Newborn Care - New Treatments, May 2, 2008

Click here to view next page of this article / Newborn Care and Newborn Infant / Fetal Assessment ... Previous offspring with chromosome abnormality, especially trisomy Chromosome abnormality in either parent, especially translocation Need to...
http://www.ccspublishing.com/journals2a/newborn_care.htm

 

Incontinentia pigmenti.DermNet NZ

DermNet NZ / Ad ... What causes incontinentia pigmenti? Incontinentia pigmenti is a dominant X-linked disease. ... Dominant X-linked disease means that a female with only one copy of the abnormal gene...
http://www.dermnetnz.org/systemic/incontinentia-pigmenti.html

 

eMedicine - Anemia, Sickle Cell : Article by Ali TahereMedicine - Anemia, Sickle Cell : Article by

Home / Specialties / Reference Centers / All Sources eMedicine Medscape Drug Reference MEDLINE / Anemia Resource Center / Anemia Resource Center / View all Anemia Articles / Anemia Multimedia Library / Quick Find / Authors & Editors /...
http://www.emedicine.com/emerg/topic26.htm

 

Wellcome Trust Sanger Institute Press Releases

Username: Password: / Information / Introduction / Press Releases / Institute Overview / Seminars / Travel Directions / Publications / Press Releases 2008 ... "From our study of one gene involved in an X-linked disease,...
http://www.sanger.ac.uk/Info/Press/2005/050316.shtml

 

Familial Nephritis and Alport Syndrome - New Treatments, May 2, 2008

Click here to view next page of this article / Familial Nephritis/Alport Syndrome / Introduction ... Most affected boys develop deafness by adolescence, and females who have X-linked disease may suffer hearing impairment in...
http://www.medical-library.org/journals3a/alport_syndrome.htm

 

Primary Immunodeficiency Service - TeamHartley

Primary Immunodeficiency Service / Great Ormond Street Hospital for Children NHS Trust / Parent / Patient /GP Information sheet / X-linked Lymphoproliferative Disease / (Duncan’s syndrome) / How Common is XLP ... This is an...
http://www.teamhartley.co.uk/whatis.asp

 

Research Licences for Guy's Hospital, London

... (PGD has been applied in a number of centres around the world for a variety of indications, including the analysis of numerical and structural chromosomal abnormalities, identification of sex for X-linked disease and...
http://www.hfea.gov.uk/cps/rde/xchg/SID-3F57D79B-B06AEE07/hfea/hs.xsl/1084.html

 

Altered Cochlear Fibrocytes in a Mouse Model of DFN3 Nonsyndromic Deafness -- Minowa et al. 285 (5432): 1408 -- Science

Jump to: Page Content, Section Navigation, Site Navigation, Site Search, Account Information, or Site Tools. Note to users. ... A Phenotype Map of the Mouse X Chromosome: Models for Human X-linked Disease. ...
http://www.sciencemag.org/cgi/content/short/285/5432/1408

 

Orphanet Journal of Rare Diseases |Full text |Lowe syndrome

Skip to main content / 17-Dec-2007  / Home | / Browse articles | / Search | / Weblinks | / Submit article | ... It is a uncommon, panethnic, X-linked disease, with estimated prevalence in the general population of...
http://www.ojrd.com/content/1/1/16

 

Genetic diagnosis before implantation -- Delhanty et al. 315 (7112): 828 -- BMJ

... Sexing the embryo to avoid X linked disease remains the commonest reason for preimplantation diagnosis, now optimally carried out by the molecular cytogenetic technique of FISH (fluorescent in situ hybridisation) with DNA...
http://www.bmj.com/cgi/content/full/315/7112/828

 
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