Literature DB >> 4442889

A case of 48,XXYY--paternal origin of the extra X chromosome.

U Hillig, J J Hoo.   

Abstract

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Year:  1974        PMID： 4442889     DOI： 10.1007/BF00283317

Source DB:  PubMed          Journal:  Humangenetik        ISSN： 0018-7348


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  6 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.  Combined Klinefelter-Down syndrome or XXYY syndrome?

Authors:  H Singer; H Zankl; A Rodewald-Rudescu
Journal:  Humangenetik       Date:  1973-09-20

3.  Bone abnormalities and XXYY.

Authors:  T S Davies
Journal:  Lancet       Date:  1970-01-10       Impact factor: 79.321

4.  [The XXYY variant of Klinefelter's syndrome (author's transl)].

Authors:  O P Hornstein; H D Rott; G Schwanitz; G Grosse
Journal:  Dtsch Med Wochenschr       Date:  1974-02-08       Impact factor: 0.628

5.  [Syndrome 47, XXYY, 13-, 14-, t(13q14q)+].

Authors:  S Gilgenkrantz; J P Grilliat; D A Vautrin; B Plouvier; C Cabrol
Journal:  Ann Genet       Date:  1970-09

6.  The 48, XXYY syndrome.

Authors:  C E Parker; J Mavalwala; J Melnyk; C H Fish
Journal:  Am J Med       Date:  1970-06       Impact factor: 4.965
  6 in total
  1 in total

1.  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
  1 in total

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