Literature DB >> 302681

[Ring of the chromosome 4. I - With 4p- phenotype].

J Fraisse, B Lauras, J Couturier, F Freycon.   

Abstract

A ring chromosome derived from a No. 4 chromosome was found in the complement of an 8-year-old boy with mental retardation and growth retardation and developmental defects characteristic of 4p deletion. Break points were at 4p15 and 4q35.

Entities:  

Mesh：

Year:  1977        PMID： 302681

Source DB:  PubMed          Journal:  Ann Genet        ISSN： 0003-3995


  4 in total

1.  Partial deletion of 4p16 band in a ring chromosome and Wolf Syndrome.

Authors:  J del Mazo; J A Abrisqueta; A Pérez-Castillo; V Aller; M A Lucas; M L de Torres; M J Martín
Journal:  Hum Genet       Date:  1978-10-19       Impact factor: 4.132

2.  Familial ring (20) chromosomal mosaicism.

Authors:  E Back; I Voiculescu; M Brünger; G Wolff
Journal:  Hum Genet       Date:  1989-09       Impact factor: 4.132

3.  Genetic and clinical studies in 13 patients with the Wolf-Hirschhorn syndrome [del(4p)].

Authors:  M G Wilson; J W Towner; G S Coffin; A J Ebbin; E Siris; P Brager
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

4.  Clinical, cytogenetic, and molecular findings in a patient with ring chromosome 4: case report and literature review.

Authors:  César Paz-Y-Miño; Ana Proaño; Stella D Verdezoto; Juan Luis García; Jesús María Hernández-Rivas; Paola E Leone
Journal:  BMC Med Genomics       Date:  2019-11-21       Impact factor: 3.063
  4 in total

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