X inactivation patterns in female monozygotic twins and their families.

Author:

Watkiss E,Webb T,Rysiecki G,Girdler N,Hewett E,Bundey S

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference30 articles.

1. Christmas disease in one of a pair of monozygotic twin girls, possibly the effect of Lyonisation;Revesz, T.; Schuler, D.; Goldschmidt, B.; Elodi, S.;J Med Genet,1972

2. Frequency and replication status of the fragile X, fra(X)(q27-28), in a pair of monozygotic twins of markedly differing intelligence;Tuckerman, E.; Webb, T.; Bundey, S.E.;J Med Genet,1985

3. Fragile X syndrome and the (CGG)n mutation: two families with discordant MZ twins;Kruyer, H.; Mila, M.; Glover, G.; Carbonell, P.; Ballesta, F.; Estivill, X.;Am J Hum Genet,1994

4. Colour vision deficiency in one of two presumably monozygotic twins with secondary amenorrhoea;Philip, J.; Vogelius Andersen, C.H.; Dreyer, V.;Ann Hum Genet

5. Different patterns of X inactivation in MZ twins discordant for redgreen colour-vision deficiency;Jorgenson, A.L.; Philip, J.; Raskind, W.H.;Am 7 Hum Genet,1992

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