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Results 1 - 20 of 687  for All Library Resources

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Refined by: Journal Title: Prenatal Diagnosis remove MEDLINE remove
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1
Prenatal phenotype of a homozygous nonsense MPDZ variant in a fetus with severe congenital hydrocephalus
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Prenatal phenotype of a homozygous nonsense MPDZ variant in a fetus with severe congenital hydrocephalus

Prenatal diagnosis, 2024-05, Vol.44 (5), p.657 [Peer Reviewed Journal]

2024 John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6546 ;PMID: 38498110

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2
Case report of fetus with Lowe syndrome: Expanding the prenatal phenotype
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Case report of fetus with Lowe syndrome: Expanding the prenatal phenotype

Prenatal diagnosis, 2024-05, Vol.44 (5), p.665 [Peer Reviewed Journal]

2024 John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6563 ;PMID: 38554254

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3
Use of cell-free non-invasive prenatal testing in pregnancies affected by placental mosaicism
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Use of cell-free non-invasive prenatal testing in pregnancies affected by placental mosaicism

Prenatal diagnosis, 2024-05, Vol.44 (5), p.562 [Peer Reviewed Journal]

2024 John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6558 ;PMID: 38520498

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4
"The anxiety coming up to every scan-It destroyed me": A qualitative study of the lived experience of cytomegalovirus infection during pregnancy
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"The anxiety coming up to every scan-It destroyed me": A qualitative study of the lived experience of cytomegalovirus infection during pregnancy

Prenatal diagnosis, 2024-05, Vol.44 (5), p.623 [Peer Reviewed Journal]

2024 The Authors. Prenatal Diagnosis published by John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6564 ;PMID: 38578535

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5
Deep-learning computer vision can identify increased nuchal translucency in the first trimester of pregnancy
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Deep-learning computer vision can identify increased nuchal translucency in the first trimester of pregnancy

Prenatal diagnosis, 2024-05, Vol.44 (5), p.535 [Peer Reviewed Journal]

2024 The Authors. Prenatal Diagnosis published by John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6559 ;PMID: 38558081

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6
Postmortem imaging of fetuses at early gestations: A comparison of microfocus computed tomography with postmortem magnetic resonance at 9.4 T and postmortem ultrasound
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Postmortem imaging of fetuses at early gestations: A comparison of microfocus computed tomography with postmortem magnetic resonance at 9.4 T and postmortem ultrasound

Prenatal diagnosis, 2024-05, Vol.44 (5), p.572 [Peer Reviewed Journal]

2024 John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6532 ;PMID: 38367004

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7
Eliminating first trimester combined testing: Consequences for early detection of significant fetal anomalies
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Eliminating first trimester combined testing: Consequences for early detection of significant fetal anomalies

Prenatal diagnosis, 2024-05, Vol.44 (5), p.544 [Peer Reviewed Journal]

2024 The Authors. Prenatal Diagnosis published by John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6552 ;PMID: 38497783

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8
Prenatal detection of mosaicism for a genome wide uniparental disomy cell line in a cohort of patients: Implications and outcomes
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Prenatal detection of mosaicism for a genome wide uniparental disomy cell line in a cohort of patients: Implications and outcomes

Prenatal diagnosis, 2024-05, Vol.44 (5), p.586 [Peer Reviewed Journal]

2024 John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6554 ;PMID: 38558419

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9
Fetus with multiple congenital anomaly syndrome caused by novel variant in ATP1A2
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Fetus with multiple congenital anomaly syndrome caused by novel variant in ATP1A2

Prenatal diagnosis, 2024-05, Vol.44 (5), p.661 [Peer Reviewed Journal]

2024 John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6560 ;PMID: 38549198

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10
Unbalanced X;Y translocations carrying SRY in prenatal settings: Clinical, molecular, and cytogenetic analysis of three cases
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Unbalanced X;Y translocations carrying SRY in prenatal settings: Clinical, molecular, and cytogenetic analysis of three cases

Prenatal diagnosis, 2024-05, Vol.44 (5), p.580 [Peer Reviewed Journal]

2024 John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6520 ;PMID: 38204192

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11
Prenatal diagnosis (or lack thereof) of arthrogryposis multiplex congenita and its impact on the perinatal experience of parents: A retrospective survey
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Prenatal diagnosis (or lack thereof) of arthrogryposis multiplex congenita and its impact on the perinatal experience of parents: A retrospective survey

Prenatal diagnosis, 2024-05, Vol.44 (5), p.614 [Peer Reviewed Journal]

2024 The Authors. Prenatal Diagnosis published by John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6569 ;PMID: 38578615

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12
Length of hysterotomy for fetal spina bifida repair is associated with prematurity risk
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Length of hysterotomy for fetal spina bifida repair is associated with prematurity risk

Prenatal diagnosis, 2024-05, Vol.44 (5), p.644 [Peer Reviewed Journal]

2024 John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6547 ;PMID: 38502037

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13
Isolated fetal umbilical vein varix and the association with intrauterine fetal death and fetal growth restriction: A systematic review, meta-analysis, and nested retrospective cohort study
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Isolated fetal umbilical vein varix and the association with intrauterine fetal death and fetal growth restriction: A systematic review, meta-analysis, and nested retrospective cohort study

Prenatal diagnosis, 2024-05, Vol.44 (5), p.595 [Peer Reviewed Journal]

2024 The Authors. Prenatal Diagnosis published by John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6538 ;PMID: 38502055

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14
Prenatal diagnosis of ROR-2 related Robinow syndrome presenting with fetal ultrasound findings of mesomelia, vertebral, digital and genital abnormalities
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Prenatal diagnosis of ROR-2 related Robinow syndrome presenting with fetal ultrasound findings of mesomelia, vertebral, digital and genital abnormalities

Prenatal diagnosis, 2024-05, Vol.44 (5), p.653 [Peer Reviewed Journal]

2024 John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6543 ;PMID: 38504427

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15
Performance of cell-free DNA testing for common fetal trisomies in triplet pregnancies
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Performance of cell-free DNA testing for common fetal trisomies in triplet pregnancies

Prenatal diagnosis, 2024-05, Vol.44 (5), p.555 [Peer Reviewed Journal]

2024 The Authors. Prenatal Diagnosis published by John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6548 ;PMID: 38448008

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16
Current controversies in prenatal diagnosis: Noninvasive prenatal testing should replace other screening strategies for fetal trisomies 13, 18, 21
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Current controversies in prenatal diagnosis: Noninvasive prenatal testing should replace other screening strategies for fetal trisomies 13, 18, 21

Prenatal diagnosis, 2024-04, Vol.44 (4), p.381 [Peer Reviewed Journal]

2023 John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6477 ;PMID: 38047733

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17
Limited additional value of karyotyping cultured amniotic fluid cell colonies in addition to microarray on uncultured cells for confirmation of abnormal non-invasive prenatal testing results
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Limited additional value of karyotyping cultured amniotic fluid cell colonies in addition to microarray on uncultured cells for confirmation of abnormal non-invasive prenatal testing results

Prenatal diagnosis, 2024-04, Vol.44 (4), p.401 [Peer Reviewed Journal]

2023 The Authors. Prenatal Diagnosis published by John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6499 ;PMID: 38141050

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18
Prenatal diagnosis and postnatal outcome of closed spinal dysraphism
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Prenatal diagnosis and postnatal outcome of closed spinal dysraphism

Prenatal diagnosis, 2024-04, Vol.44 (4), p.499 [Peer Reviewed Journal]

2023 The Authors. Prenatal Diagnosis published by John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6454 ;PMID: 38013494

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19
Current controversy in prenatal diagnosis: The use of cfDNA to screen for monogenic conditions in low risk populations is ready for clinical use
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Current controversy in prenatal diagnosis: The use of cfDNA to screen for monogenic conditions in low risk populations is ready for clinical use

Prenatal diagnosis, 2024-04, Vol.44 (4), p.389 [Peer Reviewed Journal]

2023 The Authors. Prenatal Diagnosis published by John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6469 ;PMID: 37991340

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20
Diagnosis of inborn errors of metabolism through prenatal exome sequencing with targeted analysis for fetal structural anomalies
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Diagnosis of inborn errors of metabolism through prenatal exome sequencing with targeted analysis for fetal structural anomalies

Prenatal diagnosis, 2024-04, Vol.44 (4), p.432 [Peer Reviewed Journal]

2023 John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6476 ;PMID: 38063435

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