Chromosome 18 abnormalities in a family with a translocation t(18p--, 21p+)
- PMID: 5663940
- DOI: 10.1111/j.1365-2788.1968.tb00254.x
Chromosome 18 abnormalities in a family with a translocation t(18p--, 21p+)
Similar articles
-
An inherited small extra chromosome: a mother with 46,XX,t(17;22)(pl;ql) and a son with 47,XY,+der(22)mat.J Med Genet. 1973 Dec;10(4):379-84. doi: 10.1136/jmg.10.4.379. J Med Genet. 1973. PMID: 4129973 Free PMC article.
-
Familial C-G translocation in three relatives associated with severe mental retardation, short stature, unusual dermatoglyphics and other malformations.J Ment Defic Res. 1971 Jun;15(2):136-46. doi: 10.1111/j.1365-2788.1971.tb01151.x. J Ment Defic Res. 1971. PMID: 5559234 No abstract available.
-
A short, retarded child with a deletion of the short arm of chromosome 18 (18p-).Clin Pediatr (Phila). 1973 Jan;12(1):42-6. doi: 10.1177/000992287301200111. Clin Pediatr (Phila). 1973. PMID: 4345621 No abstract available.
-
Familial mental retardation in a family with an inherited chromosome rearrangement.J Med Genet. 1974 Dec;11(4):353-66. doi: 10.1136/jmg.11.4.353. J Med Genet. 1974. PMID: 4140909 Free PMC article.
-
[Deficiency at the short arm of chromosome No. 18 (46, XX, 18p-). A uniform abnormality syndrome].Monatsschr Kinderheilkd (1902). 1968 Sep;116(9):511-4. Monatsschr Kinderheilkd (1902). 1968. PMID: 5682047 German. No abstract available.
Cited by
-
Azoospermia and trisomy 18p syndrome: a fortuitous association? A patient report and a review of the literature.Mol Cytogenet. 2015 Jun 4;8:34. doi: 10.1186/s13039-015-0141-8. eCollection 2015. Mol Cytogenet. 2015. PMID: 26042156 Free PMC article.
-
[Ring chromosome 18. 18p-/18q- -deletion-syndrome].Humangenetik. 1972;15(4):289-318. doi: 10.1007/BF00281730. Humangenetik. 1972. PMID: 4565746 Review. German. No abstract available.
-
Partial monosomies 18. Review of cytogenetical and phenotypical variants.Humangenetik. 1972;15(3):203-22. doi: 10.1007/BF00702354. Humangenetik. 1972. PMID: 4563067 Review. No abstract available.
-
Trisomy 18 phenotype in a patient with an isopseudodicentric 18 chromosome.J Med Genet. 1984 Apr;21(2):151-3. doi: 10.1136/jmg.21.2.151. J Med Genet. 1984. PMID: 6716418 Free PMC article.