ISSN: 0197-3851 - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

ISSN 0197-3851

2291. Utility of novel fetal echocardiographic morphometric measures of the aortic arch in the diagnosis of neonatal coarctation of the aorta3. (29th December 2015)

Authors:: Arya, Bhawna; Bhat, Aarti; Vernon, Margaret; Conwell, Jeffrey; Lewin, Mark
Journal:: Prenatal diagnosis
Issue:: Volume 36:Number 2(2016)
Page Start:: 127
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

2292. Validation of a semiconductor next‐generation sequencing‐based protocol for preimplantation genetic diagnosis of reciprocal translocations. (7th September 2015)

Authors:: Bono, S.; Biricik, A.; Spizzichino, L.; Nuccitelli, A.; Minasi, M. G.; Greco, E.; Spinella, F.; Fiorentino, F.; Chitty, Lyn S.; Bianchi, Diana W.
Journal:: Prenatal diagnosis
Issue:: Volume 35:Number 10(2015:Oct.)
Page Start:: 938
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

2293. Validation of automatic scanning of microscope slides in recovering rare cellular events: application for detection of fetal cells in maternal blood. (21st March 2014)

Authors:: Emad, Ahmed; Bouchard, Eric F.; Lamoureux, Josée; Ouellet, Annie; Dutta, Aparajita; Klingbeil, Uli; Drouin, Régen
Journal:: Prenatal diagnosis
Issue:: Volume 34:Number 6(2014:Jun.)
Page Start:: 538
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

2294. Validation of targeted sequencing of single‐nucleotide polymorphisms for non‐invasive prenatal detection of aneuploidy of chromosomes 13, 18, 21, X, and Y. (24th April 2013)

Authors:: Nicolaides, K. H.; Syngelaki, A.; Gil, M.; Atanasova, V.; Markova, D.; Chitty, Lyn S.; Bianchi, Diana W.
Journal:: Prenatal diagnosis
Issue:: Volume 33:Number 6(2013:Jun.)
Page Start:: 575
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

2295. Validation of two‐channel sequencing‐by‐synthesis for noninvasive prenatal testing of fetal whole and partial chromosome aberrations. (15th February 2016)

Authors:: Neveling, Kornelia; Tjwan Thung, Djie; Beulen, Lean; van Rens‐Buijsman, Wendy; Gomes, Ingrid; van den Heuvel, Simone; Mieloo, Hanneke; Derks‐Prinsen, Irma; Kater‐Baats, Ellen; Faas, Brigitte H. W.
Journal:: Prenatal diagnosis
Issue:: Volume 36:Number 3(2016)
Page Start:: 216
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

2296. Variability in antenatal prognostication of fetal diaphragmatic hernia across the North American Fetal Therapy Network (NAFTNet). (8th December 2019)

Authors:: Abbasi, Nimrah; Cortes, Magda Sanz; Ruano, Rodrigo; Johnson, Anthony; Morgan, Tara; Coleman, Beverly; Baschat, Ahmet; Zaretsky, Michael; Lim, Foong Yen; Bulas, Dorothy; Benachi, Alexandra; Ryan, Greg
Journal:: Prenatal diagnosis
Issue:: Volume 40:Number 3(2020)
Page Start:: 342
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

2297. Variability of ffDNA in maternal plasma does not prevent correct classification of trisomy 21 using MeDIP‐qPCR methodology. (28th May 2013)

Authors:: Kyriakou, Skevi; Kypri, Elena; Spyrou, Christiana; Tsaliki, Evdokia; Velissariou, Voula; Papageorgiou, Elisavet A.; Patsalis, Philippos C.
Other Names:: Chitty Lyn S. guestEditor.; Bianchi Diana W. guestEditor.
Journal:: Prenatal diagnosis
Issue:: Volume 33:Number 7(2013:Jul.)
Page Start:: 650
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

2298. Variable prenatal presentation of Pfeiffer syndrome: Suggested aids to prenatal sonographic diagnosis. (28th February 2018)

Authors:: Saliba, Souha; Morel, Baptiste; Gonzales, Marie; Sénat, Marie‐Victoire; Guilbaud, Lucie; Jouannic, Jean‐Marie; Cassart, Marie; Garel, Catherine; Blondiaux, Eléonore
Journal:: Prenatal diagnosis
Issue:: Volume 38:Number 5(2018)
Page Start:: 349
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

2299. Variable presentation between a mother and a fetus with Goltz syndrome. (12th September 2013)

Authors:: Sellars, Elizabeth A.; Wusik, Katie; Weaver, K. Nicole; Hopkin, Robert J.
Journal:: Prenatal diagnosis
Issue:: Volume 33:Number 12(2013:Dec.)
Page Start:: 1211
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

2300. Variants in the 5'‐UTR of APELA gene in women with preeclampsia. (21st February 2019)

Authors:: Yang, Xin; Bian, Yuehong; Wan, Jipeng; Li, Lei; Yang, Ping; Zhao, Shigang; Zhao, Han
Journal:: Prenatal diagnosis
Issue:: Volume 39:Number 4(2019)
Page Start:: 308
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗