Isolation of chromosome-21-specific DNA probes and their use in the analysis of nondisjunction in Down syndrome-Reference-Cited by-同舟云学术

Isolation of chromosome-21-specific DNA probes and their use in the analysis of nondisjunction in Down syndrome

Published:1989-01 Issue:2 Volume:81 Page:113-119
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Galt J.,Boyd E.,Connor J. M.,Ferguson-Smith M. A.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00293885.pdf

Reference31 articles.

1. Antonarakis SE, Chakravati A, Warren AC, Slaugenhaupt SA, Wong C, Halloran SL, Metaxotou C (1986) Reduced recombination rate on chromosomes 21 that have undergone nondisjunction. Cold Spring Harbor Symp Quant Biol 51:158?190

2. Ayme S, Baccicheti C, Bricarelli FD, Dallapiccola B, Lungarotti D, Mikkelsen M, Nevin N (1986) Factors involved in chromosomal nondisjunction: a European collaborative study, supported by the EEC. 7th International Congress of Human Genetics, Berlin 1986, part I: CIV. 19 (abstr)

3. Bradley CM, Patterson D, Robinson A (1986) Somatic cell genetic studies on the family with Down syndrome due to an unusual translocation (21q22-21qter). Trisomy 21 1:41?52

4. Carothers A (1987) Down syndrome and maternal age: the effect of erroneous assignment of parental origin. Am J Hum Genet 40:147?150

5. Carpenter NJ, Mayes JS, Say B, Wilson DP (1987) Partial deletion 21: case report with biochemical studies and review. J Med Genet 24:706?709

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