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RAPADILINO Syndrome (5)

See Also:

Sites:

http://hmg.oxfordjournals.org/cgi/content/full/12/21/2837

» Molecular Defect of RAPADILINO Syndrome Expands the Phenotype Spectrum of RECQL Diseases
Paper published in Human Molecular Genetics in 2003.
http://hmg.oxfordjournals.org/cgi/content/full/12/21/2837

» Online Mendelian Inheritance in Man
Lists references, clinical symptoms, and genetics.
http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=266280

http://www.orpha.net/consor/cgi-bin/Disease_Search.php?lng=EN&Lng=EN&Expert=3021&data_id=2716&title=RAPADILINO-syndrome&addSigns=1

» Orphanet: RAPADILINO Syndrome
Portal for information on this rare disorder.
http://www.orpha.net/consor/cgi-bin/Disease_Search.php?lng=EN&Lng=EN&Expert=3021&data_id=2716&title=RAPADILINO-syndrome&addSigns=1

http://www.humpath.com/RAPADILINO-syndrome

» RAPADILINO Syndrome
Provides a description of the symptoms this autosomal recessive disorder characterized by short stature, radial ray defects and other malformations.
http://www.humpath.com/RAPADILINO-syndrome

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Last Updated: 2007-01-02 16:35:21

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