Literature DB >> 12476462

45,X/46,XY mosaicism and fragile X syndrome.

Shannon L Banes1, Michael L Begleiter, Merlin G Butler.   

Abstract

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12476462      PMCID: PMC5438263          DOI: 10.1002/ajmg.a.10006

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


× No keyword cloud information.
  8 in total

1.  A case of mosaicism with fragile-X and XXY components.

Authors:  S Deb; V A Cowie; C Timberlake
Journal:  Br J Psychiatry       Date:  1987-05       Impact factor: 9.319

2.  46XY/47XYY mosaicism and fragile X.

Authors:  J Bodurtha; C Jackson-Cook; A Maddalena; J Piserchio; R Waller
Journal:  Clin Genet       Date:  1993-08       Impact factor: 4.438

3.  Asymmetry of methylation with FMR-1 full mutation in two 45,X/46,XX mosaic females associated with normal intellect.

Authors:  L R Shapiro; R J Simensen; P L Wilmot; G S Fisch; B K Vibert; R G Fenwick; J Tarleton; M C Phelan
Journal:  Am J Med Genet       Date:  1994-07-15

Review 4.  Sex chromosomal and autosomal aneuploidy in the fragile X syndrome.

Authors:  A E Chudley
Journal:  Birth Defects Orig Artic Ser       Date:  1990

5.  Origin of the supernumerary X chromosome in a patient with fragile X and Klinefelter syndrome.

Authors:  K G Kupke; A L Soreng; U Müller
Journal:  Am J Med Genet       Date:  1991 Feb-Mar

6.  46,XY/47,XYY male with the fragile X syndrome: cytogenetic and molecular studies.

Authors:  A Milunsky; X Huang; J A Amos; J Herskowitz; L A Farrer; H E Wyandt
Journal:  Am J Med Genet       Date:  1993-03-01

7.  The concurrence of Klinefelter syndrome and fragile X syndrome.

Authors:  J P Fryns; H Van den Berghe
Journal:  Am J Med Genet       Date:  1988 May-Jun

8.  XY/XXY mosaicism and fragile X syndrome.

Authors:  J P Fryns; A Kleczkowska; E Kubień; P Petit; M Haspeslagh; I Lindemans; H Van Den Berghe
Journal:  Ann Genet       Date:  1983
  8 in total
  2 in total

1.  Dual diagnoses in 152 patients with Turner syndrome: Knowledge of the second condition may lead to modification of treatment and/or surveillance.

Authors:  Kelly L Jones; Erin A McNamara; Mauro Longoni; Danny E Miller; Mersedeh Rohanizadegan; Laura A Newman; Frances Hayes; Lynne L Levitsky; Betty L Herrington; Angela E Lin
Journal:  Am J Med Genet A       Date:  2018-08-06       Impact factor: 2.802

2.  Klinefelter syndrome mosaicism in boys with neurodevelopmental disorders: a cohort study and an extension of the hypothesis.

Authors:  Svetlana G Vorsanova; Irina A Demidova; Alexey D Kolotii; Oksana S Kurinnaia; Victor S Kravets; Ilya V Soloviev; Yuri B Yurov; Ivan Y Iourov
Journal:  Mol Cytogenet       Date:  2022-03-05       Impact factor: 2.009

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.