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For: Murdock DR, Donovan FX, Chandrasekharappa SC, Banks N, Bondy C, Muenke M, Kruszka P. Whole-Exome Sequencing for Diagnosis of Turner Syndrome: Toward Next-Generation Sequencing and Newborn Screening. J Clin Endocrinol Metab 2017;102:1529-37. [PMID: 28324009 DOI: 10.1210/jc.2016-3414] [Cited by in Crossref: 18] [Cited by in F6Publishing: 15] [Article Influence: 3.6] [Reference Citation Analysis]
Number Citing Articles
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5 Tekendo-Ngongang C, Kruszka P, Martinez AF, Muenke M. Novel heterozygous variants in KMT2D associated with holoprosencephaly. Clin Genet 2019;96:266-70. [PMID: 31282990 DOI: 10.1111/cge.13598] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 2.3] [Reference Citation Analysis]
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8 Berglund A, Stochholm K, Gravholt CH. The epidemiology of sex chromosome abnormalities. Am J Med Genet C Semin Med Genet 2020;184:202-15. [PMID: 32506765 DOI: 10.1002/ajmg.c.31805] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
9 Wang H, Page R, Lopez D, Arkatkar S, Young C, Martinez D, Robbins-Furman P, Montalvo-Liendo N, Chen LS. Pregnant Latinas' views of adopting exome sequencing into newborn screening: A qualitative study. Genet Med 2022:S1098-3600(22)00741-9. [PMID: 35579624 DOI: 10.1016/j.gim.2022.04.012] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
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12 Uçar A, Abacı A, Pirgon Ö, Dündar B, Tütüncüler F, Çatlı G, Anık A, Kılınç Uğurlu A, Büyükgebiz A; (Turner Study Group). A Synopsis of Current Practice in the Diagnosis and Management of Patients with Turner Syndrome in Turkey: A Survey of 18 Pediatric Endocrinology Centers. J Clin Res Pediatr Endocrinol 2018;10:230-8. [PMID: 29699389 DOI: 10.4274/jcrpe.0003] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.8] [Reference Citation Analysis]
13 Swauger S, Backeljauw P, Hornung L, Shafer J, Casnellie L, Gutmark-Little I. Age at and indication for diagnosis of Turner syndrome in the pediatric population. Am J Med Genet A 2021. [PMID: 34390317 DOI: 10.1002/ajmg.a.62459] [Reference Citation Analysis]
14 Kruszka P, Addissie YA, Tekendo-Ngongang C, Jones KL, Savage SK, Gupta N, Sirisena ND, Dissanayake VHW, Paththinige CS, Aravena T, Nampoothiri S, Yesodharan D, Girisha KM, Patil SJ, Jamuar SS, Goh JC, Utari A, Sihombing N, Mishra R, Chitrakar NS, Iriele BC, Lulseged E, Megarbane A, Uwineza A, Oyenusi EE, Olopade OB, Fasanmade OA, Duenas-Roque MM, Thong MK, Tung JYL, Mok GTK, Fleischer N, Rwegerera GM, de Herreros MB, Watts J, Fieggen K, Huckstadt V, Moresco A, Obregon MG, Hussen DF, Ashaat NA, Ashaat EA, Chung BHY, Badoe E, Faradz SMH, El Ruby MO, Shotelersuk V, Wonkam A, Ekure EN, Phadke SR, Richieri-Costa A, Muenke M. Turner syndrome in diverse populations. Am J Med Genet A 2020;182:303-13. [PMID: 31854143 DOI: 10.1002/ajmg.a.61461] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 1.7] [Reference Citation Analysis]
15 Han S, Xu H, Zheng J, Sun J, Feng X, Wang Y, Ye W, Ke Q, Ren Y, Yao S, Zhang S, Chen J, Griggs RC, Zhao Z, Qi M, Gatheridge MA. Population-Wide Duchenne Muscular Dystrophy Carrier Detection by CK and Molecular Testing. Biomed Res Int 2020;2020:8396429. [PMID: 33029525 DOI: 10.1155/2020/8396429] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
16 Purwar N, Tiwari P, Mathur N, Sharma H, Sahlot R, Garg U, Sharma B, Saxena A, Mathur SK. Higher CNV frequencies in Chromsome-14 of girls with Turner syndrome phenotype - A chromosomal microarray study. J Clin Endocrinol Metab 2021:dgab572. [PMID: 34333639 DOI: 10.1210/clinem/dgab572] [Reference Citation Analysis]
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18 Witchel SF, Topaloglu AK. Puberty. Yen and Jaffe's Reproductive Endocrinology. Elsevier; 2019. pp. 394-446.e16. [DOI: 10.1016/b978-0-323-47912-7.00017-2] [Cited by in Crossref: 5] [Article Influence: 1.7] [Reference Citation Analysis]