Literature DB >> 688692

Abnormalities resulting from a familial pericentric inversion of chromosome 18.

M K Kukolich, B W Althaus, J W Sears, C B Mankinen, R C Lewandowski.   

Abstract

Mesh：

Year:  1978        PMID： 688692     DOI： 10.1111/j.1399-0004.1978.tb02113.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  4 in total

1.  A Peruvian Child with 18p-/18q+ Syndrome and Persistent Microscopic Hematuria.

Authors:  Julio A Poterico; Flor Vásquez; Miguel Chávez-Pastor; Milana Trubnykova; Félix Chavesta; Jenny Chirinos; Nancy Salcedo; Rosmery Mena; Sulema Cubas; Rocío González; Rossana Alvariño; Hugo Abarca-Barriga
Journal:  J Pediatr Genet       Date:  2017-07-06

2.  Duplication-deficiency of chromosome 18, resulting from recombination of a paternal pericentric invesion, with a note for genetic counselling.

Authors:  J R Teyssier; F Bajolle
Journal:  Hum Genet       Date:  1980-02       Impact factor: 4.132

3.  Pericentric inversion of chromosome 18 in parents leading to a phenotypically normal child with segmental uniparental disomy 18.

Authors:  Ariana Kariminejad; Roxana Kariminejad; Azadeh Moshtagh; Maryam Zanganeh; Mohammad Hassan Kariminejad; Stefan Neuenschwander; Michal Okoniewski; Eva Wey; Albert Schinzel; Alessandra Baumer
Journal:  Eur J Hum Genet       Date:  2011-02-16       Impact factor: 4.246

Review 4.  Pericentric inversions. Problems and significance for clinical genetics.

Authors:  P Kaiser
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132
  4 in total

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