On the localization of genes on certain autosomes of man through chromosome aberrations

Bender, Klaus; Burckhardt, K.

doi:10.1007/bf00696016

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Analysis Of Genetic Markers1

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1970

1979

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Cited by 7 publications

(1 citation statement)

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“…Conversely, the following genes will not be situated on the missing segment: MN, Hp, ac.P. ; Kidd, GPT, HL-A, Gc, Pt (for a discussion of the possibilities and restrictions of the localization exclusion method see Bender & Burckhardt 1970)).…”

Section: Analysis Of Genetic Markersmentioning

confidence: 99%

A case with 46, XX, del (11) (q21)

Faust

Vogel²,

B³

1974

Clinical Genetics

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The cytogenetic analysis of a child with unspecific dysplastic signs revealed the karyotype: 46, XX, del(11) (q21). Two hypotheses could explain the mild phenotypical expression of this deletion: 1) The material of the deficient part of chromosome 11 is genetically inert or redundant (which seems unlikely); 2) “Gene‐dosis‐compensation” occurs for the loss of genes on the deficient part of chromosome 11.

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Section: Analysis Of Genetic Markersmentioning

confidence: 99%