Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2014 1
2016 1
2017 1
2018 2
2019 4
2020 2
2021 5
2022 2
2023 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

17 results

Results by year

Filters applied: . Clear all
Quoted phrase not found in phrase index: "Sex chromosome disorder of sex development"
Page 1
Gender identity disorder (GID) in adolescents and adults with differences of sex development (DSD): A systematic review and meta-analysis.
Babu R, Shah U. Babu R, et al. J Pediatr Urol. 2021 Feb;17(1):39-47. doi: 10.1016/j.jpurol.2020.11.017. Epub 2020 Nov 12. J Pediatr Urol. 2021. PMID: 33246831 Review.
Gender assignment in infants born with a difference in sexual development (DSD) remains one of the many difficult decisions faced by the multi-disciplinary treatment team as some of these children develop gender identity disorder (GID) when they become adults …
Gender assignment in infants born with a difference in sexual development (DSD) remains one of the many difficult decisions fa …
Genomics-based non-invasive prenatal testing for detection of fetal chromosomal aneuploidy in pregnant women.
Badeau M, Lindsay C, Blais J, Nshimyumukiza L, Takwoingi Y, Langlois S, Légaré F, Giguère Y, Turgeon AF, Witteman W, Rousseau F. Badeau M, et al. Cochrane Database Syst Rev. 2017 Nov 10;11(11):CD011767. doi: 10.1002/14651858.CD011767.pub2. Cochrane Database Syst Rev. 2017. PMID: 29125628 Free PMC article. Review.
AUTHORS' CONCLUSIONS: These results show that MPSS and TMPS perform similarly in terms of clinical sensitivity and specificity for the detection of fetal T31, T18, T13 and sex chromosome aneuploidy (SCA). However, no study compared the two approaches head-to-head in …
AUTHORS' CONCLUSIONS: These results show that MPSS and TMPS perform similarly in terms of clinical sensitivity and specificity for the detec …
Navigating Disrupted Puberty: Development and Evaluation of a Mobile-Health Transition Passport for Klinefelter Syndrome.
Dwyer AA, Héritier V, Llahana S, Edelman L, Papadakis GE, Vaucher L, Pitteloud N, Hauschild M. Dwyer AA, et al. Front Endocrinol (Lausanne). 2022 Jun 24;13:909830. doi: 10.3389/fendo.2022.909830. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 35813640 Free PMC article.
In conclusion, many patients with KS appear to have gaps in transition to adult-oriented care. Iterative development of a KS transition passport produced a mobile health tool that was usable, understandable and had high ratings for actionability....
In conclusion, many patients with KS appear to have gaps in transition to adult-oriented care. Iterative development of a KS transiti …
Systematic review of quality of life in Turner syndrome.
Reis CT, de Assumpção MS, Guerra-Junior G, de Lemos-Marini SHV. Reis CT, et al. Qual Life Res. 2018 Aug;27(8):1985-2006. doi: 10.1007/s11136-018-1810-y. Epub 2018 Feb 9. Qual Life Res. 2018. PMID: 29427215
Effect of Y Chromosome Microdeletions on the Pregnancy Outcome of Assisted Reproduction Technology: a Meta-analysis.
Li X, Li X, Sun Y, Han J, Ma H, Sun Y. Li X, et al. Reprod Sci. 2021 Sep;28(9):2413-2421. doi: 10.1007/s43032-020-00387-0. Epub 2021 Jan 6. Reprod Sci. 2021. PMID: 33409872
This systematic analysis aimed to summarize the effects of Y chromosome microdeletions (YCMs) on pregnancy outcomes of assisted reproductive technology (ART). ...
This systematic analysis aimed to summarize the effects of Y chromosome microdeletions (YCMs) on pregnancy outcomes of assisted repro …
Depression in Turner Syndrome: A Systematic Review.
Morris LA, Tishelman AC, Kremen J, Ross RA. Morris LA, et al. Arch Sex Behav. 2020 Feb;49(2):769-786. doi: 10.1007/s10508-019-01549-1. Epub 2019 Oct 9. Arch Sex Behav. 2020. PMID: 31598804 Free PMC article.
Y chromosome b2/b3 deletions and male infertility: A comprehensive meta-analysis, trial sequential analysis and systematic review.
Bansal SK, Gupta G, Rajender S. Bansal SK, et al. Mutat Res Rev Mutat Res. 2016 Apr-Jun;768:78-90. doi: 10.1016/j.mrrev.2016.04.007. Epub 2016 May 4. Mutat Res Rev Mutat Res. 2016. PMID: 27234565 Review.
The correlation of Y-chromosome b2/b3 partial deletions with spermatogenic failure remains dubious. ...Further meta-analysis on studies grouped by ethnicity and geographic regions showed that the b2/b3 deletions are significantly associated with spermatogenic loss/infertil …
The correlation of Y-chromosome b2/b3 partial deletions with spermatogenic failure remains dubious. ...Further meta-analysis on studi …
Non-invasive prenatal testing for the prenatal screening of sex chromosome aneuploidies: A systematic review and meta-analysis of diagnostic test accuracy studies.
Soukkhaphone B, Lindsay C, Langlois S, Little J, Rousseau F, Reinharz D. Soukkhaphone B, et al. Mol Genet Genomic Med. 2021 May;9(5):e1654. doi: 10.1002/mgg3.1654. Epub 2021 Mar 23. Mol Genet Genomic Med. 2021. PMID: 33755350 Free PMC article.
BACKGROUND: There is little evidence on the performance of non-invasive prenatal testing (NIPT) for the detection of fetal sex chromosomal imbalances. In this review, we aimed to appraise and synthesize the literature on the performance of NIPT for the prenatal detection o …
BACKGROUND: There is little evidence on the performance of non-invasive prenatal testing (NIPT) for the detection of fetal sex chromo …
Neuropsychiatric decompensation in adolescents and adults with Phelan-McDermid syndrome: a systematic review of the literature.
Kolevzon A, Delaby E, Berry-Kravis E, Buxbaum JD, Betancur C. Kolevzon A, et al. Mol Autism. 2019 Dec 24;10:50. doi: 10.1186/s13229-019-0291-3. eCollection 2019. Mol Autism. 2019. PMID: 31879555 Free PMC article.
Phelan-McDermid syndrome (PMS) is caused by haploinsufficiency of the SHANK3 gene on chromosome 22q13.33 and is characterized by intellectual disability, hypotonia, severe speech impairments, and autism spectrum disorder. ...There were no apparent sex differe …
Phelan-McDermid syndrome (PMS) is caused by haploinsufficiency of the SHANK3 gene on chromosome 22q13.33 and is characterized by inte …
17 results