» Articles » PMID: 6210618

Maternally Transmitted Extra Ring (21) Chromosome in a Boy with Down's Syndrome

Overview
Journal Hum Genet
Specialty Genetics
Date 1982 Jan 1
PMID 6210618
Citations 5
Authors
Affiliations
Soon will be listed here.
Citing Articles

Segregation of a 22 ring chromosome in three generations.

Stoll C, Roth M Hum Genet. 1983; 63(3):294-6.

PMID: 6852827 DOI: 10.1007/BF00284669.


Prenatal detection of an unstable ring 21 chromosome.

Stetten G, Sroka B, Corson V, Boehm C Hum Genet. 1984; 68(4):310-3.

PMID: 6510909 DOI: 10.1007/BF00292590.


Ring chromosome 21 in healthy persons: different consequences in females and in males.

Dallapiccola B, De Filippis V, Notarangelo A, Perla G, Zelante L Hum Genet. 1986; 73(3):218-20.

PMID: 3733078 DOI: 10.1007/BF00401230.


Molecular mechanism in the formation of a human ring chromosome 21.

Wong C, Kazazian Jr H, Stetten G, Earnshaw W, Van Keuren M, Antonarakis S Proc Natl Acad Sci U S A. 1989; 86(6):1914-8.

PMID: 2648387 PMC: 286815. DOI: 10.1073/pnas.86.6.1914.


Inherited ring chromosomes: an analysis of published cases.

Kosztolanyi G, Mehes K, Hook E Hum Genet. 1991; 87(3):320-4.

PMID: 1864607 DOI: 10.1007/BF00200912.

References
1.
Leschot N, Slater R, Joenje H, De Nef J . SOD-A and chromosome 21. Conflicting findings in a familial translocation (9p24;21q214). Hum Genet. 1981; 57(2):220-3. DOI: 10.1007/BF00282029. View

2.
Palmer C, Hodes M, Reed T, Kojetin J . Four new cases of ring 21 and 22 including familial transmission of ring 21. J Med Genet. 1977; 14(1):54-60. PMC: 1013508. DOI: 10.1136/jmg.14.1.54. View

3.
CROSTI N, Serra A, Rigo A, Viglino P . Dosage effect of SOD-A gene in 21-trisomic cells. Hum Genet. 1976; 31(2):197-202. DOI: 10.1007/BF00296146. View

4.
Bloom S, Goodpasture C . An improved technique for selective silver staining of nucleolar organizer regions in human chromosomes. Hum Genet. 1976; 34(2):199-206. DOI: 10.1007/BF00278889. View

5.
Hagemeijer A, Smit E . Partial trisomy 21. Further evidence that trisomy of band 21q22 is essential for Down's phenotype. Hum Genet. 1977; 38(1):15-23. DOI: 10.1007/BF00295803. View