?Jumping? satellites in three generations: A warning for paternity tests and prenatal diagnosis-Reference-Cited by-同舟云学术

?Jumping? satellites in three generations: A warning for paternity tests and prenatal diagnosis

Published:1976 Issue:3 Volume:34 Page:315-318
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Gimelli G.,Porro E.,Santi F.,Scappaticci Susi,Zuffardi Orsetta

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00295297.pdf

Reference4 articles.

1. Hamerton, J. J., Canning, N., Ray, M., Smith, S.: A cytogenetic survey of 14,069 newborn infants. Clin. Genet. 8, 223 (1975)

2. Hauge, M., Poulsen, H., Halberg, A., Mikkelsen, M.: The value of fluorescence markers in the distinction between maternal and fetal chromosomes. Humangenetik 26, 187 (1975)

3. Hultén, M., Lindsten, J.: The behaviour of structural aberrations at male meiosis. In: Human population cytogenetics, Patricia A. Jacobs, W. H. Price, Pamela Law, eds., p. 23. Edinburgh University Press 1970

4. Jonasson, J., Lindsten, J., Lundborg, R., Kissmeyer-Nielsen, F., Lamm, L. U., Bruun Petersen, G., Therkelsen, A. J.: HL-A antigens and heteromorphic fluorescence characters of chromosomes in prenatal paternity investigation. Nature (Lond.) 236, 312 (1972)

Cited by 17 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. Short arms of human acrocentric chromosomes and the completion of the human genome sequence;Genome Research;2022-03-31

2. Chromosomal instability in first trimester miscarriage: a common cause of pregnancy loss?;Translational Pediatrics;2018-07

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

4. Chromosome 22;Human Chromosome Variation: Heteromorphism and Polymorphism;2011

5. Chromosome 21;Human Chromosome Variation: Heteromorphism and Polymorphism;2011