Literature DB >> 657850

Deletion in the long arm of chromosome 1 from a subject with multiple congenital anomalies. Respository identification No. GM-2025.

G S Sekhon, R E Hillman, R Yu, M M Aronson, A E Greene, L L Coriell.   

Abstract

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Year:  1978        PMID： 657850     DOI： 10.1159/000130894

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN： 0301-0171


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  4 in total

1.  Mild phenotype associated with an interstitial deletion of the long arm of chromosome 1.

Authors:  D Melis; L Perone; M P Sperandeo; M S Sabbatino; M R Tuzzi; A Romano; G Parenti; G Andria
Journal:  J Med Genet       Date:  1998-12       Impact factor: 6.318

2.  A new case of interstitial 1q 25.3-32.1 deletion: cytogenetic analysis molecular characterization and ultrasound findings.

Authors:  Francesco Libotte; Domenico Bizzoco; Ivan Gabrielli; Caterina Tamburrino; Cristina Ernandez; Lorena Carpineto; Maria Pia D'Aleo; Antonella Cima; Alvaro Mesoraca; Pietro Cignini; Alessia Aloisi; Roberto Angioli; Salvatore Giovanni Vitale; Claudio Giorlandino
Journal:  J Prenat Med       Date:  2015 Jan-Jun

3.  Interstitial deletion in the long arms of chromosome 1: 46,XY,del(1)(pter leads to q22::q25 leads to qter).

Authors:  C E de Pablo; J M García Sagredo; M T Ferro; P Ferrando; C San Román
Journal:  J Med Genet       Date:  1980-12       Impact factor: 6.318

4.  Prenatal diagnosis of a rare de novo 1q22-q25.1 chromosomal deletion syndrome using oligo array CGH.

Authors:  Gholamreza Shariati; Alihossein Saberi; Mohammad Hamid; Hamid Galehdari; Alireza Sedaghat; Nehzat Abdorasuli
Journal:  Clin Case Rep       Date:  2018-06-13
  4 in total

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