Literature DB >> 2918531

Duplication 6p and deletion 9p.

C Lytle1, J Wade, A Farrier, F Flohrschutz, B Hecht, J Allanson.   

Abstract

Mesh：

Year:  1989        PMID： 2918531      PMCID： PMC1015543          DOI： 10.1136/jmg.26.1.64

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  4 in total

1.  A family with a presumptive C-F translocation in five generations.

Authors:  A J Therkelsen; T Klinge; K Henningsen; M Mikkelsen; G Schmidt
Journal:  Ann Genet       Date:  1971-03

2.  Hereditary 3;6 translocation : three cases of multiple malformations with partial trisomy 6p21 leads to pter.

Authors:  L Pagano; G Fioretti; M Vetrella; E Risolo; C Casullo; A Celona; S Renda; A Rinaldi; V Ventruto
Journal:  Ann Genet       Date:  1980

3.  Partial trisomy 6p: 46,XX, -10, der(10),t(6;10) (p22;q26)pat and HLA localisation.

Authors:  P Ferrando; C San Román; S Rodriguez de Cordoba; A Arnaiz-Villena
Journal:  J Med Genet       Date:  1981-06       Impact factor: 6.318

4.  Trisomy 6p22 leads to 6pter due to familial t(6;13)(p22;q34 or 33) translocation.

Authors:  G Rosi; G Venti; G Migliorini Brushelli; E Donti; V Bocchini; R Armellini
Journal:  Hum Genet       Date:  1979-09-02       Impact factor: 4.132
  4 in total
  1 in total

1.  Diagnostic Approach to Microdeletion Syndromes Based on 22q11.2 Investigation: Challenges in Four Cases.

Authors:  Ilária C Sgardioli; Matheus de Mello Copelli; Fabíola P Monteiro; Ana P Dos Santos; Elaine Lustosa Mendes; Társis Paiva Vieira; Vera L Gil-da-Silva-Lopes
Journal:  Mol Syndromol       Date:  2017-06-24
  1 in total

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