1 |
Jacobs PA, Baikie AG, Brown WM, et al. Evidence for the existence of the human "super female"[J]. Lancet, 1959, 2(7100): 423-425.
|
2 |
Berglund A, Viuff MH, Skakkebæk A, et al. Changes in the cohort composition of Turner syndrome and severe non-diagnosis of Klinefelter, 47,XXX and 47,XYY syndrome: a nationwide cohort study[J]. Orphanet J Rare Dis, 2019, 14(1): 16.
|
3 |
Li M, Zou C, Zhao Z. Triple X syndrome with short stature: case report and literature review[J]. Iran J Pediatr, 2012, 22(2): 269-273.
|
4 |
梁雁, 杜敏联, 罗小平. 中枢性性早熟诊断与治疗共识(2015)[J]. 中华儿科杂志, 2015, 53(6): 412-418.
|
5 |
李辉, 季成叶, 宗心南, 等.中国0~18岁儿童、青少年身高、体重的标准化生长曲线[J].中华儿科杂志, 2009, 47(7): 487-492.
|
6 |
Stochholm K, Juul S, Gravholt CH. Mortality and incidence in women with 47,XXX and variants[J]. Am J Med Genet A, 2010, 152A(2): 367-372.
|
7 |
郭利丽, 丁建林, 贾静, 等. 47,XXX综合征的研究进展[J]. 国际生殖健康/计划生育杂志, 2020, 39(1): 49-53.
|
8 |
Yamazaki S, Akutsu Y, Shimbo A, et al. Childhood-onset systemic lupus erythematosus with trisomy X and the increased risk for bone complications: a case report[J]. Pediatr Rheumatol Online J, 2021, 19(1): 20.
|
9 |
Rafique M, AlObaid S, Al-Jaroudi D. 47,XXX syndrome with infertility, premature ovarian insufficiency, and streak ovaries[J]. Clin Case Rep, 2019, 7(6): 1238-1241.
|
10 |
Vogt PH, Affara N, Davey P, et al. Report of the third international workshop on Y chromosome mapping 1997. Heidelberg, Germany, April 13-16, 1997[J]. Cytogenet Cell Genet, 1997, 79(1-2): 1-20.
|
11 |
Nielsen MM, Trolle C, Vang S, et al. Epigenetic and transcriptomic consequences of excess X-chromosome material in 47,XXX syndrome: a comparison with Turner syndrome and 46,XX females[J]. Am J Med Genet C Semin Med Genet, 2020,184(2):279-293.
|
12 |
Aksglaede L, Skakkebaek NE, Juul A. Abnormal sex chromosome constitution and longitudinal growth: serum levels of insulin-like growth factor (IGF)-I, IGF binding protein-3, luteinizing hormone, and testosterone in 109 males with 47,XXY, 47,XYY, or sex-determining region of the Y chromosome (SRY)-positive 46,XX karyotypes[J]. J Clin Endocrinol Metab,2008, 93(1):169-176.
|
13 |
Ogata T, Matsuo N. Sex chromosome aberrations and stature: deduction of the principal factors involved in the determination of adult height[J]. Hum Genet, 1993, 91(6): 551-562.
|
14 |
Stagi S, Di Tommaso M, Scalini P, et al. Cross-sectional study shows that impaired bone mineral status and metabolism are found in nonmosaic triple X syndrome[J]. Acta Paediatr, 2017, 106(4): 619-626.
|
15 |
Frederiksen AL, Hansen S, Brixen K, et al. Increased cortical area and thickness in the distal radius in subjects with SHOX-gene mutation[J]. Bone, 2014, 69: 23-29.
|
16 |
Butnariu L, Rusu C, Caba L, et al. Genotype- phenotype correlation in trisomy X: a retrospective study of a selected group of 36 patients and review of literature[J]. Rev Med Chir Soc Med Nat Iasi, 2013, 117(3): 714-721.
|
17 |
Wallerstein R, Musen E, McCarrier J, et al. Turner syndrome phenotype with 47,XXX karyotype: further investigation warranted? [J]. Am J Med Genet A, 2004, 125A(1): 106-107.
|
18 |
Davis SM, Soares K, Howell S, et al. Diminished ovarian reserve in girls and adolescents with trisomy X syndrome[J]. Reprod Sci, 2020, 27(11): 1985-1991.
|
19 |
Sybert VP. Phenotypic effects of mosaicism for a 47,XXX cell line in Turner syndrome[J]. J Med Genet, 2002, 39(3): 217-220.
|