Literature DB >> 7337958

Abnormal phenotype in a child with the same balanced translocation (5;7)(p15;q22) as his father.

M R Caballín, R Miró, J Egozcue.   

Abstract

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Mesh：

Year:  1981        PMID： 7337958     DOI： 10.1111/j.1399-0004.1981.tb01053.x

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


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  3 in total

1.  Absence of linkage of Noonan syndrome to the neurofibromatosis type 1 locus.

Authors:  M Sharland; R Taylor; M A Patton; S Jeffery
Journal:  J Med Genet       Date:  1992-03       Impact factor: 6.318

2.  Franceschetti syndrome in a child with a de novo balanced translocation (5;13)(q11;p11) and significant decrease of hexosaminidase B.

Authors:  P Balestrazzi; M A Baeteman; M G Mattei; J F Mattei
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

3.  Noonan syndrome - a new survey.

Authors:  Alireza Tafazoli; Peyman Eshraghi; Zahra Kamel Koleti; Mohammadreza Abbaszadegan
Journal:  Arch Med Sci       Date:  2016-12-19       Impact factor: 3.318
  3 in total

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