Literature DB >> 5296303

[Deletion of the short arm of a 13-15 chromosome, hypertelorism and Hp0 haptoglobin phenotype in the same family].

J de Grouchy, C Salmon, D Salmon, P Maroteaux.   

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Year:  1966        PMID： 5296303

Source DB:  PubMed          Journal:  Ann Genet        ISSN： 0003-3995


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  6 in total

1.  Familial short arm deletion of chromosome no. 15.

Authors:  J J Hoo; U Hillig; H Cramer; S Hansen; F Hermann
Journal:  Humangenetik       Date:  1974

2.  Frequency of deletion of short arm satellites in acrocentric chromosomes.

Authors:  J Nielsen; U Friedrich; A B Hreidarsson
Journal:  J Med Genet       Date:  1974-06       Impact factor: 6.318

Review 3.  [On the problem of assigning genes to definite human autosomes with the aid of chromosome aberrations].

Authors:  K Bender; H Ritter; U Wolf
Journal:  Humangenetik       Date:  1967

4.  Short arm deletion of chromosome 14.

Authors:  I Emerit; B Noel; M Thiriet; M Loubon; B Quack
Journal:  Humangenetik       Date:  1972

5.  Retinoblastoma and deletion D (14) syndrome.

Authors:  M G Wilson; J Melnyk; J W Towner
Journal:  J Med Genet       Date:  1969-09       Impact factor: 6.318

6.  On the localization of genes on certain autosomes of man through chromosome aberrations. 3. Exclusion of the possibility of gene assignment.

Authors:  K Bender; K Burckhardt
Journal:  Humangenetik       Date:  1970
  6 in total

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