This site needs JavaScript to work properly. Please enable it to take advantage of the complete set of features!

Skip to main page content

Add to Collections

Your saved search

Name of saved search:

Search terms:

Test search terms

Would you like email updates of new search results?

Yes
No

Email: (change)

Frequency:

Which day?

Which day?

Report format:

Send at most:

Send even when there aren't any new results

Optional text in email:

Your RSS Feed

. 1962 Jun;14(2):107-24.

Enlarged satellites as a familial chromosome marker

H L COOPER, K HIRSCHHORN

PMID: 13881132
PMCID: PMC1932273

Enlarged satellites as a familial chromosome marker

H L COOPER et al. Am J Hum Genet. 1962 Jun.

. 1962 Jun;14(2):107-24.

Authors

H L COOPER, K HIRSCHHORN

PMID: 13881132
PMCID: PMC1932273

No abstract available

PubMed Disclaimer

Similar articles

A novel combined 15q11.2 duplication and a bisatellited supernumerary marker derived from chromosome 22: molecular characterization of the marker.
Dutta UR, Vempally S, Ranganath P, Dalal A. Dutta UR, et al. Gene. 2014 Apr 10;539(1):162-7. doi: 10.1016/j.gene.2014.02.002. Epub 2014 Feb 5. Gene. 2014. PMID: 24508374
Silver staining of the supernumerary chromosome in the cat-eye syndrome.
Petit P, Godart S, Fryns JP. Petit P, et al. Ann Genet. 1980;23(2):114-6. Ann Genet. 1980. PMID: 6156636
[Spectral karyotyping of seven prenatally detected marker chromosomes and complex chromosome aberrations].
Song HL, Chen BJ, Fang Q, Xie YJ, Lin SB, Wu JZ. Song HL, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Aug;29(4):393-7. doi: 10.3760/cma.j.issn.1003-9406.2012.04.004. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 22875493 Chinese.
Identification of marker chromosomes in thirteen patients using FISH probing.
Daniel A, Malafiej P, Preece K, Chia N, Nelson J, Smith M. Daniel A, et al. Am J Med Genet. 1994 Oct 15;53(1):8-18. doi: 10.1002/ajmg.1320530103. Am J Med Genet. 1994. PMID: 7802042 Review.
[Analysis of disease-associated marker chromosomes using chromosome sorter].
Minoshima S, Shimizu N. Minoshima S, et al. Tanpakushitsu Kakusan Koso. 1996 Nov;41(15 Suppl):2174-81. Tanpakushitsu Kakusan Koso. 1996. PMID: 8952379 Review. Japanese. No abstract available.

See all similar articles

Cited by

[Chromosome studies in couples with repeated abortions].
Rott HD, Richter E, Rummel WD, Schwanitz G. Rott HD, et al. Arch Gynakol. 1972;213(2):110-8. doi: 10.1007/BF00667668. Arch Gynakol. 1972. PMID: 4678743 German.
A 13-15/21 translocation chromosome in carrier father and mongol son.
SERGOVICH FR, SOLTAN HC, CARR DH. SERGOVICH FR, et al. Can Med Assoc J. 1962 Oct 20;87(16):852-8. Can Med Assoc J. 1962. PMID: 13988069 Free PMC article.
A further example of familial Gp+ associated with trisomy G.
Subrt I. Subrt I. Humangenetik. 1970;9(1):86-90. doi: 10.1007/BF00696017. Humangenetik. 1970. PMID: 4249864 No abstract available.
[To the genetics and clinical aspects of small chromosome aberrations. A chromosome Gp-h and a chromosome Gs- in one family].
Wolf U, Reinwein H, Lohmann H. Wolf U, et al. Humangenetik. 1968;5(2):107-18. doi: 10.1007/BF00278671. Humangenetik. 1968. PMID: 5662646 German. No abstract available.
[Enlargement of the short arm region of a small acrocentric chromosome].
Vormittag W, Kühböck J, Weninger M. Vormittag W, et al. Humangenetik. 1972;14(2):112-21. doi: 10.1007/BF00273294. Humangenetik. 1972. PMID: 5026841 German. No abstract available.

See all "Cited by" articles

References

1. Am J Hum Genet. 1961 Jun;13(2):205-13 - PubMed
1. Nature. 1961 Dec 23;192:1214-5 - PubMed
1. Am J Hum Genet. 1959 Mar;11(1):63-79 - PubMed
1. Am J Hum Genet. 1960 Mar;12:104-17 - PubMed
1. Proc Natl Acad Sci U S A. 1958 Dec 15;44(12):1229-37 - PubMed

MeSH terms

Actions
Actions
Actions
Actions

Substances

Actions

LinkOut - more resources

Full Text Sources
- Europe PubMed Central
- PubMed Central