Literature DB >> 5706055

Two patients with a 46,XX,Er chromosome constitution.

J Leisti, U Gripenberg, E Kivalo, J Palo, B von Schoulz, E Suomalainen.   

Abstract

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Year:  1968        PMID： 5706055     DOI： 10.1111/j.1651-2227.1968.tb07318.x

Source DB:  PubMed          Journal:  Acta Paediatr Scand        ISSN： 0001-656X


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  7 in total

1.  The r(20) syndrome.

Authors:  R Herva; I Saarinen; L Leikkonen
Journal:  J Med Genet       Date:  1977-08       Impact factor: 6.318

Review 2.  [Ring chromosome 18. 18p-/18q- -deletion-syndrome].

Authors:  J Kunze; E Stephan; M Tolksdorf
Journal:  Humangenetik       Date:  1972

Review 3.  Partial monosomies 18. Review of cytogenetical and phenotypical variants.

Authors:  I W Lurie; G I Lazjuk
Journal:  Humangenetik       Date:  1972

Review 4.  Malformations of kidney and urinary tract in common chromosomal aberrations. II. Morphogenetic studies.

Authors:  G Töndury
Journal:  Humangenetik       Date:  1973-03-23

5.  Extensive cytological damage caused by measles in African children.

Authors:  U Gripenberg; C Forbes
Journal:  J Med Genet       Date:  1974-06       Impact factor: 6.318

6.  Ring chromosome 18 (46, XX, 18r).

Authors:  A Cenani; R A Pfeiffer; H A Simon
Journal:  Humangenetik       Date:  1969

7.  Median facial cleft associated with ring E chromosome.

Authors:  K W Dumars; L G Carnahan; R V Barrett
Journal:  J Med Genet       Date:  1970-03       Impact factor: 6.318
  7 in total

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