Found: 28
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The Double Bubble Sign: Duodenal Atresia and Associated Genetic Etiologies.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Amnioinfusions to Treat Early Onset Anhydramnios Caused by Renal Anomalies: Background and Rationale for the Renal Anhydramnios Fetal Therapy Trial.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Prenatal ABO/RHD Genotyping: A New Paradigm to Allow for Fresh Whole Blood for Cardiopulmonary Bypass in the Immediate Newborn Period.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Recurrent preterm birth risk assessment for two delivery subtypes: A multivariable analysis.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Skeletal Dysplasias: Growing Therapy for Growing Bones.
- Published in:
- Frontiers in Pharmacology, 2017, v. 8, p. 1, doi. 10.3389/fphar.2017.00079
- By:
- Publication type:
- Article
Fetal CHD and perinatal outcomes.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Follow Your Nose: Repeat Nasal Bone Evaluation in First‐Trimester Screening for Down Syndrome.
- Published in:
- Journal of Ultrasound in Medicine, 2023, v. 42, n. 8, p. 1709, doi. 10.1002/jum.16190
- By:
- Publication type:
- Article
Non‐Immune Hydrops Fetalis: Do Placentomegaly and Polyhydramnios Matter?
- Published in:
- Journal of Ultrasound in Medicine, 2018, v. 37, n. 5, p. 1185, doi. 10.1002/jum.14462
- By:
- Publication type:
- Article
The expanded spectrum of human disease associated with GREB1L likely includes complex congenital heart disease.
- Published in:
- Prenatal Diagnosis, 2024, v. 44, n. 3, p. 343, doi. 10.1002/pd.6527
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- Publication type:
- Article
The genetic etiologies of bilateral renal agenesis.
- Published in:
- Prenatal Diagnosis, 2024, v. 44, n. 2, p. 205, doi. 10.1002/pd.6516
- By:
- Publication type:
- Article
The utility of gene sequencing in identifying an underlying genetic disorder in prenatally suspected lower urinary tract obstruction.
- Published in:
- Prenatal Diagnosis, 2024, v. 44, n. 2, p. 196, doi. 10.1002/pd.6425
- By:
- Publication type:
- Article
A systematic review and meta‐analysis of cell‐free DNA testing for detection of fetal sex chromosome aneuploidy.
- Published in:
- Prenatal Diagnosis, 2023, v. 43, n. 2, p. 133, doi. 10.1002/pd.6298
- By:
- Publication type:
- Article
Prenatal phenotype of 47, XXY (Klinefelter syndrome).
- Published in:
- Prenatal Diagnosis, 2023, v. 43, n. 2, p. 207, doi. 10.1002/pd.6071
- By:
- Publication type:
- Article
The utility of pathologic examination and comprehensive phenotyping for accurate diagnosis with perinatal exome sequencing.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 10, p. 1288, doi. 10.1002/pd.6197
- By:
- Publication type:
- Article
Etiology and management of early pregnancy renal anhydramnios: Is there a place for serial amnioinfusions?
- Published in:
- 2020
- By:
- Publication type:
- journal article
The utility of exome sequencing for fetal pleural effusions.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Genetic diagnosis in first or second trimester pregnancy loss using exome sequencing: a systematic review of human essential genes.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2019, v. 36, n. 8, p. 1539, doi. 10.1007/s10815-019-01499-6
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- Publication type:
- Article
Genetics of non‐isolated hemivertebra: A systematic review of fetal, neonatal, and infant cases.
- Published in:
- Clinical Genetics, 2022, v. 102, n. 4, p. 262, doi. 10.1111/cge.14188
- By:
- Publication type:
- Article
Rare exonic CELSR3 variants identified in Bladder Exstrophy Epispadias Complex.
- Published in:
- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1266210
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- Publication type:
- Article
Prenatal Diagnosis of Fetal Aqueductal Stenosis: A Multicenter Prospective Observational Study through the North American Fetal Therapy Network.
- Published in:
- Fetal Diagnosis & Therapy, 2024, v. 51, n. 3, p. 216, doi. 10.1159/000536037
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- Publication type:
- Article
Neonatal Survival After Serial Amnioinfusions for Bilateral Renal Agenesis: The Renal Anhydramnios Fetal Therapy Trial.
- Published in:
- JAMA: Journal of the American Medical Association, 2023, v. 330, n. 21, p. 2096, doi. 10.1001/jama.2023.21153
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- Publication type:
- Article
Perceived Value of Prenatal Ultrasound Screening: A Survey of Pregnant Women.
- Published in:
- Maternal & Child Health Journal, 2023, v. 27, n. 1, p. 101, doi. 10.1007/s10995-022-03515-1
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- Publication type:
- Article
Indeterminate Prenatal Ultrasounds and Maternal Anxiety: A Prospective Cohort Study.
- Published in:
- Maternal & Child Health Journal, 2021, v. 25, n. 5, p. 802, doi. 10.1007/s10995-020-03042-x
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- Publication type:
- Article
Prenatal ultrasound and molecular diagnosis elucidate the prognosis of Pfeiffer syndrome.
- Published in:
- Case Reports in Perinatal Medicine, 2013, v. 2, n. 1/2, p. 51, doi. 10.1515/crpm-2012-0043
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- Publication type:
- Article
De novo variants identified by trio whole exome sequencing of bladder exstrophy epispadias complex.
- Published in:
- American Journal of Medical Genetics. Part A, 2024, v. 194, n. 4, p. 1, doi. 10.1002/ajmg.a.63501
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- Publication type:
- Article
Fetal akinesia deformation sequence syndrome associated with recessive TTN variants.
- Published in:
- American Journal of Medical Genetics. Part A, 2023, v. 191, n. 3, p. 760, doi. 10.1002/ajmg.a.63071
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- Publication type:
- Article
Obstetrical and neonatal outcomes of cardio‐facio‐cutaneous syndrome: Prenatal consequences of Ras/MAPK dysregulation.
- Published in:
- American Journal of Medical Genetics. Part A, 2023, v. 191, n. 2, p. 323, doi. 10.1002/ajmg.a.63020
- By:
- Publication type:
- Article
Not just a carrier: Clinical presentation and management of patients with heterozygous disease‐causing alkaline phosphatase (ALPL) variants identified through expanded carrier screening.
- Published in:
- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 1, p. 1, doi. 10.1002/mgg3.2056
- By:
- Publication type:
- Article