Literature DB >> 129308

Inherited t2q-/15q+ translocation and Down's syndrome.

C Stoll, J J Kuss, E Schneegans.   

Abstract

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Year:  1976        PMID： 129308     DOI： 10.1111/j.1399-0004.1976.tb01542.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  6 in total

1.  Familial balanced translocation 4p+/17q- as a suggested cause of primary trisomy-21 Down's syndrome.

Authors:  K Oikawa; M Trent; R Lebovitz
Journal:  Arch Dis Child       Date:  1977-11       Impact factor: 3.791

2.  Down's syndrome with XYY additional aneuploidy.

Authors:  C Stoll; D Frey; D Willard; J Messer
Journal:  Hum Genet       Date:  1976-09-10       Impact factor: 4.132

3.  Sister chromatid exchanges in balanced translocation carriers and in patients with unbalanced karyotypes.

Authors:  C Stoll; D S Borgaonkar; P Bigel
Journal:  Hum Genet       Date:  1977-06-10       Impact factor: 4.132

4.  Trisomy 21 Down syndrome. II. Structural chromosome rearrangements in the parents.

Authors:  I A Uchida; V C Freeman
Journal:  Hum Genet       Date:  1986-02       Impact factor: 4.132

5.  Nonrandom distribution of exchange points in patients with reciprocal translocations.

Authors:  C Stoll
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

Review 6.  Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysis.

Authors:  M G Mattei; N Souiah; J F Mattei
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132
  6 in total

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