Literature DB >> 5295698

[Familial Cc-F translocation determining a trisomy for the short arm of chromosome 12].

J Lejeuen, R Berger, M O Réthoré, C Salmon, M Kaplan.   

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Year:  1966        PMID： 5295698

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


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  9 in total

1.  Trisomy 9p resulting from maternal 9/21 translocation.

Authors:  I Sŭbrt; B Blehová; B Pallová
Journal:  Hum Genet       Date:  1976-05-19       Impact factor: 4.132

2.  47,+(9q-) in unrelated three children with plasma growth hormone deficiency.

Authors:  H Fujita; M Shimazaki; T Takeuchi; Y Hayakawa; T Oura
Journal:  Hum Genet       Date:  1976-03-12       Impact factor: 4.132

Review 3.  Genetics of the +p9 syndrome.

Authors:  I W Lurie; G I Lazjuk; D B Gurevich; S S Usoev
Journal:  Hum Genet       Date:  1976-04-15       Impact factor: 4.132

4.  [Giemsa-R-banding analysis of the trisomy 9p and report of a new case].

Authors:  M O Rethoré; H Hoehn; H D Rott; J Couturier; B Dutrillaux; J Lejeune
Journal:  Humangenetik       Date:  1973-04-16

5.  Identification of a familial 19-21 translocation by Q and G band patterns.

Authors:  W Vogel; B Löning
Journal:  Humangenetik       Date:  1973-05-25

6.  On the localization of genes on certain autosomes of man through chromosome aberrations. 3. Exclusion of the possibility of gene assignment.

Authors:  K Bender; K Burckhardt
Journal:  Humangenetik       Date:  1970

7.  Presumed trisomy for the short arm of chromosome No. 9 not due to inherited translocation.

Authors:  H Hoehn; W Engel; H Reinwein
Journal:  Humangenetik       Date:  1971

8.  Trisomy 12p due to familial t(12p-,6q plus) translocation.

Authors:  J P Fryns; H Van Den Berghe
Journal:  Humangenetik       Date:  1974

9.  Trisomy 9p resulting from de novo 9/15 translocation and a 9p isochromosome.

Authors:  K R Sandig; J Mücke; H Veit
Journal:  Hum Genet       Date:  1979-11       Impact factor: 4.132
  9 in total

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