TITLE

Pathology/cytology

PUB. DATE
August 1997
SOURCE
Clinical & Investigative Medicine;Aug97 Supplement, Vol. 20, pS70
SOURCE TYPE
Academic Journal
DOC. TYPE
Abstract
ABSTRACT
Presents an abstract of the research manuscript `What is the importance of atypical glandular cells of undetermined significance in dysplasia clinic patients?,' by J.L. Parai et al.
ACCESSION #
9708236838

 

Related Articles

  • Longevity in Schimke Immuno-osseous dysplasia. Lou, S.; Lamfers, P.; McGuire, N.; Boerkoel, C.F. // Journal of Medical Genetics;Dec2002, Vol. 39 Issue 12, p922 

    Studies longevity in Schimke immuno-osseous dysplasia. Genetic mutations; Disease severity; Clinical symptoms.

  • Fatal outcome in a female monozygotic twin with X-linked hypohydrotic ectodermal dysplasia (XLHED) due to a de novo t(X;9) translocation with probable disruption of the EDA gene. Zankl, Andreas; Addor, Marie-Claude; Cousin, Pascal; Gaide, Anne-Claude; Gudinchet, Francois; Schorderet, Daniel F.; Zankl, A; Addor, M C; Cousin, P; Gaide, A C; Gudinchet, F; Schorderet, D F // European Journal of Pediatrics;2001, Vol. 160 Issue 5, p296 

    Unlabelled: Ectodermal dysplasias are a group of congenital disorders with defective development of the epidermis and its appendages. X-linked hypohydrotic ectodermal dysplasia (XLHED; OMIM 305100) is the most common form of ectodermal dysplasia. We report on two monozygotic twin...

  • Response to the Letter by Professor Grosshans. Detlev K√∂hler, Lars; M√∂hrenschlager, Matthias; Ring, Johannes // Acta Dermato-Venereologica;10/28/98, Vol. 78 Issue 6, p481 

    Presents a reply to the lecture of Professor Grosshans on the nature of congenital leukonychia totalis. Symptoms of ectodermal dysplasia; Evidences of leukonychia totalis; Analysis of the genetic background of the disease.

  • Analysis of the p63 gene in classical EEC syndrome, related syndromes, and non-syndromic orofacial clefts. Barrow, L.L.; van Bokhoven, H.; Daack-Hirsch, S.; Andersen, T.; van Beersum, S.E.C.; Gorlin, R.; Murray, J.C. // Journal of Medical Genetics;Aug2002, Vol. 39 Issue 8, p559 

    Analyzes the p63 gene in classical ectrodactyly ectodermal dysplasia-related syndromes, related syndromes and non-syndromic orofacial clefts. Key issues of interest; Analysis of pertinent topics and relevant issues; Theoretical significance to medical genetics.

  • The phenotype of survivors of campomelic dysplasia. Mansour, S.; Offiah, A.C.; McDowall, S.; Sim, P.; Tolmie, J.; Hall, C. // Journal of Medical Genetics;Aug2002, Vol. 39 Issue 8, p597 

    Studies the phenotype of survivors of campomelic dysplasia. Key issues of interest; Analysis of pertinent topics and relevant issues; Theoretical significance to medical genetics.

  • Christ-Siemens-Touraine syndrome.  // Taber's Cyclopedic Medical Dictionary (2009);2009, Issue 21, p445 

    A definition of the term "Christ-Siemens-Touraine syndrome" which refers to a rare congenital disease marked by hairlessness and inability to sweat, among others, is presented.

  • Alagille syndrome.  // Taber's Cyclopedic Medical Dictionary (2009);2009, Issue 21, p70 

    A definition of the term "Alagille syndrome," which refers to a rare congenital syndrome in which arteriohepatic dysplasia is associated with developmental anomalies of the face, heart, kidneys, muscle and nervous system, is presented.

  • Clinical and radiographic features of multiple epiphyseal dysplasia not linked to the COMP or type IX collagen genes. Mortier, Geert R; Chapman, Kathryn; Leroy, Jules L; Briggs, Michael D // European Journal of Human Genetics;Aug2001, Vol. 9 Issue 8, p606 

    Multiple epiphyseal dysplasia (MED) is a mild chondrodysplasia affecting the structural integrity of cartilage and causing early-onset osteoarthrosis in adulthood. The condition is genetically heterogeneous. Mutations in the COMP gene and in two genes (COL9A2; COL9A3), coding respectively for...

  • Camurati-Engelmann Disease. Vanhoenacker, F. M.; Janssens, K.; Van Hul, W.; Gershoni-Baruch, R.; Brik, R.; De Schepper, A. M. // Acta Radiologica;Jul2003, Vol. 44 Issue 4, p430 

    Abstract Purpose: To present a retrospective overview of the clinical and radiological features of Camurati-Engelmann disease (CED) in a large family with genetically proven CED. Material and Methods: Clinical features and imaging studies were available in 8 affected patients out of a large...

Share

Read the Article

Courtesy of THE LIBRARY OF VIRGINIA

Sorry, but this item is not currently available from your library.

Try another library?
Sign out of this library

Other Topics