Mendelian cytogenetics. Chromosome rearrangements associated with mendelian disorders.

Author:

Tommerup N

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference204 articles.

1. Expression of an X-linked recessive disease in a female due to nonrandom inactivation of the X chromosome;Verellen, C.; Markovic, V.; DeMeyer, R.;Am Hum Genet,1978

2. Muscular dystrophy in an X; 1 translocation female suggests that Duchenne locus is on X chromosome short arm;Lindenbaum, R.H.; Clarke, G.; Patel, C.;Med Genet,1979

3. Report of the committee on clinical disorders and chromosomal deletion syndromes (HGMI 1);Frezal, J.; Schinzel, A.;Cytogenet Cell Genet,1991

4. Positional cloning: let's not call it reverse anymore;Collins, F.S.;Nature Genet,1992

5. Chromosomal abnormalities in mendelian disorders;Edwards, J.H.;Lancet,1982

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