Literature DB >> 6463029

A rare non-heterochromatic 9p+ variant in two amniotic fluid cell cultures.

N Archidiacono, V Pecile, M Rocchi, L Dalpra, G Nocera, G Simoni.   

Abstract

Mesh：

Year:  1984        PMID： 6463029     DOI： 10.1002/pd.1970040313

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN： 0197-3851            Impact factor:   3.050


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  6 in total

Review 1.  Chromosome imbalance, normal phenotype, and imprinting.

Authors:  L Bortotto; E Piovan; R Furlan; H Rivera; O Zuffardi
Journal:  J Med Genet       Date:  1990-09       Impact factor: 6.318

2.  The euchromatic 9p+ polymorphism is a locus-specific amplification caused by repeated copies of a small DNA segment mapping within 9p12.

Authors:  Rosetta Lecce; Marina Murdolo; Gianfranco Gelli; Katharina Steindl; Livia Coppola; Anna Romano; Elisa Cupelli; Giovanni Neri; Marcella Zollino
Journal:  Hum Genet       Date:  2005-12-02       Impact factor: 4.132

3.  Replication studies in the 16p+ variant.

Authors:  P W Thompson; S H Roberts; S M Rees
Journal:  Hum Genet       Date:  1990-03       Impact factor: 4.132

4.  Non C-banding variants in some normal families might be homogeneously staining regions.

Authors:  G C Webb; E J Krumins; S Z Eichenbaum; L E Voullaire; E Earle; K H Choó
Journal:  Hum Genet       Date:  1989-04       Impact factor: 4.132

5.  A new variant of chromosome 16.

Authors:  P W Thompson; S H Roberts
Journal:  Hum Genet       Date:  1987-05       Impact factor: 4.132

Review 6.  Directly transmitted unbalanced chromosome abnormalities and euchromatic variants.

Authors:  J C K Barber
Journal:  J Med Genet       Date:  2005-08       Impact factor: 6.318
  6 in total

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