161 related articles for article (PubMed ID: 38481442)
1. Evaluating the relationship between the proportion of X-chromosome deletions and clinical manifestations in children with turner syndrome.
Wang G; Liu X; Wang M; Wang J; Zhang Z; Allegaert K; Mei D; Zhang Y; Luo S; Fang Y; Li D; Chen Y; Wei H
Front Endocrinol (Lausanne); 2024; 15():1324160. PubMed ID: 38481442
[TBL] [Abstract][Full Text] [Related]
2. [Application of fluorescence in situ hybridization combined with chromosomal karyotyping analysis in children with disorders of sex development due to sex chromosome abnormalities].
Wang G; Wang J; Zhang Z; Li R; Li L; Li D; Zhang W; Zhang Y; Wang M
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Aug; 40(8):947-953. PubMed ID: 37532493
[TBL] [Abstract][Full Text] [Related]
3. Left-sided congenital heart lesions in mosaic Turner syndrome.
Bouayed Abdelmoula N; Abdelmoula B; Smaoui W; Trabelsi I; Louati R; Aloulou S; Aloulou W; Abid F; Kammoun S; Trigui K; Bedoui O; Denguir H; Mallek S; Ben Aziza M; Dammak J; Kaabi O; Abdellaoui N; Turki F; Kaabi A; Kamoun W; Jabeur J; Ltaif W; Chaker K; Fourati H; M'rabet S; Ben Ameur H; Gouia N; Mhiri MN; Rebai T
Mol Genet Genomics; 2018 Apr; 293(2):495-501. PubMed ID: 29196848
[TBL] [Abstract][Full Text] [Related]
4. X chromosome gene dosage as a determinant of congenital malformations and of age-related comorbidity risk in patients with Turner syndrome, from childhood to early adulthood.
Fiot E; Zénaty D; Boizeau P; Haignere J; Dos Santos S; Léger J;
Eur J Endocrinol; 2019 Jun; 180(6):397-406. PubMed ID: 30991358
[TBL] [Abstract][Full Text] [Related]
5. Ovarian reserve evaluation in a woman with 45,X/47,XXX mosaicism: A case report and a review of literature.
Tang R; Lin L; Guo Z; Hou H; Yu Q
Mol Genet Genomic Med; 2019 Jul; 7(7):e00732. PubMed ID: 31070017
[TBL] [Abstract][Full Text] [Related]
6. Genetic considerations in the patient with Turner syndrome--45,X with or without mosaicism.
Zhong Q; Layman LC
Fertil Steril; 2012 Oct; 98(4):775-9. PubMed ID: 23020909
[TBL] [Abstract][Full Text] [Related]
7. Molecular diagnosis of Turner's syndrome.
Gicquel C; Cabrol S; Schneid H; Girard F; Le Bouc Y
J Med Genet; 1992 Aug; 29(8):547-51. PubMed ID: 1355559
[TBL] [Abstract][Full Text] [Related]
8. Gene dosage as a relevant mechanism contributing to the determination of ovarian function in Turner syndrome.
Castronovo C; Rossetti R; Rusconi D; Recalcati MP; Cacciatore C; Beccaria E; Calcaterra V; Invernizzi P; Larizza D; Finelli P; Persani L
Hum Reprod; 2014 Feb; 29(2):368-79. PubMed ID: 24324027
[TBL] [Abstract][Full Text] [Related]
9. Hidden Y Chromosome Material and Congenital Cardiovascular Malformations in a Cohort of Turner Syndrome Patients with 45,X Blood Karyotype.
Udo EQ; Truly T; Peters A; Prakash SK; Rivera M; Rodriguez-Buritica DF
Cytogenet Genome Res; 2023; 163(5-6):290-294. PubMed ID: 38128492
[TBL] [Abstract][Full Text] [Related]
10. Molecular cytogenetic characterization of two Turner syndrome patients with mosaic ring X chromosome.
Chauhan P; Jaiswal SK; Lakhotia AR; Rai AK
J Assist Reprod Genet; 2016 Sep; 33(9):1161-8. PubMed ID: 27387888
[TBL] [Abstract][Full Text] [Related]
11. Bicuspid aortic valve and aortic coarctation are linked to deletion of the X chromosome short arm in Turner syndrome.
Bondy C; Bakalov VK; Cheng C; Olivieri L; Rosing DR; Arai AE
J Med Genet; 2013 Oct; 50(10):662-5. PubMed ID: 23825392
[TBL] [Abstract][Full Text] [Related]
12. Increased prevalence of bicuspid aortic valve in Turner syndrome links with karyotype: the crucial importance of detailed cardiovascular screening.
Klásková E; Zapletalová J; Kaprálová S; Šnajderová M; Lebl J; Tüdös Z; Pavlíček J; Černá J; Mihál V; Stará V; Procházka M
J Pediatr Endocrinol Metab; 2017 Mar; 30(3):319-325. PubMed ID: 28236629
[TBL] [Abstract][Full Text] [Related]
13. Chromosomal mosaicism mitigates stigmata and cardiovascular risk factors in Turner syndrome.
El-Mansoury M; Barrenäs ML; Bryman I; Hanson C; Larsson C; Wilhelmsen L; Landin-Wilhelmsen K
Clin Endocrinol (Oxf); 2007 May; 66(5):744-51. PubMed ID: 17381484
[TBL] [Abstract][Full Text] [Related]
14. [Genetic analysis of Turner syndrome: 89 cases in Tunisia].
Kammoun I; Chaabouni M; Trabelsi M; Ouertani I; Kraoua L; Chelly I; M'rad R; Ben Jemaa L; Maâzoul F; Chaabouni H
Ann Endocrinol (Paris); 2008 Nov; 69(5):440-5. PubMed ID: 18541220
[TBL] [Abstract][Full Text] [Related]
15. Buccal cell FISH and blood PCR-Y detect high rates of X chromosomal mosaicism and Y chromosomal derivatives in patients with Turner syndrome.
Freriks K; Timmers HJ; Netea-Maier RT; Beerendonk CC; Otten BJ; van Alfen-van der Velden JA; Traas MA; Mieloo H; van de Zande GW; Hoefsloot LH; Hermus AR; Smeets DF
Eur J Med Genet; 2013 Sep; 56(9):497-501. PubMed ID: 23933507
[TBL] [Abstract][Full Text] [Related]
16. An atypical Turner syndrome patient with ring X chromosome mosaicism.
Cantú ES; Jacobs DF; Pai GS
Ann Clin Lab Sci; 1995; 25(1):60-5. PubMed ID: 7762970
[TBL] [Abstract][Full Text] [Related]
17. Assessment of Turner's syndrome by molecular analysis of the X chromosome in growth-retarded girls.
Gicquel C; Gaston V; Cabrol S; Le Bouc Y
J Clin Endocrinol Metab; 1998 May; 83(5):1472-6. PubMed ID: 9589641
[TBL] [Abstract][Full Text] [Related]
18. Turner syndrome female with a small ring X chromosome lacking the XIST, an unexpectedly mild phenotype and an atypical association with alopecia universalis.
Bouayed Abdelmoula N; Portnoï MF; Amouri A; Arladan A; Chakroun M; Saad A; Hchicha M; Turki H; Rebai T
Ann Genet; 2004; 47(3):305-13. PubMed ID: 15337477
[TBL] [Abstract][Full Text] [Related]
19. Gonadoblastoma in Turner syndrome patients with nonmosaic 45,X karyotype and Y chromosome sequences.
Canto P; Kofman-Alfaro S; Jiménez AL; Söderlund D; Barrón C; Reyes E; Méndez JP; Zenteno JC
Cancer Genet Cytogenet; 2004 Apr; 150(1):70-2. PubMed ID: 15041227
[TBL] [Abstract][Full Text] [Related]
20. The proportion of diploid 46,XX cells increases with time in women with Turner syndrome--a 10-year follow-up study.
Denes AM; Landin-Wilhelmsen K; Wettergren Y; Bryman I; Hanson C
Genet Test Mol Biomarkers; 2015 Feb; 19(2):82-7. PubMed ID: 25587646
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
