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The utility of exome sequencing for fetal pleural effusions.
Prenat Diagn. 2020 Apr;40(5):590-595. doi: 10.1002/pd.5650. Epub 2020 Feb 17.
Prenat Diagn. 2020.
PMID: 31994743
Free PMC article.
Chromosomal Microarray Analysis Results From Pregnancies With Various Ultrasonographic Anomalies.
Jelin A, Sagaser K, Lawson C, Forster KR, Leppert K, Hertenstein C, Batista D, Blakemore K.
Jelin A, et al. Among authors: forster kr.
Obstet Gynecol. 2019 Apr;133(4):827-828. doi: 10.1097/AOG.0000000000003207.
Obstet Gynecol. 2019.
PMID: 30913182
Free PMC article.
No abstract available.
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Prenatal diagnosis of Desbuquois dysplasia Type 1: Utilization of high-density SNP array to map homozygosity and identify the gene.
Forster KR, Hooper JE, Blakemore KJ, Baschat AA, Hoover-Fong J.
Forster KR, et al.
Am J Med Genet A. 2019 Dec;179(12):2490-2493. doi: 10.1002/ajmg.a.61372. Epub 2019 Oct 6.
Am J Med Genet A. 2019.
PMID: 31587486
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Etiology and management of early pregnancy renal anhydramnios: Is there a place for serial amnioinfusions?
Jelin AC, Sagaser KG, Forster KR, Ibekwe T, Norton ME, Jelin EB.
Jelin AC, et al. Among authors: forster kr.
Prenat Diagn. 2020 Apr;40(5):528-537. doi: 10.1002/pd.5658. Epub 2020 Feb 19.
Prenat Diagn. 2020.
PMID: 32003482
Free PMC article.
Review.
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Molecular testing strategies in the evaluation of fetal skeletal dysplasia.
Jelin AC, Blakemore K, Trebes S, Sagaser K, Forster KR, Russo M, Hoover-Fong J.
Jelin AC, et al. Among authors: forster kr.
J Matern Fetal Neonatal Med. 2022 Jul;35(14):2788-2794. doi: 10.1080/14767058.2020.1802715. Epub 2020 Aug 4.
J Matern Fetal Neonatal Med. 2022.
PMID: 32752906
Free PMC article.
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Not just a carrier: Clinical presentation and management of patients with heterozygous disease-causing alkaline phosphatase (ALPL) variants identified through expanded carrier screening.
Beck NM, Sagaser KG, Lawson CS, Hertenstein C, Jachens A, Forster KR, Miller KA, Jelin AC, Blakemore KJ, Hoover-Fong J.
Beck NM, et al. Among authors: forster kr.
Mol Genet Genomic Med. 2023 Jan;11(1):e2056. doi: 10.1002/mgg3.2056. Epub 2022 Nov 28.
Mol Genet Genomic Med. 2023.
PMID: 36444396
Free PMC article.
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Fetal akinesia deformation sequence syndrome associated with recessive TTN variants.
Alkhunaizi E, Martin N, Jelin AC, Rosner M, Bailey DJ, Steiner LA, Lakhani S, Ji W, Katzman PJ, Forster KR, Jarinova O, Shannon P, Chitayat D; Care4Rare Canada Consortium.
Alkhunaizi E, et al. Among authors: forster kr.
Am J Med Genet A. 2023 Mar;191(3):760-769. doi: 10.1002/ajmg.a.63071. Epub 2022 Dec 10.
Am J Med Genet A. 2023.
PMID: 36495114
Free PMC article.
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Follow Your Nose: Repeat Nasal Bone Evaluation in First-Trimester Screening for Down Syndrome.
Miller KA, Sagaser KG, Hertenstein CB, Blakemore KJ, Forster KR, Lawson CS, Jelin AC.
Miller KA, et al. Among authors: forster kr.
J Ultrasound Med. 2023 Aug;42(8):1709-1716. doi: 10.1002/jum.16190. Epub 2023 Feb 6.
J Ultrasound Med. 2023.
PMID: 36744578
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