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Quoted phrase not found in phrase index: "46,xx sex reversal 5"
Page 1
Duplication of SOX3 in an SRY-negative 46,XX male with prostatic utricle: case report and literature review.
BMC Med Genomics. 2022 Sep 5;15(1):188. doi: 10.1186/s12920-022-01347-0.
BMC Med Genomics. 2022.
PMID: 36064700
Free PMC article.
Review.
BACKGROUND: 46,XX male disorders of sex development are rare. Approximately 80% of cases of testicular tissue differentiation may be due to translocation of SRY to the X chromosome or an autosome. ...SOX3 duplication may cause sex reversal, and …
BACKGROUND: 46,XX male disorders of sex development are rare. Approximately 80% of cases of testicular tissue different …
Livebirth after uterus transplantation.
Brännström M, Johannesson L, Bokström H, Kvarnström N, Mölne J, Dahm-Kähler P, Enskog A, Milenkovic M, Ekberg J, Diaz-Garcia C, Gäbel M, Hanafy A, Hagberg H, Olausson M, Nilsson L.
Brännström M, et al.
Lancet. 2015 Feb 14;385(9968):607-616. doi: 10.1016/S0140-6736(14)61728-1. Epub 2014 Oct 6.
Lancet. 2015.
PMID: 25301505
The patient was admitted with pre-eclampsia at 31 full weeks and 5 days, and 16 h later a caesarean section was done because of abnormal cardiotocography. A male baby with a normal birthweight for gestational age (1775 g) and with APGAR scores 9, 9, 10 was born. INT …
The patient was admitted with pre-eclampsia at 31 full weeks and 5 days, and 16 h later a caesarean section was done because of abnor …
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A novel germ line mutation in SOX9 causes familial campomelic dysplasia and sex reversal.
Cameron FJ, Hageman RM, Cooke-Yarborough C, Kwok C, Goodwin LL, Sillence DO, Sinclair AH.
Cameron FJ, et al.
Hum Mol Genet. 1996 Oct;5(10):1625-30. doi: 10.1093/hmg/5.10.1625.
Hum Mol Genet. 1996.
PMID: 8894698
Consequently, CD and autosomal sex reversal may result from haploinsufficiency of SOX9. The SOX9 gene maps to the long arm of human chromosome 17 and translocations in this region also result in CD. ...The proband was found to have 46,XY true hermaphroditism with am …
Consequently, CD and autosomal sex reversal may result from haploinsufficiency of SOX9. The SOX9 gene maps to the long arm of …
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Prenatal diagnosis of sex differentiation disorders: the role of fetal ultrasound.
Pinhas-Hamiel O, Zalel Y, Smith E, Mazkereth R, Aviram A, Lipitz S, Achiron R.
Pinhas-Hamiel O, et al.
J Clin Endocrinol Metab. 2002 Oct;87(10):4547-53. doi: 10.1210/jc.2001-011034.
J Clin Endocrinol Metab. 2002.
PMID: 12364433
Over a 5-yr period all cases suspected of sexual ambiguity based on abnormal ultrasonographic scans (US) or US/genotype US discrepancy were evaluated prenatally by three modalities: 1) repeated fetal US; 2) genetic studies, primarily karyotype and fluorescence in situ hybr …
Over a 5-yr period all cases suspected of sexual ambiguity based on abnormal ultrasonographic scans (US) or US/genotype US discrepanc …
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