Literature DB >> 7362200

A G-band study of chromosomes in liveborn infants.

K E Buckton, M L O'Riordan, S Ratcliffe, J Slight, M Mitchell, S McBeath, A J Keay, D Barr, M Short.   

Abstract

The results of a chromosome survey of 3993 liveborn infants, the majority of which have been studied using G-banding, are reported. The frequency of all types of chromosome abnormalities detected was similar to that found in previous newborn surveys, which were carried out on different socio-economic structure, but the incidence of aneuploid chromosome abnormalities was comparable in the two localities.

Entities:  

Mesh:

Year:  1980        PMID: 7362200     DOI: 10.1111/j.1469-1809.1980.tb01556.x

Source DB:  PubMed          Journal:  Ann Hum Genet        ISSN: 0003-4800            Impact factor:   1.670


  26 in total

Review 1.  Chromosome imbalance, normal phenotype, and imprinting.

Authors:  L Bortotto; E Piovan; R Furlan; H Rivera; O Zuffardi
Journal:  J Med Genet       Date:  1990-09       Impact factor: 6.318

2.  Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of banding.

Authors:  P A Jacobs; C Browne; N Gregson; C Joyce; H White
Journal:  J Med Genet       Date:  1992-02       Impact factor: 6.318

3.  Replication studies in the 16p+ variant.

Authors:  P W Thompson; S H Roberts; S M Rees
Journal:  Hum Genet       Date:  1990-03       Impact factor: 4.132

4.  Y-SNP haplogroups related to the Yqh+ heteromorphism in the Mexican northwestern population.

Authors:  Enrique Jhonatan Romo-Martínez; Gabriela Martínez-Cortés; Reyna Lucía Barajas-Torres; Rodrigo Rubi-Castellanos; María Teresa Magaña-Torres; Héctor Rangel-Villalobos; Juan Ramón González-García
Journal:  J Genet       Date:  2012       Impact factor: 1.166

5.  Non C-banding variants in some normal families might be homogeneously staining regions.

Authors:  G C Webb; E J Krumins; S Z Eichenbaum; L E Voullaire; E Earle; K H Choó
Journal:  Hum Genet       Date:  1989-04       Impact factor: 4.132

6.  Fathers' occupation and pregnancy outcome.

Authors:  A D McDonald; J C McDonald; B Armstrong; N M Cherry; A D Nolin; D Robert
Journal:  Br J Ind Med       Date:  1989-05

Review 7.  Directly transmitted unbalanced chromosome abnormalities and euchromatic variants.

Authors:  J C K Barber
Journal:  J Med Genet       Date:  2005-08       Impact factor: 6.318

Review 8.  Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysis.

Authors:  M G Mattei; N Souiah; J F Mattei
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

9.  Molecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: clinical implications.

Authors:  J Leana-Cox; L Jenkins; C G Palmer; R Plattner; L Sheppard; W L Flejter; J Zackowski; F Tsien; S Schwartz
Journal:  Am J Hum Genet       Date:  1994-05       Impact factor: 11.025

10.  Hydatidiform mole: parental chromosome aberrations in partial and complete moles.

Authors:  L O Vejerslev; R A Fisher; U Surti; N Wake
Journal:  J Med Genet       Date:  1987-10       Impact factor: 6.318

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