Literature DB >> 5313150

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

S Gilgenkrantz, J P Grilliat, D A Vautrin, B Plouvier, C Cabrol.   

Abstract

Mesh：

Year:  1970        PMID： 5313150

Source DB:  PubMed          Journal:  Ann Genet        ISSN： 0003-3995


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  4 in total

1.  Klinefelter's syndrome associated with a D/D translocation.

Authors:  M Sparagana; G P Smith
Journal:  J Med Genet       Date:  1975-09       Impact factor: 6.318

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

Authors:  U Hillig; J J Hoo
Journal:  Humangenetik       Date:  1974

3.  Patterns of D chromosome involvement in human (DqDq) and (DqGq) Robertsonian rearrangements.

Authors:  F Hecht; W J Kimberling
Journal:  Am J Hum Genet       Date:  1971-07       Impact factor: 11.025

4.  On the non-random involvement of D-group chromosomes in centric fusion translocations in man.

Authors:  M Nagel; H Hoehn
Journal:  Humangenetik       Date:  1971
  4 in total

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