Literature DB >> 870409

Partial trisomy of the long arm of human chromosome 1 as demostrated by in situ hybridization with 5S ribosomal RNA.

D M Steffensen, E H Chu, D P Speert, P M Wall, K Meilinger, R P Kelch.   

Abstract

In a newborn boy with multiple malformations, a tandem duplication was detected at the distal end of the long arm of one human chromosome 1. The Giemsa bands, 1q31 to 1q43--44, were repeated serially. Since 5S rRNA genes are located at 1q42--43, in situ hybridization of 125I 5S rRNA with fixed chromosome preparations was used to confirm the chromosomal duplication. The infant exhibited numerous developmental and clinical abnormalities as might be expected with an abnormality of chromosome structure relating to a ribosome component.

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Year:  1977        PMID: 870409     DOI: 10.1007/bf00390432

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  14 in total

1.  The site of 5S RNA genes in human chromosome 1.

Authors:  K C Atwood; M T Yu; L D Johnson; A S Henderson
Journal:  Cytogenet Cell Genet       Date:  1975

2.  Cytogenetic studies in polycythemia vera.

Authors:  D Wurster-Hill; J Whang-Peng; O R McIntyre; L Y Hsu; K Hirschhorn; B Modan; A V Pisciotta; R Pierre; S P Balcerzak; S Murphy; A Weinfeld
Journal:  Semin Hematol       Date:  1976-01       Impact factor: 3.851

3.  Human gene mapping. 2. Rotterdam Conference (1974). 2d International Workshop on Human Gene Mapping. Report of the committee on the genetic constitution of chromosomes 1 and 2.

Authors: 
Journal:  Cytogenet Cell Genet       Date:  1975

4.  Mapping the human 5S RNA genes on chromosome 1 using translocations.

Authors:  D M Steffensen; W Prensky; D Mutton; J L Hamerton
Journal:  Cytogenet Cell Genet       Date:  1975

5.  Localisation of 5S ribosomal RNA genes on human chromosome 1.

Authors:  D M Steffensen; P Duffey; W Prensky
Journal:  Nature       Date:  1974-12-20       Impact factor: 49.962

6.  The use of iodinated RNA for gene localization.

Authors:  W Prensky; D M Steffensen; W L Hughes
Journal:  Proc Natl Acad Sci U S A       Date:  1973-06       Impact factor: 11.205

7.  A "Philadelphia-like" chromosome derived from the Y in a patient with refractory dysplastic anemia.

Authors:  D Warburton; A Bluming
Journal:  Blood       Date:  1973-11       Impact factor: 22.113

8.  Identification of normal and abnormal chromosomes in tumor cells.

Authors:  L Tiepolo; O Zuffardi
Journal:  Cytogenet Cell Genet       Date:  1973

9.  Studies of fractionated HeLa cell metaphase chromosomes. II. chromosomal distribution of sites for transfer RNA and 5 s RNA.

Authors:  Y Aloni; L E Hatlen; G Attardi
Journal:  J Mol Biol       Date:  1971-03-28       Impact factor: 5.469

10.  Abnormalities of chromosome 1 in myeloproliferative disorders.

Authors:  J D Rowley
Journal:  Cancer       Date:  1975-11       Impact factor: 6.860

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  18 in total

1.  Detection of a de novo duplication of 1q32-qter by fluorescence in situ hybridisation in a boy with multiple malformations: further delineation of the trisomy 1q syndrome.

Authors:  H C Duba; M Erdel; J Löffler; L Bereuther; H Fischer; B Utermann; G Utermann
Journal:  J Med Genet       Date:  1997-04       Impact factor: 6.318

2.  Genomewide linkage scan for split-hand/foot malformation with long-bone deficiency in a large Arab family identifies two novel susceptibility loci on chromosomes 1q42.2-q43 and 6q14.1.

Authors:  Mohammed Naveed; Swapan K Nath; Mathew Gaines; Mahmoud T Al-Ali; Najib Al-Khaja; David Hutchings; Jeffrey Golla; Samuel Deutsch; Armand Bottani; Stylianos E Antonarakis; Uppala Ratnamala; Uppala Radhakrishna
Journal:  Am J Hum Genet       Date:  2006-11-29       Impact factor: 11.025

3.  Micro-duplications of 1q32.1 associated with neurodevelopmental delay.

Authors:  H E Olson; Y Shen; A Poduri; M P Gorman; K A Dies; M Robbins; R Hundley; B Wu; M Sahin
Journal:  Eur J Med Genet       Date:  2012-01-02       Impact factor: 2.708

4.  Tandem duplication (5q13 to 22) in a mentally deficient girl.

Authors:  E Kessel; R A Pfeiffer
Journal:  Hum Genet       Date:  1979-11       Impact factor: 4.132

5.  Omphalocele and partial trisomy 1q syndrome.

Authors:  H Chen; J J Gershanik; J B Mailhes; I D Sanusi
Journal:  Hum Genet       Date:  1979       Impact factor: 4.132

6.  Partial trisomy of the long arm of chromosome 1 due to a familial translocation t(1;10) (q32;q26).

Authors:  A Bonfante; M Stella; G Rossi
Journal:  Hum Genet       Date:  1978-12-29       Impact factor: 4.132

7.  Duplication-deletion with partial trisomy lq and partial monosomy 3p resulting from a maternal reciprocal translocation rcp (1;3) (q32;p25).

Authors:  A Schinzel
Journal:  J Med Genet       Date:  1981-02       Impact factor: 6.318

8.  Terminal deletion of the long arm of chromosome 1 in a malformed newborn.

Authors:  E Kessel; R A Pfeiffer; W Blanke; J Schwarz
Journal:  Hum Genet       Date:  1978-06-27       Impact factor: 4.132

9.  Partial trisomy of chromosome no. 1 in two adult brothers due to maternal translocation (1q--;6p+).

Authors:  K Taysi; G S Sekhon
Journal:  Hum Genet       Date:  1978-11-16       Impact factor: 4.132

10.  Proteinuric glomerulopathy in an adolescent with a distal partial trisomy chromosome 1.

Authors:  Takaya Sasaki; Masahiro Okabe; Takeshi Tosaki; Yu Honda; Masahiro Ishikawa; Nobuo Tsuboi; Takashi Yokoo
Journal:  CEN Case Rep       Date:  2018-05-16
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