Karyotype–phenotype analysis and molecular delineation of a 3p26 deletion/8q24.3 duplication case with a virtually normal phenotype and mild cognitive deficit-Reference-Cited by-同舟云学术

Karyotype–phenotype analysis and molecular delineation of a 3p26 deletion/8q24.3 duplication case with a virtually normal phenotype and mild cognitive deficit

Published:2006-02-15 Issue:4 Volume:140A Page:388-391
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Shrimpton Antony E.,Jensen Kimberly A.,Hoo Joe J.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference16 articles.

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2. . 1984. Clinical Atlas of Human Chromosomes. Second Edition. New York: John Wiley & Sons.

3. Precise localisation of 3p25 breakpoints in four patients with the 3p-syndrome.

4. An unbalanced submicroscopic translocation t(8;16)(q24.3;p13.3)pat associated with tuberous sclerosis complex, adult polycystic kidney disease, and hypomelanosis of Ito

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