The 18q- syndrome: analysis of chromosomes by bivariate flow karyotyping and the PCR reveals a successive set of deletion breakpoints within 18q21.2-q22.2. (Q35643390)

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scientific article published on April 1995

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English	The 18q- syndrome: analysis of chromosomes by bivariate flow karyotyping and the PCR reveals a successive set of deletion breakpoints within 18q21.2-q22.2.	scientific article published on April 1995

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scholarly article

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24 October 2019

The 18q- syndrome: analysis of chromosomes by bivariate flow karyotyping and the PCR reveals a successive set of deletion breakpoints within 18q21.2-q22.2. (English)

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G A Silverman

1

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S S Schneider

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H F Massa

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A Flint

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M Lalande

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J C Leonard

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J Overhauser

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G van den Engh

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B J Trask

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1 April 1995

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American Journal of Human Genetics

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56

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926-937

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4

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24 October 2019

Molecular analysis of the 18q- syndrome--and correlation with phenotype.

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Chromosomal reassignment: YACs containing both YES1 and thymidylate synthase map to the short arm of chromosome 18

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Interstitial deletions are not the main mechanism leading to 18q deletions

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Immunological profile in a chromosome 18 deletion syndrome with IgA deficiency

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Neurologic manifestations in 18q- syndrome

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Structural aberrations of chromosome 18. II. The 18q- syndrome. Report of three cases

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PARTIAL DELETION OF THE LONG ARMS OF THE CHROMOSOME 18

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Partial deletion of the long arm of chromosome 18. Individualization of a new morbid state

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[Deletion of the long arm of chromosome 18, primary hypothyroidism, Biermer's anemia and IgM hypogammaglobulinemia]

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The Effect of the Shiverer Mutation on Myelin Basic Protein Expression in Homozygous and Heterozygous Mouse Brain

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Identifiers

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24 October 2019

1 reference

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24 October 2019

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