Literature DB >> 6694184

Balanced rearrangements of the autosomes: results of a longitudinal study of a newborn survey population.

I Tierney, D Axworthy, L Smith, S G Ratcliffe.   

Abstract

Thirty-six infants were identified by cytogenetic screening at birth as having balanced rearrangements of their autosomes, and 30 of them took part in a longitudinal study of their development, together with four of their affected sibs. With the exception of one child with a de novo reciprocal translocation who died, all children attended normal schools. Congenital malformations and short stature were present in only one child who had a de novo reciprocal translocation. The IQ scores of the 10 children with de novo translocations were significantly lower than those of the 20 children with familial translocations, but there were children in the de novo group of above average intelligence. Children with familial reciprocal translocations had significantly higher IQ scores than both the Robertsonian translocations and the controls, but the numbers in each category were small and a variety of different chromosomes were involved.

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Mesh:

Year:  1984        PMID: 6694184      PMCID: PMC1049205          DOI: 10.1136/jmg.21.1.45

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


  20 in total

1.  Possible excess of mental handicap and congenital malformations in autosomal reciprocal translocations.

Authors:  J P Fryns; H van den Berghe
Journal:  Ann Genet       Date:  1979

2.  Chromosome aberrations in 2159 consecutive newborn babies.

Authors:  F Sergovich; G H Valentine; A T Chen; R A Kinch; M S Smout
Journal:  N Engl J Med       Date:  1969-04-17       Impact factor: 91.245

3.  Identification of translocation chromosomes by quinacrine fluorescence.

Authors:  W R Breg; D A Miller; P W Allderdice; O J Miller
Journal:  Am J Dis Child       Date:  1972-06

4.  A cytogenetic survey of 11,680 newborn infants.

Authors:  P A Jacobs; M Melville; S Ratcliffe; A J Keay; J Syme
Journal:  Ann Hum Genet       Date:  1974-05       Impact factor: 1.670

5.  Correlation between euploid structural chromosome rearrangements and mental subnormality in humans.

Authors:  P A Jacobs
Journal:  Nature       Date:  1974-05-10       Impact factor: 49.962

6.  Chromosome studies in 5,049 consecutive newborn children.

Authors:  U Friedrich; J Nielsen
Journal:  Clin Genet       Date:  1973       Impact factor: 4.438

7.  Population cytogenetic investigation of newborns in Moscow.

Authors:  N P Bochkov; N P Kuleshov; A N Chebotarev; V I Alekhin; S A Midian
Journal:  Humangenetik       Date:  1974-05-17

8.  Incidence of chromosome aberrations among 11148 newborn children.

Authors:  J Nielsen; I Sillesen
Journal:  Humangenetik       Date:  1975-10-20

9.  A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities.

Authors:  J L Hamerton; N Canning; M Ray; S Smith
Journal:  Clin Genet       Date:  1975-10       Impact factor: 4.438

10.  Chromosome analysis on 930 consecutive newborn children using quinacrine fluorescent banding technique.

Authors:  C C Lin; M M Gedeon; P Griffith; W K Smink; D R Newton; L Wilkie; L M Sewell
Journal:  Hum Genet       Date:  1976-03-12       Impact factor: 4.132

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  6 in total

1.  De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints.

Authors:  D Warburton
Journal:  Am J Hum Genet       Date:  1991-11       Impact factor: 11.025

2.  A non-centromeric C band variant on chromosome 11q23.2.

Authors:  D K Spak; K Johnston; T A Donlon
Journal:  J Med Genet       Date:  1989-08       Impact factor: 6.318

3.  Excess of mental retardation and/or congenital malformation in reciprocal translocations in man.

Authors:  P Steinbach
Journal:  Hum Genet       Date:  1986-08       Impact factor: 4.132

4.  Outcome of de novo balanced translocations ascertained prenatally.

Authors:  D J MacGregor; S Imrie; J L Tolmie
Journal:  J Med Genet       Date:  1989-09       Impact factor: 6.318

5.  SNTG1, the gene encoding gamma1-syntrophin: a candidate gene for idiopathic scoliosis.

Authors:  Stavros Bashiardes; Rose Veile; Missy Allen; Carol A Wise; Mathew Dobbs; Jose A Morcuende; Lazlos Szappanos; John A Herring; Anne M Bowcock; Michael Lovett
Journal:  Hum Genet       Date:  2004-04-16       Impact factor: 4.132

6.  Familial pericentric inversion inv(8)(p23q11).

Authors:  H Boyd; J Kaste; E Hovi; U M Ritanen-Mohammed; H Kääriäinen; A de la Chapelle; A E Lehesjoki
Journal:  J Med Genet       Date:  1994-03       Impact factor: 6.318

  6 in total

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