Literature DB >> 3656373

A chromosome supplement to the London Dysmorphology Database.

J Brandl1, T Grimm.   

Abstract

A supplement to the computerised database for the diagnosis of rare dysmorphic syndromes described by Winter et al is presented, which includes a list of syndromes occurring in patients with unbalanced chromosome aberrations. The extension of the original programme is based on Schinzel's Catalogue of unbalanced chromosome aberrations in man.

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Year:  1987        PMID： 3656373      PMCID： PMC1050208          DOI： 10.1136/jmg.24.8.497

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


  1 in total

1.  A computerised data base for the diagnosis of rare dysmorphic syndromes.

Authors:  R M Winter; M Baraitser; J M Douglas
Journal:  J Med Genet       Date:  1984-04       Impact factor: 6.318
  1 in total
  4 in total

1.  The London Dysmorphology Database.

Authors:  R M Winter; M Baraitser
Journal:  J Med Genet       Date:  1987-08       Impact factor: 6.318

2.  Presentation of an Infant with Chromosome 18p Deletion Syndrome and Asymmetric Septal Hypertrophy.

Authors:  Ayca Kocaaga; Sevgi Yimenicioglu
Journal:  Glob Med Genet       Date:  2022-02-25

3.  The genotype and phenotype of chromosome 18p deletion syndrome: Case series.

Authors:  Qiujie Jin; Rong Qiang; Bo Cai; Xiaobin Wang; Na Cai; Shuai Zhen; Wen Zhai
Journal:  Medicine (Baltimore)       Date:  2021-05-07       Impact factor: 1.889

4.  MarkerDB: an online database of molecular biomarkers.

Authors:  David S Wishart; Brendan Bartok; Eponine Oler; Kevin Y H Liang; Zachary Budinski; Mark Berjanskii; AnChi Guo; Xuan Cao; Michael Wilson
Journal:  Nucleic Acids Res       Date:  2021-01-08       Impact factor: 16.971
  4 in total

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