Literature DB >> 4725908

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

W L Gouw, L P ten Kate, G J Anders, A Okken.   

Abstract

Mesh：

Year:  1973        PMID： 4725908     DOI： 10.1007/BF00295240

Source DB:  PubMed          Journal:  Humangenetik        ISSN： 0018-7348


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  6 in total

1.  [PARTIAL DELETION OF THE LONG ARMS OF THE CHROMOSOME 18].

Authors:  J DE GROUCHY; P ROYER; C SALMON; M LAMY
Journal:  Pathol Biol       Date:  1964-05

2.  New technique for distinguishing between human chromosomes.

Authors:  A T Sumner; H J Evans; R A Buckland
Journal:  Nat New Biol       Date:  1971-07-07

3.  Gene deletion and duplication effects on phenotype and gamma globulin levels.

Authors:  N L Rudd; P H Lamarche
Journal:  J Med Genet       Date:  1971-03       Impact factor: 6.318

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

Authors:  P Jacobsen; M Mikkelsen; E Niebuhr; J de Grouchy
Journal:  Ann Genet       Date:  1971-03

5.  Familial 18 q- syndrome.

Authors:  E M Law; J G Masterson
Journal:  Ann Genet       Date:  1969-12

6.  A pedigree of 4/18 translocation chromosomes with type and countertype partial trisomy and partal monosomy for chromosome 18.

Authors:  A Valdmanis; G Pearson; A E Siegel; R H Hoeksema; J D Mann
Journal:  Ann Genet       Date:  1967-12
  6 in total
  4 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

2.  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

3.  Partial trisomy 6p with karyotype 46,XY,der(22), t(6;22)(p22;q13)mat.

Authors:  G B Côté; S Papadakou-Lagoyanni; S Sbyrakis
Journal:  J Med Genet       Date:  1978-12       Impact factor: 6.318

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

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

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