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

Case Reports

. 1970 Apr;45(4):677-86.

Cytogenetic analysis of a boy with the XXXY syndrome: origin of the X-chromosomes

R M Greenstein, D J Harris, L Luzzatti, H M Cann

PMID: 5438170

Case Reports

Cytogenetic analysis of a boy with the XXXY syndrome: origin of the X-chromosomes

R M Greenstein et al. Pediatrics. 1970 Apr.

. 1970 Apr;45(4):677-86.

Authors

R M Greenstein, D J Harris, L Luzzatti, H M Cann

PMID: 5438170

No abstract available

PubMed Disclaimer

Similar articles

[49,XXXXY syndrome in a 5-year-old boy].
Wiśniewski L, Krajewska-Walasek M, Lech H, Mospinek M. Wiśniewski L, et al. Pediatr Pol. 1980 Jan;55(1):81-6. Pediatr Pol. 1980. PMID: 7189276 Polish. No abstract available.
Radioulnar synostosis, behavioral disturbance, and XYY chromosomes.
Cleveland WW, Arias D, Smith GF. Cleveland WW, et al. J Pediatr. 1969 Jan;74(1):103-6. doi: 10.1016/s0022-3476(69)80014-4. J Pediatr. 1969. PMID: 5782813 No abstract available.
XXXY chromosomal abnormality in a child.
McGann BR, Alexander M, Fox FA. McGann BR, et al. Calif Med. 1970 Jan;112(1):30-2. Calif Med. 1970. PMID: 5410731 Free PMC article. No abstract available.
[The 48,XXXX syndrome: study of psychomotor development from birth to 11 years of age and review of the literature].
Plauchu H, Ollagnon-Roman E, Armand JP, Robert JM. Plauchu H, et al. Ann Genet. 1988;31(2):105-10. Ann Genet. 1988. PMID: 3041908 Review. French.
X-chromosome inactivation and developmental patterns in mammals.
Lyon MF. Lyon MF. Biol Rev Camb Philos Soc. 1972 Jan;47(1):1-35. doi: 10.1111/j.1469-185x.1972.tb00969.x. Biol Rev Camb Philos Soc. 1972. PMID: 4554151 Review. No abstract available.

See all similar articles

Cited by

The influence of inactive chromosomes on human development. Anomalous sex chromosome complements and the phenotype.
Barlow P. Barlow P. Humangenetik. 1973;17(2):105-36. doi: 10.1007/BF00277906. Humangenetik. 1973. PMID: 4691146 No abstract available.
Parental origin of the extra chromosomes in polysomy X.
Leal CA, Belmont JW, Nachtman R, Cantu JM, Medina C. Leal CA, et al. Hum Genet. 1994 Oct;94(4):423-6. doi: 10.1007/BF00201605. Hum Genet. 1994. PMID: 7927341
Abnormalities of human sex chromosomes. VI. Monozygotic twins with the complement 48,XXXY.
Simpson JL, Morillo-Cucci G, Horwith M, Stiefel FH, Feldman F, German J. Simpson JL, et al. Humangenetik. 1974 Mar 28;21(4):301-8. Humangenetik. 1974. PMID: 4857900 No abstract available.
XXXX syndrome: case report, and a note on genetic counselling and fertility.
Gardner RJ, Veale AM, Sands VE, Holdaway MD. Gardner RJ, et al. Humangenetik. 1973;17(4):323-30. doi: 10.1007/BF00273187. Humangenetik. 1973. PMID: 4694514 No abstract available.
Analysis of non-disjunction in sex chromosome tetrasomy and pentasomy.
Hassold T, Pettay D, May K, Robinson A. Hassold T, et al. Hum Genet. 1990 Oct;85(6):648-50. doi: 10.1007/BF00193591. Hum Genet. 1990. PMID: 1977687

See all "Cited by" articles

Publication types

Actions

MeSH terms

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

Substances

Actions
Actions

LinkOut - more resources

Molecular Biology Databases
- The Weizmann Institute of Science GeneCards and MalaCards databases