Molecular cytogenetic characterisation of a small ring X chromosome in a Turner patient and in a male patient with congenital abnormalities: role of X inactivation.

Author:

Callen D F,Eyre H J,Dolman G,Garry-Battersby M B,McCreanor J R,Valeba A,McGill J J

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference21 articles.

1. Chromosomal origin of small ring marker chromosomes in man: characterization by molecular genetics;Callen, D.F.; Eyre, H.J.; Ringenbergs, M.L.; Freemantle, C.J.; Woodroffe, P.; Haan, E.A.;Am Jf Hum Genet,1991

2. A non-isotopic in situ hybridisation study of the chromosomal origin of 15 supernumerary marker chromosomes in man;Crolla, J.A.; Dennis, N.R.; Jacobs, P.A.;J7 Med Genet,1992

3. Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes;Callen, D.F.; Eyre, H.; Yip, M.Y.; Freemantle, J.; Haan, E.A.;Am J Med Genet,1992

4. Efficient identification of marker chromosomes in 27 patients by stepwise hybridization with alpha-satellite DNA probes;Plattner, R.; Heerema, N.A.; Yurov, Y.B.; Palmer, C.G.;Hum Genet,1993

5. Characterisation of supernumerary ring marker chromosomes by fluorescence in situ hybridization (FISH);Blennow, E.; Anneren, G.; Bui, T.H.; Berggren, E.; Asadi, E.; Nordenskjold, M.;Am J Hum Genet,1993

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2. Epigenetics and genomics in Turner syndrome;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2019-02-27

3. Prenatal Diagnosis of Sex Chromosome Abnormalities;Genetic Disorders and the Fetus;2015-11-23

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