Literature DB >> 10330367

Rett syndrome in a boy with a 47,XXY karyotype.

J Salomão Schwartzman, M Zatz, L dos Reis Vasquez, R Ribeiro Gomes, C P Koiffmann, C Fridman, P Guimarães Otto.   

Abstract

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Year:  1999        PMID： 10330367      PMCID： PMC1377923          DOI： 10.1086/302424

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  4 in total

1.  MECP2 mutation in non-fatal, non-progressive encephalopathy in a male.

Authors:  B Imessaoudene; J P Bonnefont; G Royer; V Cormier-Daire; S Lyonnet; G Lyon; A Munnich; J Amiel
Journal:  J Med Genet       Date:  2001-03       Impact factor: 6.318

Review 2.  Brief report: systematic review of Rett syndrome in males.

Authors:  Brian Reichow; Annie George-Puskar; Tara Lutz; Isaac C Smith; Fred R Volkmar
Journal:  J Autism Dev Disord       Date:  2015-10

Review 3.  Rett Syndrome: Reaching for Clinical Trials.

Authors:  Lucas Pozzo-Miller; Sandipan Pati; Alan K Percy
Journal:  Neurotherapeutics       Date:  2015-07       Impact factor: 7.620

Review 4.  MECP2 disorders: from the clinic to mice and back.

Authors:  Laura Marie Lombardi; Steven Andrew Baker; Huda Yahya Zoghbi
Journal:  J Clin Invest       Date:  2015-08-03       Impact factor: 14.808
  4 in total

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