Literature DB >> 10528239

Proximal 5p trisomy resulting from a marker chromosome implicates band 5p13 in 5p trisomy syndrome.

J R Avansino1, T R Dennis, P Spallone, A D Stock, M L Levin.   

Abstract

We describe an infant with trisomy of (5)(p10p13.1) resulting from a de novo marker chromosome. The marker's origin was identified by chromosome microdissection and reverse in situ hybridization. The clinical findings are compared to those of other partial and complete 5p duplications. This case further defines the critical region of 5p trisomy syndrome to proximal 5p. Copyright 1999 Wiley-Liss, Inc.

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Year:  1999        PMID: 10528239

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  8 in total

1.  Partial 5p monosomy or trisomy in 11 patients from a family with a t(5;15)(p13.3;p12) translocation.

Authors:  Acácia Fernandes Lacerda de Carvalho; Fernanda Teixeira da Silva Bellucco; Leslie Domenici Kulikowski; Maria Betânia Pereira Toralles; Maria Isabel Melaragno
Journal:  Hum Genet       Date:  2008-09-07       Impact factor: 4.132

Review 2.  Chromosome 5 derived small supernumerary marker: towards a genotype/phenotype correlation of proximal chromosome 5 imbalances.

Authors:  Joana Barbosa Melo; Liesbeth Backx; Joris R Vermeesch; Heloisa G Santos; Ana C Sousa; Nadezda Kosyakova; Anja Weise; Ferdinand von Eggeling; Thomas Liehr; Isabel Marques Carreira
Journal:  J Appl Genet       Date:  2011-03-25       Impact factor: 3.240

3.  Electroclinical characteristics and neuropsychological profile of a female child with chromosome 5p13.2 duplication syndrome.

Authors:  Elisabetta Lucarelli; Maria Grazia Pasca; Isabella Fanizza; Antonio Trabacca
Journal:  Neurol Sci       Date:  2017-01-20       Impact factor: 3.307

4.  Novel phenotype of 5p13.3-q11.2 duplication resulting from supernumerary marker chromosome 5: implications for management and genetic counseling.

Authors:  Margaret E Armstrong; David D Weaver; Melissa D Lah; Gail H Vance; Benjamin J Landis; Stephanie M Ware; Benjamin M Helm
Journal:  Mol Cytogenet       Date:  2018-03-27       Impact factor: 2.009

5.  Trisomy 5p with bilateral congenital diaphragmatic hernia: a case report.

Authors:  Noriyuki Nakamura; Takafumi Ushida; Yoshinori Moriyama; Kenji Imai; Tomoko Nakano-Kobayashi; Satoko Osuka; Maki Goto; Hiroaki Kajiyama; Hideyuki Asada; Masahiro Hayakawa; Tomomi Kotani
Journal:  J Med Case Rep       Date:  2021-03-10

6.  A novel unbalanced translocation between chromosomes 5p and 18q leading to dysmorphology and global developmental delay.

Authors:  Giavanna Verdi; Dong Li; Sarah H Elsea; Beverly Nelson; Elizabeth J Bhoj; Hakon Hakonarson; Katherine R Yearwood; Sharmila Upadhya; Sarah Gluschitz; Janice L Smith; Andrew K Sobering
Journal:  Mol Genet Genomic Med       Date:  2022-02-21       Impact factor: 2.183

7.  First case of two supernumerary markers derived from chromosome 5 and chromosome 8.

Authors:  Roberta Giansante; Chiara Palka Bayard De Volo; Melissa Alfonsi; Elisena Morizio; Paolo Guanciali Franchi
Journal:  Mol Cytogenet       Date:  2022-06-27       Impact factor: 1.904

8.  A coalescence of two syndromes in a girl with terminal deletion and inverted duplication of chromosome 5.

Authors:  Danijela Krgovic; Ana Blatnik; Ante Burmas; Andreja Zagorac; Nadja Kokalj Vokac
Journal:  BMC Med Genet       Date:  2014-02-11       Impact factor: 2.103

  8 in total

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