Please use this identifier to cite or link to this item:
https://olympias.lib.uoi.gr/jspui/handle/123456789/18985| Title: | Prolonged jaundice and hypothyroidism as the presenting symptoms in a neonate with a novel Prop1 gene mutation (Q83X) |
| Institution and School/Department of submitter: | Πανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικής |
| Keywords: | *Codon, Nonsense,Homeodomain Proteins/*genetics,Human Growth Hormone/deficiency/metabolism,Humans,Hypothyroidism/blood/drug therapy/*genetics,Infant,Jaundice/blood/genetics,Male,Pedigree,Thyrotropin/blood,Thyroxine/blood/therapeutic use,Triiodothyronine/blood |
| URI: | https://olympias.lib.uoi.gr/jspui/handle/123456789/18985 |
| ISSN: | 0804-4643 |
| Link: | http://www.ncbi.nlm.nih.gov/pubmed/15012608 http://www.eje-online.org/content/150/3/257.full.pdf |
| Appears in Collections: | Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά) - ΙΑΤ |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| Voutetakis-2004-Prolonged jaundice a.pdf | 165.81 kB | Adobe PDF | View/Open Request a copy |
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