Chromosome imbalance, normal phenotype, and imprinting.

Author:

Bortotto L,Piovan E,Furlan R,Rivera H,Zuffardi O

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference33 articles.

1. Human chromosomal heteromorphisms: nature and clinical significance;Verma, R.S.; Dosik, H.;Int Rev Cytol,1980

2. Aspects of evaluation, significance and evolution of human C-band heteromorphism;Erdtmann, B.;Hum Genet,1982

3. Molecular analysis of an unbalanced deletion of the short arm of chromosomes that produces no phenotypes;Overhauser, J.; Golbus, M.S.; Schonberg, S.A.; Wasmutt, J.J.;Am J Hum Genet,1986

4. A G-band study of chromosomes in liveborn infants;Buckton, K.E.; O'Riordan, M.L.; Ratcliffe, S.;Ann Hum Genet,1980

5. Two unusual G-bands variants of the short arm of chromosome 9;Sutherland, G.R.; Eyre, H.;Clin Genet,1981

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

3. Euchromatic Variants;Human Chromosome Variation: Heteromorphism, Polymorphism and Pathogenesis;2017

4. Inherited interstitial 16q21 deletion of 5.8 Mb without apparent phenotypic effect in three generations of a family: An array-CGH study;American Journal of Medical Genetics Part A;2011-09-09

5. The distal partial trisomy 1q syndrome and dystonic tremor;Parkinsonism & Related Disorders;2011-02

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