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

. 1961 Aug 26;2(7200):462-3.

doi: 10.1016/s0140-6736(61)92432-1.

The Denver classification and group III

S MULDAL, C H OCKEY

PMID: 13773668
DOI: 10.1016/s0140-6736(61)92432-1

The Denver classification and group III

S MULDAL et al. Lancet. 1961.

. 1961 Aug 26;2(7200):462-3.

doi: 10.1016/s0140-6736(61)92432-1.

Authors

S MULDAL, C H OCKEY

PMID: 13773668
DOI: 10.1016/s0140-6736(61)92432-1

No abstract available

PubMed Disclaimer

Similar articles

Investigation of family showing transmission of a 13-15 chromosomal translocation (Denver classification).
WALKER S, HARRIS R. WALKER S, et al. Br Med J. 1962 Jul 7;2(5296):25-6. doi: 10.1136/bmj.2.5296.25. Br Med J. 1962. PMID: 14004623 Free PMC article. No abstract available.
Familial 13-15 translocation abnormality (Denver classification) associated with one case of cerebral palsy. Preliminary report.
JAGIELLO GM. JAGIELLO GM. N Engl J Med. 1963 Jul 11;269:66-9. doi: 10.1056/NEJM196307112690202. N Engl J Med. 1963. PMID: 13964466 No abstract available.
Relationship between G band number and chromosome length from prophase to metaphase.
Jagielski J, Haus O. Jagielski J, et al. Acta Physiol Pol. 1983 Jan-Feb;34(1):77-84. Acta Physiol Pol. 1983. PMID: 6637533
Marker chromosomes.
Rao KP, Belogolovkin V. Rao KP, et al. Fetal Pediatr Pathol. 2013 Apr;32(2):97-112. doi: 10.3109/15513815.2012.681425. Epub 2012 May 15. Fetal Pediatr Pathol. 2013. PMID: 22587446 Review.
Molecular cytogenetic study of supernumerary marker chromosomes in an unselected group of children.
Gravholt CH, Friedrich U. Gravholt CH, et al. Am J Med Genet. 1995 Mar 13;56(1):106-11. doi: 10.1002/ajmg.1320560124. Am J Med Genet. 1995. PMID: 7747772 Review.

See all similar articles

Cited by

[Chromosome anomalies in the blood cells of a child with multiple abnormalities].
PFEIFFER RA, SCHELLONG G, KOSENOW W. PFEIFFER RA, et al. Klin Wochenschr. 1962 Oct 15;40:1058-67. doi: 10.1007/BF01484591. Klin Wochenschr. 1962. PMID: 13943080 German. No abstract available.
[ON THE CLINICAL ASPECTS AND HISTOPATHOLOGY OF PRIMARY MALE HYPOGONADISM. 2. CASTRATISM AND SO-CALLED KLINEFELTER'S SYNDROME AS DISEASE FORMS WITH KNOWN ETIOLOGY].
HORNSTEIN O. HORNSTEIN O. Arch Klin Exp Dermatol. 1963 Sep 2;217:149-95. Arch Klin Exp Dermatol. 1963. PMID: 14098769 Review. German. No abstract available.
The demonstration of secondary constrictions in human chromosomes by means of a new technique.
SASAKI MS, MAKINO S. SASAKI MS, et al. Am J Hum Genet. 1963 Mar;15(1):24-33. Am J Hum Genet. 1963. PMID: 13986623 Free PMC article. No abstract available.

MeSH terms

Actions
Actions

LinkOut - more resources

Full Text Sources
- Elsevier Science