Literature DB >> 6716413

Trisomy 1q24----1q41 in two sibs with an insertion in an inverted chromosome 4.

C Stoll, M P Roth, B Dott.   

Abstract

We report two patients whose karyotype revealed an additional segment 1q inserted into an inverted chromosome 4. The patients were partially trisomic for the region 1q24----1q41, karyotype 46,XY or XX, inv ins(4;1)inv(4)(q28;q24q41)(p15 . 3q28), while in the mother the chromosomal aberration was balanced. The inserted segment was inverted. In six patients from three other families with insertions, the segment 1q25----1q32 was inserted into the short arm of chromosome 1. In another patient, the segment 1q25----1q42 of the mother was inverted and inserted into the long arm of chromosome 6. These findings suggest an increased susceptibility for a segment of the long arm of chromosome 1 to be inserted and inverted in rearrangements.

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Year:  1984        PMID: 6716413      PMCID: PMC1049243          DOI: 10.1136/jmg.21.2.133

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  7 in total

1.  Partial monosomy or trisomy resulting from crossing over within a rearranged chromosome 1.

Authors:  K L Garver; A M Ciocco; N A Turack
Journal:  Clin Genet       Date:  1976-12       Impact factor: 4.438

2.  Partial trisomy 1 due to a "shift" and probable location of the Duffy (Fy) locus.

Authors:  C G Palmer; J C Christian; A D Merritt
Journal:  Am J Hum Genet       Date:  1977-07       Impact factor: 11.025

3.  Possible trisomy 1q25 leads to 1q32 in a malformed girl with a de novo insertion in 1q.

Authors:  A Schinzel
Journal:  Hum Genet       Date:  1979-06-19       Impact factor: 4.132

4.  Partial trisomy of chromosome 1 resulting from a complex maternal rearrangement of chromosomes 1, 5, and 6.

Authors:  T W Hustinx; F A Nabben; J M Scheres
Journal:  Am J Med Genet       Date:  1979

5.  Meiotic consequences of an intrachromosomal insertion of chromosome No 1: a family pedigree.

Authors:  S F Pan; S R Fatora; R Sorg; K L Garver; M W Steele
Journal:  Clin Genet       Date:  1977-11       Impact factor: 4.438

Review 6.  The Cri du Chat syndrome: epidemiology, cytogenetics, and clinical features.

Authors:  E Niebuhr
Journal:  Hum Genet       Date:  1978-11-16       Impact factor: 4.132

7.  De novo duplication 1q32-q42: variability of phenotypic features in partial lq trisomics.

Authors:  M S Lungarotti; A Falorni; A Calabro; F Passalacqua; B Dallapiccola
Journal:  J Med Genet       Date:  1980-10       Impact factor: 6.318

  7 in total

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