Literature DB >> 6977293

Interstitial 16q deletion with typical dysmorphic syndrome.

J P Fryns, W Proesmans, G Van Hoey, H Van den Berghe.   

Abstract

Mesh：

Year:  1981        PMID： 6977293

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


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  5 in total

1.  Interstitial deletion and ring chromosome derived from 16q.

Authors:  C M Krauss; D Caldwell; L Atkins
Journal:  J Med Genet       Date:  1987-05       Impact factor: 6.318

2.  Interstitial deletion for a region in the long arm of chromosome 16.

Authors:  C C Lin; R B Lowry; F F Snyder
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

3.  Identical twins with deletion 16q syndrome: evidence that 16q12.2-q13 is the critical band region.

Authors:  F F Elder; J W Ferguson; L H Lockhart
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

4.  Confirmation of a suspected 16q deletion in a dysmorphic child by flow karyotype analysis.

Authors:  A Cooke; J Tolmie; W Darlington; E Boyd; R Thomson; M A Ferguson-Smith
Journal:  J Med Genet       Date:  1987-02       Impact factor: 6.318

5.  Identification and characterization of novel ACD variants: modulation of TPP1 protein level offsets the impact of germline loss-of-function variants on telomere length.

Authors:  Gabrielle Henslee; Christopher L Williams; Pengfei Liu; Alison A Bertuch
Journal:  Cold Spring Harb Mol Case Stud       Date:  2021-02-19
  5 in total

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