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Author/Creator Lundin, Johanna

1. Copy number variants suggest different molecular pathways for the pathogenesis of bladder exstrophy. Issue 2 (8th November 2022)

Authors:
Nordenskjöld, Agneta; Arkani, Samara; Pettersson, Maria; Winberg, Johanna; Cao, Jia; Fossum, Magdalena; Anderberg, Magnus; Barker, Gillian; Holmdahl, Gundela; Lundin, Johanna
Journal:
American journal of medical genetics
Issue:
Volume 191:Issue 2(2023)
Page Start:
378
Record Type:
Journal Article
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2. Further molecular and clinical delineation of co-locating 17p13.3 microdeletions and microduplications that show distinctive phenotypes. Issue 5 (7th May 2010)

Authors:
Bruno, Damien L; Anderlid, Britt-Marie; Lindstrand, Anna; van Ravenswaaij-Arts, Conny; Ganesamoorthy, Devika; Lundin, Johanna; Martin, Christa Lese; Douglas, Jessica; Nowak, Catherine; Adam, Margaret P; Kooy, R Frank; Van der Aa, Nathalie; Reyniers, Edwin; Vandeweyer, Geert; Stolte-Dijkstra, Iren...
Journal:
Journal of medical genetics
Issue:
Volume 47:Issue 5(2010)
Page Start:
299
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. Further support linking the 22q11.2 microduplication to an increased risk of bladder exstrophy and highlighting LZTR1 as a candidate gene. Issue 6 (1st May 2019)

Authors:
Lundin, Johanna; Markljung, Ellen; Baranowska Körberg, Izabella; Hofmeister, Wolfgang; Cao, Jia; Nilsson, Daniel; Holmdahl, Gundela; Barker, Gillian; Anderberg, Magnus; Vukojević, Vladana; Lindstrand, Anna; Nordenskjöld, Agneta
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 7:Issue 6(2019)
Page Start:
n/a
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗