93 related articles for article (PubMed ID: 21488305)
1. Novel human pathological mutations. Gene symbol: CYP21A2. Disease: adrenal hyperplasia.
Carvalho B; Marques CJ; Carvalho D; Barros A; Carvalho F
Hum Genet; 2010 Apr; 127(4):482-3. PubMed ID: 21488305
[No Abstract] [Full Text] [Related]
2. Novel human pathological mutations. Gene Symbol: CYP21A2. Disease: Non-classic 21-hydroxylase deficiency.
Concolino P; Santonocito C; Minucci A; Carrozza C; Zuppi C; Capoluongo E; Giardina B
Hum Genet; 2007 Dec; 122(5):559. PubMed ID: 18386334
[No Abstract] [Full Text] [Related]
3. Gene symbol: CYP21A2. Disease: adrenal hyperplasia, CYP21.
Dain L; Minutolo C; Buzzalino N; Belli S; Oneto A; Charreau E; Alba L
Hum Genet; 2006 Apr; 119(3):363. PubMed ID: 17230657
[No Abstract] [Full Text] [Related]
4. Gene symbol: CYP21A2. Disease: steroid 21-hydroxylase deficiency.
Tardy V
Hum Genet; 2006 Apr; 119(3):363. PubMed ID: 17230656
[No Abstract] [Full Text] [Related]
5. Gene symbol: CYP21A2. Disease: Adrenal hyperplasia.
Capoluongo E; Concolino P; Carrozza C; Santonocito C; Zuppi C
Hum Genet; 2008 Jun; 123(5):550. PubMed ID: 20960642
[No Abstract] [Full Text] [Related]
6. Gene symbol: CYP21A2. Disease: Adrenal hyperplasia.
Capoluongo E; Concolino P; Vendittelli F; Zuppi C
Hum Genet; 2008 Jun; 123(5):549-50. PubMed ID: 20960641
[No Abstract] [Full Text] [Related]
7. Gene symbol: CYP21A2. Disease: Adrenal hyperplasia.
Capoluongo E; Concolino P; Minucci A; Giardina B
Hum Genet; 2008 Jun; 123(5):550. PubMed ID: 20960643
[No Abstract] [Full Text] [Related]
8. Three novel CYP21A2 mutations and their protein modelling in patients with classical 21-hydroxylase deficiency from northeastern Iran.
Baradaran-Heravi A; Vakili R; Robins T; Carlsson J; Ghaemi N; A'rabi A; Abbaszadegan MR
Clin Endocrinol (Oxf); 2007 Sep; 67(3):335-41. PubMed ID: 17573904
[TBL] [Abstract][Full Text] [Related]
9. A new CYP21A2 nonsense mutation causing severe 21-hydroxylase deficiency.
Concolino P; Minucci A; Mello E; Zuppi C; Capoluongo E
Clin Chem Lab Med; 2009; 47(7):824-5. PubMed ID: 19499972
[TBL] [Abstract][Full Text] [Related]
10. Gene symbol: CYP21A2.
Tardy VT; Morel Y
Hum Genet; 2007 Apr; 121(2):294. PubMed ID: 17598239
[No Abstract] [Full Text] [Related]
11. Gene symbol: CYP21A2.
Tardy VT
Hum Genet; 2007 Apr; 121(2):292-3. PubMed ID: 17598236
[No Abstract] [Full Text] [Related]
12. Gene symbol: CYP21A2.
Tardy VT
Hum Genet; 2007 Apr; 121(2):292. PubMed ID: 17598235
[No Abstract] [Full Text] [Related]
13. Gene symbol: CYP21A2.
Tardy VT
Hum Genet; 2007 Apr; 121(2):293. PubMed ID: 17598208
[No Abstract] [Full Text] [Related]
14. Functional analysis of two rare CYP21A2 mutations detected in Italian patients with a mildest form of congenital adrenal hyperplasia.
Concolino P; Vendittelli F; Mello E; Minucci A; Carrozza C; Rossodivita A; Giardina B; Zuppi C; Capoluongo E
Clin Endocrinol (Oxf); 2009 Oct; 71(4):470-6. PubMed ID: 19170707
[TBL] [Abstract][Full Text] [Related]
15. Gene symbol: CYP21A2.
Tardy VT; Morel Y
Hum Genet; 2007 Apr; 121(2):293-4. PubMed ID: 17598238
[No Abstract] [Full Text] [Related]
16. Gene symbol: CYP21A2.
Tardy VT; Morel Y
Hum Genet; 2007 Apr; 121(2):293. PubMed ID: 17598237
[No Abstract] [Full Text] [Related]
17. Three novel mutations in Japanese patients with 21-hydroxylase deficiency.
Usui T; Nishisho K; Kaji M; Ikuno N; Yorifuji T; Yasuda T; Kuzuya H; Shimatsu A
Horm Res; 2004; 61(3):126-32. PubMed ID: 14676460
[TBL] [Abstract][Full Text] [Related]
18. Molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: an update of new CYP21A2 mutations.
Concolino P; Mello E; Zuppi C; Capoluongo E
Clin Chem Lab Med; 2010 Aug; 48(8):1057-62. PubMed ID: 20482300
[TBL] [Abstract][Full Text] [Related]
19. A previously undescribed mutation detected by sequence analysis of CYP21A2 gene in an infant with salt wasting congenital adrenal hyperplasia.
Girgis R; Ajamian F; Metcalfe P
J Pediatr Endocrinol Metab; 2013; 26(7-8):765-6. PubMed ID: 23907417
[TBL] [Abstract][Full Text] [Related]
20. [Expression of the human steroid 21-hydroxylase gene and its mutant variant C169R in insect cells and functional analysis of expression products].
Grishchuk IuV; Rubtsov PM; Belzhelarskaia SN
Mol Biol (Mosk); 2007; 41(1):71-8. PubMed ID: 17380893
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
