Case Reports
doi: 10.1136/jmg.17.6.444.
A familial polymorphic variant of chromosome 5
- PMID: 6162934
- PMCID: PMC1885919
- DOI: 10.1136/jmg.17.6.444
Item in Clipboard
Case Reports
A familial polymorphic variant of chromosome 5
J Med Genet.
1980 Dec.
Abstract
Two male fetuses and their mothers, referred for amniocentesis because of high levels of AFP in their blood, were found to carry an anomalous chromosome 5 with a large heterochromatic segment in the long arm. One of the fetuses had an additional ring chromosome.
Similar articles
-
A simple procedure for obtaining fetal chromosome preparations from bloodstained amniotic fluid.Prenat Diagn. 1982 Apr;2(2):139-41. doi: 10.1002/pd.1970020211. Prenat Diagn. 1982. PMID: 6183655 No abstract available.
-
Risk of fetal chromosomal anomalies in patients with elevated maternal serum alpha-fetoprotein.Obstet Gynecol. 1990 Jan;75(1):64-6. Obstet Gynecol. 1990. PMID: 1688649
-
[Biochemical analysis of the amniotic fluid in early amniocentesis. Importance of alpha-fetoproteins].Minerva Ginecol. 1980 Jun;32(6):539-44. Minerva Ginecol. 1980. PMID: 6165937 Italian. No abstract available.
-
Characterization of a small supernumerary marker chromosome as r(8) at prenatal diagnosis by MFISH.Prenat Diagn. 2005 Jan;25(1):73-8. doi: 10.1002/pd.1087. Prenat Diagn. 2005. PMID: 15662692 Review.
-
Antenatal diagnosis of genetic disease.Ann Clin Lab Sci. 1975 May-Jun;5(3):153-60. Ann Clin Lab Sci. 1975. PMID: 49167 Review.
Cited by
-
Aspects of evaluation, significance, and evolution of human C-band heteromorphism.Hum Genet. 1982;61(4):281-94. doi: 10.1007/BF00276592. Hum Genet. 1982. PMID: 6759365 Review.
-
Centromeric alpha satellite DNA amplification and translocation in an unusually large chromosome 14p+ variant.Hum Genet. 1989 May;82(2):154-8. doi: 10.1007/BF00284049. Hum Genet. 1989. PMID: 2722191
-
A new variant of chromosome 3 with unusual staining properties.J Med Genet. 1988 Nov;25(11):781-2. doi: 10.1136/jmg.25.11.781. J Med Genet. 1988. PMID: 2467000 Free PMC article. No abstract available.
-
A rare chromosome 5 heterochromatic variant derived from insertion of 9qh satellite 3 sequences.Chromosome Res. 1998 Aug;6(5):411-4. doi: 10.1023/a:1009237608514. Chromosome Res. 1998. PMID: 9872671
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
