes.

Yazar: Loesch, D Z, Hay, D A
Baskı/Yayın Bilgisi 1988

Fixed and random effects in the variation of the finger ridge count: a study of fragile-X families.

Yazar: Loesch, D Z, Huggins, R M
Baskı/Yayın Bilgisi 1992

Expansion of the CGG repeat in fragile X in the FMR1 gene depends on the sex of the offspring.

Yazar: Loesch, D Z, Huggins, R, Petrovic, V, Slater, H
Baskı/Yayın Bilgisi 1995

Evidence for Polygenic Epistatic Interactions in Man?

Yazar: Heath, A. C., Martin, N. G., Eaves, L. J., Loesch, D.
Baskı/Yayın Bilgisi 1984

Timing and genetic rapport between growth in skeletal maturity and height around puberty: similarities and differences between girls and boys.

Yazar: Loesch, D Z, Hopper, J L, Rogucka, E, Huggins, R M
Baskı/Yayın Bilgisi 1995

Genotype-phenotype relationships in fragile X syndrome: a family study.

Yazar: Loesch, D Z, Huggins, R, Hay, D A, Gedeon, A K, Mulley, J C, Sutherland, G R
Baskı/Yayın Bilgisi 1993

White matter changes in basis pontis in small expansion FMR1 allele carriers with parkinsonism

Yazar: Loesch, D.Z., Kotschet, K., Trost, N., Greco, C. M., Kinsella, G., Slater, H.R., Venn, A., Horne, M.
Baskı/Yayın Bilgisi 2011

FRAXE and mental retardation.

Yazar: Mulley, J C, Yu, S, Loesch, D Z, Hay, D A, Donnelly, A, Gedeon, A K, Carbonell, P, López, I, Glover, G, Gabarrón, I
Baskı/Yayın Bilgisi 1995

Experience with direct molecular diagnosis of fragile X.

Yazar: Mulley, J C, Yu, S, Gedeon, A K, Donnelly, A, Turner, G, Loesch, D, Chapman, C J, Gardner, R J, Richards, R I, Sutherland, G R
Baskı/Yayın Bilgisi 1992

Fragile-X syndrome: Unique genetics of the heritable unstable element

Yazar: Yu, S., Mulley, J., Loesch, D., Turner, G., Donnelly, A., Gedeon, A., Hillen, D., Kremer, E., Lynch, M., Pritchard, M., Sutherland, G. R., Richards, R. I.
Baskı/Yayın Bilgisi 1992