Literature DB >> 5173207

Demonstration of the lyon hypothesis in X-linked dominant hypoplastic amelogenesis imperfecta.

M D Berkman, A Singer.   

Abstract

The present study is in agreement with the Lyon hypothesis as indicated by the random pattern of vertical bands of normal-appearing and hypoplastic enamel in the proposita and the mother. Further studies which would quantitate the amount of normal-appearing and hypoplastic enamel in a lage number of teeth with the X-linked hypoplastic type of amelogenesis imperfecta may provide further data in support of the Lyon hypothesis as it applies to this condition. Even though the methodology employed in this study involves nothing more sophisticated than pedigree analysis and clinical appraisal, it purports to demonstrate and support the validity of the Lyon hypothesis concerning amelogenesis imperfecta in man.

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Mesh:

Year:  1971        PMID: 5173207

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN: 0547-6844


  6 in total

1.  X-linked hypophosphatemia: the mutant gene is expressed in teeth as well as in kidney.

Authors:  E D Shields; C R Scriver; T Reade; T M Fujiwara; K Morgan; A Ciampi; S Schwartz
Journal:  Am J Hum Genet       Date:  1990-03       Impact factor: 11.025

2.  Target gene analyses of 39 amelogenesis imperfecta kindreds.

Authors:  Hui-Chen Chan; Ninna M R P Estrella; Rachel N Milkovich; Jung-Wook Kim; James P Simmer; Jan C-C Hu
Journal:  Eur J Oral Sci       Date:  2011-12       Impact factor: 2.612

3.  Mapping of the gene for X-linked amelogenesis imperfecta by linkage analysis.

Authors:  M Lagerström; N Dahl; L Iselius; B Bäckman; U Pettersson
Journal:  Am J Hum Genet       Date:  1990-01       Impact factor: 11.025

Review 4.  Dental enamel development: proteinases and their enamel matrix substrates.

Authors:  John D Bartlett
Journal:  ISRN Dent       Date:  2013-09-16

Review 5.  Amelogenesis Imperfecta; Genes, Proteins, and Pathways.

Authors:  Claire E L Smith; James A Poulter; Agne Antanaviciute; Jennifer Kirkham; Steven J Brookes; Chris F Inglehearn; Alan J Mighell
Journal:  Front Physiol       Date:  2017-06-26       Impact factor: 4.566

6.  Amelogenesis imperfecta in two families with defined AMELX deletions in ARHGAP6.

Authors:  Jan C-C Hu; Hui-Chen Chan; Stephen G Simmer; Figen Seymen; Amelia S Richardson; Yuanyuan Hu; Rachel N Milkovich; Ninna M R P Estrella; Mine Yildirim; Merve Bayram; Chiung-Fen Chen; James P Simmer
Journal:  PLoS One       Date:  2012-12-14       Impact factor: 3.240

  6 in total

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