Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Sólveig Oskarsdóttir"'
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100141- (2023)
Externí odkaz:
https://doaj.org/article/0392ef656f684a1ba67521b677c91148
Autor:
Jenny Lingman Framme, Christina Lundqvist, Anna-Carin Lundell, Pauline A. van Schouwenburg, Andri L. Lemarquis, Karolina Thörn, Susanne Lindgren, Judith Gudmundsdottir, Vanja Lundberg, Sofie Degerman, Rolf H. Zetterström, Stephan Borte, Lennart Hammarström, Esbjörn Telemo, Magnus Hultdin, Mirjam van der Burg, Anders Fasth, Sólveig Oskarsdóttir, Olov Ekwall
Publikováno v:
Journal of Clinical Immunology, 42, 618-633. SPRINGER/PLENUM PUBLISHERS
Background Population-based neonatal screening using T-cell receptor excision circles (TRECs) identifies infants with profound T lymphopenia, as seen in cases of severe combined immunodeficiency, and in a subgroup of infants with 22q11 deletion syndr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56a75d5bd7e741da61caee4f8e2ce768
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-192261
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-192261
Publikováno v:
International journal of paediatric dentistry. 20(4)
22q11 deletion syndrome (22q11DS) is one of the most common multiple anomaly syndromes, and many dentists are likely to meet patients with the syndrome. Odontological research has focused on describing and analysing conditions/concepts based on the c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::97ba1007e450910a1094bf120e892ba5
https://pubmed.ncbi.nlm.nih.gov/20536590
https://pubmed.ncbi.nlm.nih.gov/20536590
Publikováno v:
Pediatric hematology and oncology. 8(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d28fbf179de33a070c47d637c1f940b8
https://pubmed.ncbi.nlm.nih.gov/1742187
https://pubmed.ncbi.nlm.nih.gov/1742187