Literature DB >> 3757307

Segregation analysis of balanced pericentric inversions in pedigree data.

S L Sherman, L Iselius, P Gallano, K Buckton, S Collyer, R DeMey, U Kristoffersson, J Lindsten, M Mikkelsen, N E Morton.   

Abstract

The results of the recent European collaborative prenatal study suggested a segregation distortion of balanced pericentric inversions from carrier fathers but not carrier mothers (Boué & Gallano 1984). In an attempt to confirm these unexpected results, we examined 216 pedigrees with balanced pericentric inversions collected from three centers and from the literature. We were unable to detect any significant deviation from the expected 1:1 segregation of balanced pericentric inversions to normal karyotypes among the offspring of either carrier parent. To clarify the discrepancy between the studies, we reanalyzed the data from the prenatal study using all karyotyped individuals and, assuming conventional ascertainment rules, found a normal segregation pattern. We conclude that balanced pericentric inversions segregate normally in both males and females and that some retrospectively selected pedigrees were included as prospective in the prenatal study and this misclassification caused the apparent segregation distortion from carrier fathers.

Mesh:

Year:  1986        PMID: 3757307     DOI: 10.1111/j.1399-0004.1986.tb00575.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  12 in total

1.  A malformed child with a recombinant chromosome 7, rec(7) dup p, derived from a maternal pericentric inversion inv(7)(p15q36).

Authors:  A Delicado; E Escribano; I Lopez Pajares; A Diaz de Bustamante; S Carrasco
Journal:  J Med Genet       Date:  1991-02       Impact factor: 6.318

Review 2.  Sperm chromosome analysis of a man heterozygous for a pericentric inversion of chromosome 20.

Authors:  J Jenderny; J Gebauer; G Röhrborn; A Rüger
Journal:  Hum Genet       Date:  1992-04       Impact factor: 4.132

3.  Investigation of the origins of human autosomal inversions.

Authors:  N Simon Thomas; Victoria Bryant; Vivienne Maloney; Annette E Cockwell; Patricia A Jacobs
Journal:  Hum Genet       Date:  2008-05-10       Impact factor: 4.132

4.  De novo inv(17)(p11.2q21.3) in an intellectually disabled girl: appraisal of 21 inv(17) constitutional instances.

Authors:  Miriam Partida-Pérez; María G Domínguez; Vivian Alejandra Neira; Luis E Figuera; Horacio Rivera
Journal:  J Genet       Date:  2012-08       Impact factor: 1.166

5.  Breakpoint cloning and haplotype analysis indicate a single origin of the common Inv(10)(p11.2q21.2) mutation among northern Europeans.

Authors:  Mette Gilling; Jörn S Dullinger; Stefan Gesk; Simone Metzke-Heidemann; Reiner Siebert; Thomas Meyer; Karen Brondum-Nielsen; Niels Tommerup; Hans-Hilger Ropers; Zeynep Tümer; Vera M Kalscheuer; N Simon Thomas
Journal:  Am J Hum Genet       Date:  2006-03-17       Impact factor: 11.025

6.  Genetic risk for recombinant 8 syndrome and the transmission rate of balanced inversion 8 in the Hispanic population of the southwestern United States.

Authors:  A C Smith; K Spuhler; T M Williams; T McConnell; E Sujansky; A Robinson
Journal:  Am J Hum Genet       Date:  1987-12       Impact factor: 11.025

7.  Segregation analysis in a man heterozygous for a pericentric inversion of chromosome 7 (p13;q36) by sperm chromosome studies.

Authors:  J Navarro; J Benet; M R Martorell; C Templado; J Egozcue
Journal:  Am J Hum Genet       Date:  1993-07       Impact factor: 11.025

8.  Cytogenetic analysis of sperm from a man heterozygous for a pericentric inversion, inv (3) (p25q21).

Authors:  R H Martin
Journal:  Am J Hum Genet       Date:  1991-05       Impact factor: 11.025

9.  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

10.  Pericentric inversions in man: personal experience and review of the literature.

Authors:  A Kleczkowska; J P Fryns; H Van den Berghe
Journal:  Hum Genet       Date:  1987-04       Impact factor: 4.132

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