Literature DB >> 469902

Additional pedigree supporting the frequent origin of XXYY from consecutive meiotic non-disjunction in paternal gametogenesis.

A Rinaldi, N Archidiacono, M Rocchi, G Filippi.   

Abstract

A 48,XXYY Sardinian patient, born to a 46,XX mother heterozygous for the Gd Mediterranean mutant, and to a 46,XY father hemizygous for the same mutant, was found to have a mosaic distribution of G6PD(+) and G6PD(-) peripheral red blood cells. The most likely interpretation of this finding is that the propositus is an additional example of an XXYY zygote derived from a consecutive meiotic non-disjunction during paternal gametogenesis.

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Year:  1979        PMID: 469902      PMCID: PMC1012697          DOI: 10.1136/jmg.16.3.225

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


  4 in total

1.  SUCCESSIVE NON-DISJUNCTION AT FIRST AND SECOND MEIOTIC DIVISION OF SPERMATOGENESIS: EVIDENCE OF CHROMOSOMES AND XG.

Authors:  A DELACHAPELLE; H HORTLING; R SANGER; R R RACE
Journal:  Cytogenetics       Date:  1964

2.  Variability of red cell phenotypes between and within individuals in an unbiased sample of 77 heterozygotes for G6PD deficiency in Sardinia.

Authors:  A Rinaldi; G Filippi; M Siniscalco
Journal:  Am J Hum Genet       Date:  1976-09       Impact factor: 11.025

3.  Xg groups and sex chromosome abnormalities in people of northern European ancestry: an addendum.

Authors:  R Sanger; P Tippett; J Gavin; P Teesdale; G L Daniels
Journal:  J Med Genet       Date:  1977-06       Impact factor: 6.318

4.  Failure to detect linkage between Xg and other X-borne loci in Sardinians.

Authors:  M Siniscalco; G Filippi; B Latte; S Piomelli; M Rattazzi; J Gavin; R Sanger; R R Race
Journal:  Ann Hum Genet       Date:  1966-03       Impact factor: 1.670

  4 in total
  5 in total

Review 1.  48,XXYY, 48,XXXY and 49,XXXXY syndromes: not just variants of Klinefelter syndrome.

Authors:  Nicole Tartaglia; Natalie Ayari; Susan Howell; Cheryl D'Epagnier; Philip Zeitler
Journal:  Acta Paediatr       Date:  2011-04-08       Impact factor: 2.299

2.  Parental origin of the extra chromosomes in polysomy X.

Authors:  C A Leal; J W Belmont; R Nachtman; J M Cantu; C Medina
Journal:  Hum Genet       Date:  1994-10       Impact factor: 4.132

3.  A new look at XXYY syndrome: medical and psychological features.

Authors:  Nicole Tartaglia; Shanlee Davis; Alison Hench; Sheela Nimishakavi; Renee Beauregard; Ann Reynolds; Laura Fenton; Lindsey Albrecht; Judith Ross; Jeannie Visootsak; Robin Hansen; Randi Hagerman
Journal:  Am J Med Genet A       Date:  2008-06-15       Impact factor: 2.802

4.  Molecular diagnostic testing for Klinefelter syndrome and other male sex chromosome aneuploidies.

Authors:  Karl Hager; Kori Jennings; Seiyu Hosono; Susan Howell; Jeffrey R Gruen; Scott A Rivkees; Nicole R Tartaglia; Henry M Rinder
Journal:  Int J Pediatr Endocrinol       Date:  2012-04-23

5.  Brain and behavior in 48, XXYY syndrome.

Authors:  Alli P Hanley; Jonathan D Blumenthal; Nancy Raitano Lee; Eva H Baker; Liv S Clasen; Jay N Giedd
Journal:  Neuroimage Clin       Date:  2015-04-15       Impact factor: 4.881

  5 in total

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