128 related articles for article (PubMed ID: 37906155)
1. [Genetic analysis of a rare case with Disorder of sex development due to structural rearrangement of Y chromosome].
Mi M; Xia J; Hou Y; Dai P; Wang Y; Kong X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Nov; 40(11):1430-1435. PubMed ID: 37906155
[TBL] [Abstract][Full Text] [Related]
2. [Clinical and genetic characteristic in patients with disorders of sex development caused by Y chromosome copy number variant].
Xia JK; Tian FY; Hou YQ; Zhao YJ; Kong XD
Zhonghua Er Ke Za Zhi; 2023 May; 61(5):459-463. PubMed ID: 37096267
[No Abstract] [Full Text] [Related]
3. [Prenatal diagnosis for two fetuses carrying partial deletion of Y chromosome].
Pang H; Gao M; Hua J; Tong D; Zhao Y; Feng X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Feb; 37(2):182-185. PubMed ID: 32034751
[TBL] [Abstract][Full Text] [Related]
4. [Genetic analysis for a female carrying idic(Y)(p11.32) with Disorders of sex development].
Zhang Y; Xu Z; Zhao X; Li L
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 May; 41(5):626-631. PubMed ID: 38684314
[TBL] [Abstract][Full Text] [Related]
5. [Genetic analysis of a fetus with mosaicism Y chromosome aberration].
Meng F; Ju D; Wang X; Shi Y; Yang M; Li X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Nov; 40(11):1414-1419. PubMed ID: 37906152
[TBL] [Abstract][Full Text] [Related]
6. Hypospadias in a male infant with an unusual mosaic 45,X/46,X,psu idic(Y)(p11.32)/46,XY and haploinsufficiency of SHOX: A case report.
Si YM; Dong Y; Wang W; Qi KY; Wang X
Mol Med Rep; 2017 Jul; 16(1):201-207. PubMed ID: 28498391
[TBL] [Abstract][Full Text] [Related]
7. [Application of low-depth whole genome sequencing for copy number variation analysis in children with disorders of sex development].
Xia J; Hou Y; Dai P; Zhao Z; Chen C; Kong X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Feb; 40(2):195-201. PubMed ID: 36709940
[TBL] [Abstract][Full Text] [Related]
8. A mosaic karyotype of 45,X/46,X,psu idic(Y)(q12) in a ten-year-old boy: integrating high-throughput sequencing with cytogenetic technique for precise diagnosis and genetic counselling.
Yin H; Xie H; Zou J; Ye X; Liu Y; He C; Shangguan S; Liu H; Chen X; Chen X
BMC Pediatr; 2023 Mar; 23(1):104. PubMed ID: 36870983
[TBL] [Abstract][Full Text] [Related]
9. [Delineation of three structural Y chromosome aberrations combined molecular techniques].
Tu XD; Zeng J; Cong XW; Yan AZ; Huang WJ; Lin YH; Zheng DZ; Zhang M; Wang ZH
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Aug; 30(4):420-4. PubMed ID: 23926008
[TBL] [Abstract][Full Text] [Related]
10. [Genetic analysis of a fetus with mosaicism of structural aberration of Y chromosome].
Xing H; Yang K
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Dec; 38(12):1250-1253. PubMed ID: 34839518
[TBL] [Abstract][Full Text] [Related]
11. [Genetic analysis of three children with disorders of sex development caused by structural rearrangements of Y chromosome].
Wang H; Chen L; Chen Y; Shen Y; Li L; Shao X; Li H
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Nov; 37(11):1226-1232. PubMed ID: 33179226
[TBL] [Abstract][Full Text] [Related]
12. [Prenatal diagnosis of two fetuses with de novo 46,X,psu dic(Y)/45,X mosaicism].
Chen J; Chen X; Cai M; Zhang J; Ge Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Sep; 37(9):1036-1038. PubMed ID: 32820525
[TBL] [Abstract][Full Text] [Related]
13. [Genetic analysis of a case with mosaicism complex structural aberration of chromosome 18].
Shao M; Yan Z; Zhu X; Yan L; Qiao J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 Jan; 41(1):101-105. PubMed ID: 38171568
[TBL] [Abstract][Full Text] [Related]
14. Detailed analysis of an idic(Y)(q11.21) in a mosaic karyotype.
Al-Achkar W; Wafa A; Liehr T; Klein E; Moassass F
Mol Med Rep; 2012 Aug; 6(2):293-6. PubMed ID: 22664581
[TBL] [Abstract][Full Text] [Related]
15. 45, X/ 46, X, psu idic (Y) (q11.2) Mosaicism in a Primary Amenorrhea Girl with Swyer Syndrome.
Han Y; Wu J; Tan F; Sha J; Zhang B; Zhai J; Wang X
Case Rep Genet; 2023; 2023():9127512. PubMed ID: 36938529
[TBL] [Abstract][Full Text] [Related]
16. Translocation (Y;22) resulting in the loss of SHOX and isolated short stature.
Borie C; Léger J; Dupuy O; Hassan M; Ledu N; Lebbar A; Czernichow P; Eydoux P
Am J Med Genet A; 2004 Mar; 125A(2):186-90. PubMed ID: 14981722
[TBL] [Abstract][Full Text] [Related]
17. Prenatal genetic testing in 19 fetuses with corpus callosum abnormality.
She Q; Tang E; Peng C; Wang L; Wang D; Tan W
J Clin Lab Anal; 2021 Nov; 35(11):e23971. PubMed ID: 34569664
[TBL] [Abstract][Full Text] [Related]
18. Isodicentric Y chromosomes in Egyptian patients with disorders of sex development (DSD).
Mekkawy M; Kamel A; El-Ruby M; Mohamed A; Essawi M; Soliman H; Dessouky N; Shehab M; Mazen I
Am J Med Genet A; 2012 Jul; 158A(7):1594-603. PubMed ID: 22628100
[TBL] [Abstract][Full Text] [Related]
19. A point mutation, R59G, within the HMG-SRY box in a female 45,X/46,X, psu dic(Y)(pter-->q11::q11-->pter).
Fernandez R; Marchal JA; Sanchez A; Pasaro E
Hum Genet; 2002 Sep; 111(3):242-6. PubMed ID: 12215836
[TBL] [Abstract][Full Text] [Related]
20. Unusual maternal uniparental isodisomic x chromosome mosaicism with asymmetric y chromosomal rearrangement.
Lee BY; Kim SY; Park JY; Choi EY; Kim DJ; Kim JW; Ryu HM; Cho YH; Park SY; Seo JT
Cytogenet Genome Res; 2014; 142(2):79-86. PubMed ID: 24434812
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]