Familial pericentric inversion 19.

Author:

Jordan D K,Taysi K,Blackwell N L

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference9 articles.

1. An analysis of the break points of structural rearrangements in man;Jacobs, P.A.; Buckton, K.E.; Cunningham, C.; Newton, M.;J Med Geniet,1974

2. A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities;Hamerton, J.L.; Canning, N.; Ray, M.; Smith, S.;Clin Genet,1975

3. Familial pericentric inversion of chromosome 19, inv(l9)(pl3q13) with a note on genetic counselling of pericentric inversion carriers;Sutherland, G.R.; Gardiner, A.J.; Carter, R.F.;Clin Genet,1976

4. Inversion 19 and isochromosome short arm 17 or 18;Nielsen, J.; Homma, A.; Holm, V.;Hunt Genet,1977

5. Variation in the centromeric banding of chromosome 19;Crossen, P.E.;Clin Genet,1975

Cited by 12 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

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

2. Chromosome 19;Human Chromosome Variation: Heteromorphism and Polymorphism;2011

3. Monosomy 19pter and trisomy 19q13-qter in two siblings arising from a maternal pericentric inversion: Clinical data and molecular characterization;European Journal of Medical Genetics;2008-11

4. Duplication 19q13-qter and deletion 19p13-pter arising from an inversion (19)(p13.3q13.3) of maternal origin;European Journal of Medical Genetics;2006-11

5. Plates;Atlas of Human Chromosome Heteromorphisms;2004

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