Literature DB >> 4064371

Centromere heteromorphism in chromosome 19.

U Friedrich.   

Abstract

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Year:  1985        PMID： 4064371     DOI： 10.1111/j.1399-0004.1985.tb00412.x

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


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  3 in total

1.  Simultaneous de novo interstitial deletion of 16q21 and intercalary duplication of 19q in a retarded infant with minor dysmorphic features.

Authors:  U Trautmann; R A Pfeiffer; U Seufert-Satomi; H U Tietze
Journal:  J Med Genet       Date:  1993-04       Impact factor: 6.318

2.  Three-point linkage analysis employing C3 and 19cen markers assigns the myotonic dystrophy gene to 19q.

Authors:  U Friedrich; H Brunner; D Smeets; E Lambermon; H H Ropers
Journal:  Hum Genet       Date:  1987-03       Impact factor: 4.132

3.  C-banding and AgNOR-staining were still effective complementary methods to indentify chromosomal heteromorphisms and some structural abnormalities in prenatal diagnosis.

Authors:  Jian Jiang Zhu; Hong Qi; Li Rong Cai; Xiao Hui Wen; Wen Zeng; Guo Dong Tang; Yao Luo; Ran Meng; Xue Qun Mao; Shao Qin Zhang
Journal:  Mol Cytogenet       Date:  2019-09-18       Impact factor: 2.009
  3 in total

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