Literature DB >> 890095

Ring 13 chromosome associated with microcephaly, congenital heart defect, intrauterine growth retardation, and abnormal skin pigmentation.

R B Lowry, F J Dill.   

Abstract

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Mesh：

Year:  1977        PMID： 890095

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN： 0547-6844


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  2 in total

1.  Study of two cases of ring 13 chromosome using high-resolution banding.

Authors:  I M Jones; C G Palmer; D D Weaver; M E Hodes
Journal:  Am J Hum Genet       Date:  1981-03       Impact factor: 11.025

Review 2.  Ring chromosome 13: lack of distinct syndromes based on different breakpoints on 13q.

Authors:  C A Brandt; J M Hertz; M B Petersen; F Vogel; H Noer; M Mikkelsen
Journal:  J Med Genet       Date:  1992-10       Impact factor: 6.318
  2 in total

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