Concolino P, Falhammar H
J Endocr Soc. 2025; 9(3):bvaf018.
PMID: 39911519
PMC: 11795198.
DOI: 10.1210/jendso/bvaf018.
Nokoff N, Buchanan C, Barker J
J Clin Endocrinol Metab. 2025; 110(Supplement_1):S13-S24.
PMID: 39836622
PMC: 11749889.
DOI: 10.1210/clinem/dgae563.
Yang M, White P
J Clin Endocrinol Metab. 2025; 110(Supplement_1):S1-S12.
PMID: 39836621
PMC: 11749890.
DOI: 10.1210/clinem/dgae535.
Wang Y, Zhu G, Li D, Pan Y, Li R, Zhou T
Hum Genomics. 2025; 19(1):3.
PMID: 39810276
PMC: 11731552.
DOI: 10.1186/s40246-024-00696-4.
Chen X, Zhao J, Li D, Xi N, Yi D, Yan M
Mol Genet Genomic Med. 2024; 12(11):e70029.
PMID: 39575462
PMC: 11582476.
DOI: 10.1002/mgg3.70029.
Comparison of long-read sequencing and MLPA combined with long-PCR sequencing of mutations in patients with 21-OHD.
Lan T, Wang J, Chen K, Zhang J, Chen X, Yao H
Front Genet. 2024; 15:1472516.
PMID: 39553475
PMC: 11563783.
DOI: 10.3389/fgene.2024.1472516.
Genomic complexity and clinical significance of the RCCX locus.
Shiryagin V, Devyatkin A, Fateev O, Petriaikina E, Bogdanov V, Antysheva Z
PeerJ. 2024; 12:e18243.
PMID: 39512309
PMC: 11542561.
DOI: 10.7717/peerj.18243.
Congenital Adrenal Hyperplasia - A Comprehensive Review of Genetic Studies on 21-Hydroxylase Deficiency from India.
Ravichandran L, Asha H, Mathai S, Thomas N, Chapla A
Indian J Endocrinol Metab. 2024; 28(2):117-128.
PMID: 38911104
PMC: 11189293.
DOI: 10.4103/ijem.ijem_303_23.
Gene Analysis in Southern Iranian CAH Patients and a Brief Review of the Mutation Spectrum.
Zangene D, Moravej H, Ilkhanipoor H, Amirhakimi A, Afshar Z, Entezam M
Avicenna J Med Biotechnol. 2024; 16(2):130-135.
PMID: 38618509
PMC: 11007372.
DOI: 10.18502/ajmb.v16i2.14864.
Genetic Characterization of a Cohort of Italian Patients with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency.
Concolino P, Perrucci A, Carrozza C, Urbani A
Mol Diagn Ther. 2023; 27(5):621-630.
PMID: 37548905
DOI: 10.1007/s40291-023-00666-x.
Molecular basis and genetic testing strategies for diagnosing 21-hydroxylase deficiency, including CAH-X syndrome.
Kim J, Kim G, Yoo H, Choi J
Ann Pediatr Endocrinol Metab. 2023; 28(2):77-86.
PMID: 37401054
PMC: 10329939.
DOI: 10.6065/apem.2346108.054.
The underlying cause of the simple virilizing phenotype in patients with 21-hydroxylase deficiency harboring P31L variant.
Zhao Z, Gao Y, Lu L, Tong A, Chen S, Zhang W
Front Endocrinol (Lausanne). 2023; 13:1015773.
PMID: 36866166
PMC: 9972294.
DOI: 10.3389/fendo.2022.1015773.
History of Adrenal Research: From Ancient Anatomy to Contemporary Molecular Biology.
Miller W, White P
Endocr Rev. 2022; 44(1):70-116.
PMID: 35947694
PMC: 9835964.
DOI: 10.1210/endrev/bnac019.
Gene Expression in a Humanized 21-Hydroxylase Mouse Model Does Not Affect Adrenocortical Morphology and Function.
Schubert T, Reisch N, Naumann R, Reichardt I, Landgraf D, Quitter F
J Endocr Soc. 2022; 6(6):bvac062.
PMID: 35592511
PMC: 9113096.
DOI: 10.1210/jendso/bvac062.
Congenital Adrenal Hyperplasia and Ehlers-Danlos Syndrome.
Marino R, Moresco A, Perez Garrido N, Ramirez P, Belgorosky A
Front Endocrinol (Lausanne). 2022; 13:803226.
PMID: 35282436
PMC: 8913572.
DOI: 10.3389/fendo.2022.803226.
Characteristics of In2G Variant in Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency.
Kocova M, Concolino P, Falhammar H
Front Endocrinol (Lausanne). 2022; 12:788812.
PMID: 35140681
PMC: 8818746.
DOI: 10.3389/fendo.2021.788812.
Recurrent pneumothorax in a case of tenascin-X deficient Ehlers-Danlos syndrome: Broadening the phenotypic spectrum.
Santoreneos R, Vakulin C, Ellul M, Rawlings L, Hardy T, Poplawski N
Am J Med Genet A. 2022; 188(5):1583-1588.
PMID: 35128805
PMC: 9303620.
DOI: 10.1002/ajmg.a.62674.
2+0 deletion carrier - a limitation of the genetic testing and counseling: A case report.
Xi N, Song X, Wang X, Qin S, He G, Sun L
World J Clin Cases. 2021; 9(23):6789-6797.
PMID: 34447826
PMC: 8362542.
DOI: 10.12998/wjcc.v9.i23.6789.
Genes and Pseudogenes: Complexity of the RCCX Locus and Disease.
Carrozza C, Foca L, De Paolis E, Concolino P
Front Endocrinol (Lausanne). 2021; 12:709758.
PMID: 34394006
PMC: 8362596.
DOI: 10.3389/fendo.2021.709758.
Genotypic spectrum of 21-hydroxylase deficiency in an endogamous population.
Mahmoud R, Amr N, Toaima N, Kamal T, Elsedfy H
J Endocrinol Invest. 2021; 45(2):347-359.
PMID: 34341969
DOI: 10.1007/s40618-021-01648-8.