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

. 1971 Sep;8(3):358-63.

doi: 10.1136/jmg.8.3.358.

Somatic stigmata of Turner's syndrome in a patient with 46,XXq-

M Bocian, E Krmpotic, K Szego, I M Rosenthal

PMID: 5097143
PMCID: PMC1469177
DOI: 10.1136/jmg.8.3.358

Somatic stigmata of Turner's syndrome in a patient with 46,XXq-

M Bocian et al. J Med Genet. 1971 Sep.

. 1971 Sep;8(3):358-63.

doi: 10.1136/jmg.8.3.358.

Authors

M Bocian, E Krmpotic, K Szego, I M Rosenthal

PMID: 5097143
PMCID: PMC1469177
DOI: 10.1136/jmg.8.3.358

No abstract available

PubMed Disclaimer

Similar articles

Fluorescence and autoradiographic studies in patients with Turner's syndrome and 46,XXp- and 46,XXq- karyotypes.
Boczkowski K, Mikkelsen M. Boczkowski K, et al. J Med Genet. 1973 Dec;10(4):350-5. doi: 10.1136/jmg.10.4.350. J Med Genet. 1973. PMID: 4129970 Free PMC article.
A VERY LARGE METACENTRIC CHROMOSOME IN A WOMAN WITH SYMPTOMS OF TURNER'S SYNDROME.
WIELIE G, COENEGRACHT JM, STALDER G. WIELIE G, et al. Cytogenetics. 1964;3:427-40. doi: 10.1159/000129831. Cytogenetics. 1964. PMID: 14267135 No abstract available.
A 47,XXq-Y Klinefelter male.
Chandra HS, Reddy GN, Peter J, Venkatachalaiah G. Chandra HS, et al. J Med Genet. 1971 Dec;8(4):530-2. doi: 10.1136/jmg.8.4.530. J Med Genet. 1971. PMID: 5149539 Free PMC article. No abstract available.
SEX CHROMATIN.
MITTWOCH U. MITTWOCH U. J Med Genet. 1964 Sep;1(1):50-76. doi: 10.1136/jmg.1.1.50. J Med Genet. 1964. PMID: 14205986 Free PMC article. Review. No abstract available.
[CHROMOSOME MOSAICS].
BERNARD R, GIRAUD F. BERNARD R, et al. Mars Med. 1964;101:601-22. Mars Med. 1964. PMID: 14207925 Review. French. No abstract available.

See all similar articles

Cited by

The similarity of phenotypic effects caused by Xp and Xq deletions in the human female: a hypothesis.
Therman E, Susman B. Therman E, et al. Hum Genet. 1990 Jul;85(2):175-83. doi: 10.1007/BF00193192. Hum Genet. 1990. PMID: 2370045
A case of long arm deletion of the X chromosome in a patient with secondary amenorrhea.
Branković S, Laća Z, Dramusić V, Ivanović M, Morić-Petrović S. Branković S, et al. Hum Genet. 1979 Apr 17;48(1):139-42. doi: 10.1007/BF00273289. Hum Genet. 1979. PMID: 457130
Cytologic and molecular analysis of 46,XXq- cells to identify a DNA segment that might serve as a probe for a putative human X chromosome inactivation center.
Tantravahi U, Kirschner DA, Beauregard L, Page L, Kunkel L, Latt S. Tantravahi U, et al. Hum Genet. 1983;64(1):33-8. doi: 10.1007/BF00289475. Hum Genet. 1983. PMID: 6347866
Turner syndrome and female sex chromosome aberrations: deduction of the principal factors involved in the development of clinical features.
Ogata T, Matsuo N. Ogata T, et al. Hum Genet. 1995 Jun;95(6):607-29. doi: 10.1007/BF00209476. Hum Genet. 1995. PMID: 7789944 Review.
Primary thyroid failure presenting as a pituitary tumour.
Daggett P, Harsoulis P, Kuku SF, Pearse E, Fraser TR. Daggett P, et al. Postgrad Med J. 1975 Feb;51(592):85-9. doi: 10.1136/pgmj.51.592.85. Postgrad Med J. 1975. PMID: 1114151 Free PMC article.

See all "Cited by" articles

References

1. J Med Genet. 1970 Mar;7(1):1-4 - PubMed
1. Lancet. 1961 Jun 3;1(7188):1183-9 - PubMed
1. Exp Cell Res. 1960 Sep;20:613-6 - PubMed
1. Lancet. 1963 Apr 20;1(7286):863-5 - PubMed
1. Proc Natl Acad Sci U S A. 1964 May;51:779-86 - PubMed

MeSH terms

Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions

Substances

Actions
Actions

LinkOut - more resources

Full Text Sources