A FAMILY APPARENTLY SHOWING TRANSMISSION OF A TRANSLOCATION BETWEEN CHROMOSOME 3 AND ONE OF THE 'X-6-12' OR 'C' GROUP
- PMID: 14205979
- PMCID: PMC1012720
- DOI: 10.1136/jmg.1.1.27
A FAMILY APPARENTLY SHOWING TRANSMISSION OF A TRANSLOCATION BETWEEN CHROMOSOME 3 AND ONE OF THE 'X-6-12' OR 'C' GROUP
Similar articles
-
A SMALL AUTOSOMAL RING CHROMOSOME IN A FEMALE INFANT WITH CONGENITAL MALFORMATIONS.Ann Hum Genet. 1963 Nov;27:189-95. doi: 10.1111/j.1469-1809.1963.tb00212.x. Ann Hum Genet. 1963. PMID: 14081490 No abstract available.
-
FERTILITY IN AN XY/XXY MALE MARRIED TO A TRANSLOCATION HETEROZYGOTE.J Med Genet. 1964 Sep;1(1):35-8. doi: 10.1136/jmg.1.1.35. J Med Genet. 1964. PMID: 14205982 Free PMC article. No abstract available.
-
A case with 46, XX, del (11) (q21).Clin Genet. 1974;6(2):90-7. doi: 10.1111/j.1399-0004.1974.tb00637.x. Clin Genet. 1974. PMID: 4279151 No abstract available.
-
Human genetics in Poland.Hum Biol. 1973 Feb;45(1):5-21. Hum Biol. 1973. PMID: 4266513 Review. No abstract available.
-
[SOME PRACTICAL ACHIEVEMENTS IN MEDICAL GENETICS].Vestn Akad Med Nauk SSSR. 1963;18:14-22. Vestn Akad Med Nauk SSSR. 1963. PMID: 14157496 Review. Russian. No abstract available.
Cited by
-
A translocation t (Bq+: Cq-) in a West Indian family and a report of a second family showing a possible long arm group B translocation.Arch Dis Child. 1969 Feb;44(233):106-12. doi: 10.1136/adc.44.233.106. Arch Dis Child. 1969. PMID: 5765976 Free PMC article. No abstract available.
-
Apparent monosomy of a G autosome in a Jamaican infant.J Med Genet. 1966 Dec;3(4):290-2. doi: 10.1136/jmg.3.4.290. J Med Genet. 1966. PMID: 16178089 Free PMC article. No abstract available.
-
X-autosome translocation with a breakpoint in Xq22 in a fertile woman and her 47,XXX infertile daughter.Hum Genet. 1981;59(4):290-6. doi: 10.1007/BF00295460. Hum Genet. 1981. PMID: 7333583
-
Familial partial trisomy of the long arm of chromosome 3 (3q).Arch Dis Child. 1979 Feb;54(2):135-8. doi: 10.1136/adc.54.2.135. Arch Dis Child. 1979. PMID: 434890 Free PMC article.
-
Turner syndrome and female sex chromosome aberrations: deduction of the principal factors involved in the development of clinical features.Hum Genet. 1995 Jun;95(6):607-29. doi: 10.1007/BF00209476. Hum Genet. 1995. PMID: 7789944 Review.
References
-
- Lancet. 1962 Oct 13;2(7259):784 - PubMed
MeSH terms
Substances
LinkOut - more resources
Full Text Sources