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- Q3297103 subject Q8280463.
- Q3297103 abstract "1p36 deletion syndrome (also known as monosomy 1p36) is a congenital genetic disorder characterized by moderate to severe intellectual disability, delayed growth, hypotonia, seizures, limited speech ability, malformations, hearing and vision impairment, and distinct facial features. The symptoms may vary, depending on the exact location of the chromosomal deletion.The condition is caused by a genetic deletion (loss of a segment of DNA) on the outermost band on the short arm (p) of chromosome 1. It is one of the most common deletion syndromes. It is estimated that the syndrome occurs in one in every 5,000 to 10,000 births. Knowledge of the disorder has increased a great deal over the last decade, mainly because more patients have been accurately diagnosed and described in international medical literature.".
- Q3297103 thumbnail Facial_Features_of_a_Child_with_1p36_Deletion_Syndromel.png?width=300.
- Q3297103 wikiPageExternalLink what-is-1p36-deletion-syndrome.
- Q3297103 wikiPageExternalLink br.fcgi?book=gene&part=del1p36.
- Q3297103 wikiPageExternalLink uk-1p36.pdf.
- Q3297103 wikiPageExternalLink 1p36+deletion+syndrome.htm.
- Q3297103 wikiPageWikiLink Q101065.
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- Q3297103 wikiPageWikiLink Q8280463.
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- Q3297103 comment "1p36 deletion syndrome (also known as monosomy 1p36) is a congenital genetic disorder characterized by moderate to severe intellectual disability, delayed growth, hypotonia, seizures, limited speech ability, malformations, hearing and vision impairment, and distinct facial features. The symptoms may vary, depending on the exact location of the chromosomal deletion.The condition is caused by a genetic deletion (loss of a segment of DNA) on the outermost band on the short arm (p) of chromosome 1.".
- Q3297103 label "1p36 deletion syndrome".
- Q3297103 depiction Facial_Features_of_a_Child_with_1p36_Deletion_Syndromel.png.