Reply
- PMID: 33387405
- DOI: 10.1002/uog.23564
Reply
Erratum in
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Erratum.Ultrasound Obstet Gynecol. 2022 Oct;60(4):591. doi: 10.1002/uog.26067. Ultrasound Obstet Gynecol. 2022. PMID: 36183351 No abstract available.
Comment on
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ISUOG Practice Guidelines (updated): sonographic examination of the fetal central nervous system. Part 1: performance of screening examination and indications for targeted neurosonography.Ultrasound Obstet Gynecol. 2020 Sep;56(3):476-484. doi: 10.1002/uog.22145. Ultrasound Obstet Gynecol. 2020. PMID: 32870591 No abstract available.
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Re: ISUOG Practice Guidelines (updated): sonographic examination of the fetal central nervous system. Part 1: performance of screening examination and indications for targeted neurosonography.Ultrasound Obstet Gynecol. 2021 Jan;57(1):173-174. doi: 10.1002/uog.23559. Ultrasound Obstet Gynecol. 2021. PMID: 33387414 No abstract available.
References
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- Malinger G, Paladini D, Haratz KK, Monteagudo A, Pilu GL, Timor-Tritsch IE. ISUOG Practice Guidelines (updated): sonographic examination of the fetal central nervous system. Part 1: performance of screening examination and indications for targeted neurosonography. Ultrasound Obstet Gynecol 2020; 56: 476-484.
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- Wapner RJ, Martin CL, Levy B, Ballif BC, Eng CM, Zachary JM, Savage M, Platt LD, Saltzman D, Grobman WA, Klugman S, Scholl T, Simpson JL, McCall K, Aggarwal VS, Bunke B, Nahum O, Patel A, Lamb AN, Thom EA, Beaudet AL, Ledbetter DH, Shaffer LG, Jackson L. Chromosomal microarray versus karyotyping for prenatal diagnosis. N Engl J Med 2012; 367: 2175-2184.
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- Levy B, Wapner R. Prenatal diagnosis by chromosomal microarray analysis. Fertil Steril 2018; 109: 201-212.
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- Jang W, Kim Y, Han E, Park J, Chae H, Kwon A, Choi H, Kim J, Son JO, Lee SJ, Hong BY, Jang DH, Han JY, Lee JH, Kim SY, Lee IG, Sung IK, Moon Y, Kim M, Park JH. Chromosomal microarray analysis as a first-tier clinical diagnostic test in patients with developmental delay/intellectual disability, autism spectrum disorders, and multiple congenital anomalies: a prospective multicenter study in Korea. Ann Lab Med 2019; 39: 299-310.
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- Westerfield L, Darilek S, van den Veyver IB. Counseling challenges with variants of uncertain significance and incidental findings in prenatal genetic screening and diagnosis. J Clin Med 2014; 3: 1018-1032.
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