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PubPharm (363)
1
Trends in Reporting of Nuchal Translucency Measurements After the Clinical Introduction of Cell-Free DNA Screening
enthalten in:
Obstetrics and gynecology
| 2024
von
Wen, T.
|
Thornburg, L.
|
Norton, M.
| +7
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2
Monogenic conditions and central nervous system anomalies : A prospective study, systematic review and meta-analysis
enthalten in:
Prenatal diagnosis
| 2024
von
Blayney, G.
|
Laffan, E.
|
Jacob, P.
| +23
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3
Prenatal vs postnatal diagnosis of 22q11.2 deletion syndrome : cardiac and noncardiac outcomes through 1 year of age
enthalten in:
American journal of obstetrics and gynecology
| 2024
von
Freud, L.
|
Galloway, S.
|
Crowley, T.
| +59
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4
The Role of cfDNA Biomarkers and Patient Data in the Early Prediction of Preeclampsia : Artificial Intelligence Model
enthalten in:
American journal of obstetrics and gynecology
| 2024
von
Khalil, A.
|
Bellesia, G.
|
Norton, M.
| +19
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5
The utility of gene sequencing in identifying an underlying genetic disorder in prenatally suspected lower urinary tract obstruction
enthalten in:
Prenatal diagnosis
| 2024
von
Brar, B.
|
Blakemore, K.
|
Hertenstein, C.
| +14
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6
Genetic ancestry and diagnostic yield of exome sequencing in a diverse population
enthalten in:
NPJ genomic medicine
| 2024
von
Mavura, Y.
|
Sahin-Hodoglugil, N.
|
Hodoglugil, U.
| +10
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7
Corrigendum to 'Prenatal Exome and Genome Sequencing for Fetal Structural Abnormalities' : [American Journal of Obstetrics and Gynecology 228 (2023) 140-149
enthalten in:
American journal of obstetrics and gynecology
| 2023
von
Vora, N.
|
Norton, M.
ErratumFor: Am J Obstet Gynecol. 2023 Feb;228(2):140-149. - PMID 36027950
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8
Impact of high-risk prenatal screening results for 22q11.2 deletion syndrome on obstetric and neonatal management : Secondary analysis from the SMART study
enthalten in:
Prenatal diagnosis
| 2023
von
Martin, K.
|
Norton, M.
|
MacPherson, C.
| +17
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9
Perinatal Outcomes Associated With Management of Stage 1 Hypertension
enthalten in:
Obstetrics and gynecology
| 2023
von
Bailey, E.
|
Tita, A.
|
Leach, J.
| +42
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10
Author Correction : Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population
enthalten in:
NPJ genomic medicine
| 2023
von
Slavotinek, A.
|
Rego, S.
|
Sahin-Hodoglugil, N.
| +35
ErratumFor: NPJ Genom Med. 2023 May 26;8(1):10. - PMID 37236975
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The journal of maternal-fetal & neonatal medicine
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