Literature DB >> 5301688

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

A Valdmanis, G Pearson, A E Siegel, R H Hoeksema, J D Mann.   

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Year:  1967        PMID: 5301688

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


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  15 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

Review 4.  Malformations of kidney and urinary tract in common chromosomal aberrations. II. Morphogenetic studies.

Authors:  G Töndury
Journal:  Humangenetik       Date:  1973-03-23

5.  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

6.  Trisomy-18 syndrome caused by translocation or isochromosome formation. A case report with bibliography.

Authors:  H Müller; E M Bühler; E Signer; F Egli; G R Stalder
Journal:  J Med Genet       Date:  1972-12       Impact factor: 6.318

7.  [Partial trisomy for the short arm of chromosome 4 with translocation 4p-,18q+ in the father].

Authors:  A Schinzel; W Schmid
Journal:  Humangenetik       Date:  1972

8.  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

9.  [Multiple abnormalities in a girl with a 46, XY,17q+ karyotype].

Authors:  W Engel; H Reinwein; D Bombel; H Ritter; U Wolf
Journal:  Humangenetik       Date:  1968

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

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