Literature DB >> 5314293

A case of 18q- in a t(18q-;6p+) family.

P Jacobsen, M Mikkelsen, E Niebuhr, J de Grouchy.   

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Year:  1971        PMID： 5314293

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


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  6 in total

1.  The cytogenetics of 90 patients with idiopathic mental retardation/malformation syndromes and of 90 normal subjects.

Authors:  C T Doyle
Journal:  Hum Genet       Date:  1976-07-27       Impact factor: 4.132

Review 2.  [Ring chromosome 18. 18p-/18q- -deletion-syndrome].

Authors:  J Kunze; E Stephan; M Tolksdorf
Journal:  Humangenetik       Date:  1972

Review 3.  Partial monosomies 18. Review of cytogenetical and phenotypical variants.

Authors:  I W Lurie; G I Lazjuk
Journal:  Humangenetik       Date:  1972

4.  A case of 18q-in a family with a translocation t(6p+;18q-), identified by the Giemsa-banding technique.

Authors:  W L Gouw; L P ten Kate; G J Anders; A Okken
Journal:  Humangenetik       Date:  1973

5.  Familial mental retardation in a family with an inherited chromosome rearrangement.

Authors:  A E Chudley; F Bauder; M Ray; P J McAlpine; S D Pena; J L Hamerton
Journal:  J Med Genet       Date:  1974-12       Impact factor: 6.318

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

Authors:  A Schinzel; K Hayashi; W Schmid
Journal:  Humangenetik       Date:  1975
  6 in total

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