Literature DB >> 4691556

A problem in diagnosis of primary versus secondary microcephaly.

Q H Qazi, T E Reed.   

Abstract

Mesh:

Year:  1973        PMID: 4691556     DOI: 10.1111/j.1399-0004.1973.tb01121.x

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


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  6 in total

1.  Primary autosomal recessive microcephaly (MCPH1) maps to chromosome 8p22-pter.

Authors:  A P Jackson; D P McHale; D A Campbell; H Jafri; Y Rashid; J Mannan; G Karbani; P Corry; M I Levene; R F Mueller; A F Markham; N J Lench; C G Woods
Journal:  Am J Hum Genet       Date:  1998-08       Impact factor: 11.025

Review 2.  Autosomal recessive primary microcephaly (MCPH): a review of clinical, molecular, and evolutionary findings.

Authors:  C Geoffrey Woods; Jacquelyn Bond; Wolfgang Enard
Journal:  Am J Hum Genet       Date:  2005-03-31       Impact factor: 11.025

3.  A biometric analysis of brain size in micrencephalics.

Authors:  M A Hofman
Journal:  J Neurol       Date:  1984       Impact factor: 4.849

4.  Practice parameter: Evaluation of the child with microcephaly (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society.

Authors:  Stephen Ashwal; David Michelson; Lauren Plawner; William B Dobyns
Journal:  Neurology       Date:  2009-09-15       Impact factor: 9.910

Review 5.  MCPH1: a window into brain development and evolution.

Authors:  Jeremy N Pulvers; Nathalie Journiac; Yoko Arai; Jeannette Nardelli
Journal:  Front Cell Neurosci       Date:  2015-03-27       Impact factor: 5.505

6.  Abnormal cranium development in children and adolescents affected by syndromes or diseases associated with neurodysfunction.

Authors:  Agnieszka Guzik; Lidia Perenc; Mariusz Drużbicki; Justyna Podgórska-Bednarz
Journal:  Sci Rep       Date:  2021-02-03       Impact factor: 4.379

  6 in total

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