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Author/Creator Croft, Brittany

4. FGF9 variant in 46, XY DSD patient suggests a role for dimerization in sex determination. Issue 3 (28th November 2022)

Authors:
Croft, Brittany; Bird, Anthony D.; Ono, Makoto; Eggers, Stefanie; Bagheri‐Fam, Stefan; Ryan, Janelle M.; Reyes, Alejandra P.; van den Bergen, Jocelyn; Baxendale, Anne; Thompson, Elizabeth M.; Kueh, Andrew J.; Stanton, Peter; Thomas, Tim; Sinclair, Andrew H.; Harley, Vincent R.
Journal:
Clinical genetics
Issue:
Volume 103:Issue 3(2023)
Page Start:
277
Record Type:
Journal Article
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6. Mutant NR5A1/SF‐1 in patients with disorders of sex development shows defective activation of the SOX9 TESCO enhancer. Issue 12 (22nd August 2018)

Authors:
Sreenivasan, Rajini; Ludbrook, Louisa; Fisher, Brett; Declosmenil, Faustine; Knower, Kevin C.; Croft, Brittany; Bird, Anthony D.; Ryan, Janelle; Bashamboo, Anu; Sinclair, Andrew H.; Koopman, Peter; McElreavey, Ken; Poulat, Francis; Harley, Vincent R.
Journal:
Human mutation
Issue:
Volume 39:Issue 12(2018)
Page Start:
1861
Record Type:
Journal Article
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7. NR5A1 gene variants repress the ovarian‐specific WNT signaling pathway in 46, XX disorders of sex development patients. Issue 2 (30th November 2018)

Authors:
Knarston, Ingrid M.; Robevska, Gorjana; van den Bergen, Jocelyn A; Eggers, Stefanie; Croft, Brittany; Yates, Jason; Hersmus, Remko; Looijenga, Leendert H. J.; Cameron, Fergus J.; Monhike, Klaus; Ayers, Katie L.; Sinclair, Andrew H.
Journal:
Human mutation
Issue:
Volume 40:Issue 2(2019)
Page Start:
207
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗