Literature DB >> 1605257

Completeness of catalogs of autosomal dominant, autosomal recessive, and X-linked phenotypes.

L P ten Kate1.   

Abstract

The completeness of McKusick's catalogs of Mendelian Inheritance in Man (MIM) as to the number of phenotypes included was studied by estimating the degree of concordance with the Dutch Gene Catalog of the Department of Medical Genetics of the University of Groningen, The Netherlands. On a total of 355 Mendelian phenotypes described in persons living in The Netherlands or originating from this country, there were nine disease entities which were not present in MIM. As judged from this comparison MIM attains 97.5% completeness (95% CI: 95.3-98.7%). Similar comparisons with data from other countries are needed before a final conclusion can be reached. Corresponding contributors in different countries or linguistic areas might further improve MIM's completeness.

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Mesh:

Year:  1992        PMID: 1605257     DOI: 10.1002/ajmg.1320430320

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  18 in total

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Journal:  Basic Res Cardiol       Date:  1975 Jul-Aug       Impact factor: 17.165

2.  Physical fine mapping of genes underlying X-linked deafness and non fra (X)-X-linked mental retardation at Xq21.

Authors:  I Bach; D Robinson; N Thomas; H H Ropers; F P Cremers
Journal:  Hum Genet       Date:  1992-08       Impact factor: 4.132

3.  Is Shwachman syndrome (McKusick 26040) a chromosome breakage syndrome?

Authors:  C P Koiffmann; C H Gonzalez; D H Souza; E G Romani; C A Kim; A Wajntal
Journal:  Hum Genet       Date:  1991-05       Impact factor: 4.132

4.  Webbed fingers.

Authors:  Adrian E Flatt
Journal:  Proc (Bayl Univ Med Cent)       Date:  2005-01

5.  Brief report: response to methylphenidate in two children with Williams syndrome.

Authors:  T J Power; N J Blum; S M Jones; P E Kaplan
Journal:  J Autism Dev Disord       Date:  1997-02

6.  Neurofibromatosis with cardiac involvement.

Authors:  H Noubani; E Poon; R S Cooper; E Kahn; M Kazadevich; V A Parnell
Journal:  Pediatr Cardiol       Date:  1997 Mar-Apr       Impact factor: 1.655

Review 7.  Fishing forward and reverse: Advances in zebrafish phenomics.

Authors:  Ricardo Fuentes; Joaquín Letelier; Benjamin Tajer; Leonardo E Valdivia; Mary C Mullins
Journal:  Mech Dev       Date:  2018-08-18       Impact factor: 1.882

8.  Brittle cornea syndrome: an heritable connective tissue disorder distinct from Ehlers-Danlos syndrome type VI and fragilitas oculi, with spontaneous perforations of the eye, blue sclerae, red hair, and normal collagen lysyl hydroxylation.

Authors:  P M Royce; B Steinmann; A Vogel; U Steinhorst; A Kohlschuetter
Journal:  Eur J Pediatr       Date:  1990-04       Impact factor: 3.183

Review 9.  Syringomyelia: a brief review of ontogenetic, experimental and clinical aspects.

Authors:  E Donauer; K Rascher
Journal:  Neurosurg Rev       Date:  1993       Impact factor: 3.042

10.  Familial Sneddon's syndrome.

Authors:  A Lossos; T Ben-Hur; Z Ben-Nariah; C Enk; M Gomori; D Soffer
Journal:  J Neurol       Date:  1995-02       Impact factor: 4.849

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