Search Results - "Homfray T"

Enhancement of phenotyping for fetal investigation using next‐generation sequencing.

Authors: Mone, F. Homfray, T. Kagan, K. O. et al.

Source: Ultrasound in Obstetrics & Gynecology. Oct2023, Vol. 62 Issue 4, p459-461. 3p.

Prenatal presentation of fetal bradycardia and long QT syndrome.

Authors: Chivers, S. Zidere, V. Vigneswaran, T. V. et al.

Source: Ultrasound in Obstetrics & Gynecology. Jul2026, Vol. 68 Issue 1, p107-115. 9p.

Late onset microcephaly: failure of prenatal diagnosis.

Authors: Schwärzler, P. Homfray, T. Bernard, J. -P. et al.

Source: Ultrasound in Obstetrics & Gynecology. Dec2003, Vol. 22 Issue 6, p640-642. 3p. 3 Graphs.

Prenatal ultrasound diagnosis of Leroy I cell disease.

Authors: Lees, C. Homfray, T. Nicolaides, K. H.

Source: Ultrasound in Obstetrics & Gynecology. Sep2001, Vol. 18 Issue 3, p275-276. 2p.

Counseling in fetal medicine: agenesis of the corpus callosum.

Authors: SANTO, S. D'ANTONIO, F. HOMFRAY, T. et al.

Source: Ultrasound in Obstetrics & Gynecology. Nov2012, Vol. 40 Issue 5, p513-521. 9p.

Outcome of antenatally diagnosed talipes equinovarus in an unselected obstetric population.

Authors: Bakalis, S. Sairam, S. Homfray, T. et al.

Source: Ultrasound in Obstetrics & Gynecology. Sep2002, Vol. 20 Issue 3, p226-229. 4p.

Fetal hydrops and the Incremental yield of Next-generation sequencing over standard prenatal Diagnostic testing (FIND) study: prospective cohort study and meta-analysis.

Authors: Mone, F. Eberhardt, R. Y. Hurles, M. E. et al.

Source: Ultrasound in Obstetrics & Gynecology. Oct2021, Vol. 58 Issue 4, p509-518. 10p.

A report on the impact of rapid prenatal exome sequencing on the clinical management of 52 ongoing pregnancies: a retrospective review.

Authors: Dempsey, E Haworth, A Ive, L et al.

Source: BJOG: An International Journal of Obstetrics & Gynaecology. May2021, Vol. 128 Issue 6, p1012-1019. 8p.

Non-immune fetal hydrops: etiology and outcome according to gestational age at diagnosis.

Authors: Sileo, F. G. Kulkarni, A. Branescu, I. et al.

Source: Ultrasound in Obstetrics & Gynecology. Sep2020, Vol. 56 Issue 3, p416-421. 6p.

Session 4 - Pregnancy Outcome.

Authors: Baines, R. Jones, P.R.M. Konje, J.C. et al.

Source: Journal of Obstetrics & Gynaecology. Mar2002 Supplement 1, Vol. 22, p64-70. 7p.

The prenatal diagnosis of Binder syndrome before 24 weeks of gestation: case report.

Authors: Cook, K. Prefumo, F. Presti, F. et al.

Source: Ultrasound in Obstetrics & Gynecology. Nov2000, Vol. 16 Issue 6, p578-581. 4p.

Diagnosis of fetal abnormalities using exome sequencing: translating research into practice.

Authors: Dempsey, E. Pryce, J. Thilaganathan, B. et al.

Source: Ultrasound in Obstetrics & Gynecology. Nov2020, Vol. 56 Issue 5, p779-779. 1p.

OP03.04: Estimation of aneuploidy detection rates based on nuchal translucency and non-invasive prenatal testing ( NIPT): a cohort study.

Authors: Khalil, A. Mahmood, N. Kulkarni, A. et al.

Source: Ultrasound in Obstetrics & Gynecology. Sep2014 Supplement, Vol. 44, p150-151. 1p.

OP28.06: Prenatal diagnosis of nonimmune hydrops fetalis: what do we tell the parents?

Authors: Santo, S. F. Dias, T. D. Mansour, S. et al.

Source: Ultrasound in Obstetrics & Gynecology. Oct2010 Supplement, Vol. 36 Issue S1, p135-135. 1p.

RNU4ATAC-opathy: Clinical, molecular, and transcriptomic insights from a large cohort.

Authors: Matalon DR Duker AL Arriaga TM et al.

Corporate Authors: Matalon DR Duker AL Arriaga TM et al.

Source: Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2026 Jun 19, pp. 102633. Date of Electronic Publication: 2026 Jun 19.

Publication Type: Journal Article

Journal Info: Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1530-0366 (Electronic) Linking ISSN: 10983600 NLM ISO Abbreviation: Genet Med Subsets: MEDLINE

Is There Potential Clinical Utility in Reporting Variants of Uncertain Significance From Prenatal Sequencing?

Authors: Gibbs A Braham R Ramachandran V et al.

Source: Prenatal diagnosis [Prenat Diagn] 2026 Jun 18. Date of Electronic Publication: 2026 Jun 18.

Publication Type: Journal Article

Journal Info: Publisher: Wiley Country of Publication: England NLM ID: 8106540 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1097-0223 (Electronic) Linking ISSN: 01973851 NLM ISO Abbreviation: Prenat Diagn Subsets: MEDLINE

Advances and Challenges in Prenatal Detection and Genetic Diagnosis of Upper Limb Anomalies: Analysis of a South London and Kent Cohort.

Authors: Ruscitti F Giacchino T Koutoulas L et al.

Source: Prenatal diagnosis [Prenat Diagn] 2025 Jan; Vol. 45 (1), pp. 15-26. Date of Electronic Publication: 2024 Dec 13.

Publication Type: Journal Article

Journal Info: Publisher: Wiley Country of Publication: England NLM ID: 8106540 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1097-0223 (Electronic) Linking ISSN: 01973851 NLM ISO Abbreviation: Prenat Diagn Subsets: MEDLINE

Fetal Bradycardia Prompting the Diagnosis and Management of Parental Long QT Syndrome.

Authors: Ananthan K Chivers S Regan W et al.

Source: Circulation. Arrhythmia and electrophysiology [Circ Arrhythm Electrophysiol] 2025 Dec; Vol. 18 (12), pp. e013360. Date of Electronic Publication: 2025 Dec 02.

Publication Type: Journal Article

Journal Info: Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 101474365 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1941-3084 (Electronic) Linking ISSN: 19413084 NLM ISO Abbreviation: Circ Arrhythm Electrophysiol Subsets: MEDLINE

A feasibility study of whole genome germline testing as an adjunct screening tool in a UK general private practice.

Authors: Jones AB Pichert G Side L et al.

Source: Scientific reports [Sci Rep] 2025 Nov 04; Vol. 15 (1), pp. 38526. Date of Electronic Publication: 2025 Nov 04.

Publication Type: Journal Article

Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN: 2045-2322 (Electronic) Linking ISSN: 20452322 NLM ISO Abbreviation: Sci Rep Subsets: MEDLINE

De novo RANBP2 variant in a fetal demise case with cerebral intraparenchymal hemorrhage.

Authors: Meroni A Kalantari S Arossa A et al.

Source: American journal of medical genetics. Part A [Am J Med Genet A] 2023 Jul; Vol. 191 (7), pp. 1973-1977. Date of Electronic Publication: 2023 Apr 27.

Publication Type: Case Reports; Journal Article

Journal Info: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE