A rare heteromorphism of chromosome 20 and reproductive loss.

Author:

Romain D R,Whyte S,Callen D F,Eyre H J

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference7 articles.

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2. LBA technique in the detection of chromosome variants. II. Chromosomes except for those with Q variants;Nakagome, Y.; Oka, S.; Matsunaga, E.;Hum Genet,1977

3. Rare chromosome 20 variants encountered during prenatal diagnosis;Petersen, M.B.,1986

4. Molecular and genetic characterisation of chromosome specific subsets of human satellite DNA;Waye, J.S.; Greig, G.; Duffy, S.J.; England, S.B.; Warburton, P.W.; Willard, H.F.;Cytogenet Cell Genet,1987

5. Sensitive system for visualising biotinylated DNA probes hybridised in situ: rapid sex determination of intact cells;Burns, J.; Chan, V.T.W.; Jonasson, J.A.; Fleming, K.A.; Taylor, S.; McGee, O.D.;J Clin Pathol,1985

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1. Chromosome Heteromorphism (Summaries);Human Chromosome Variation: Heteromorphism, Polymorphism and Pathogenesis;2017

2. References;Benign & Pathological Chromosomal Imbalances;2014

3. Chromosome 20;Human Chromosome Variation: Heteromorphism and Polymorphism;2011

4. Prenatal diagnosis of a rare inherited heterochromatic variant chromosome 4;American Journal of Medical Genetics;2004

5. Plates;Atlas of Human Chromosome Heteromorphisms;2004

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