Author/Creator: Chitayat, D. - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Chitayat, D.

1. Beals syndrome (congenital contractural arachnodactyly): prenatal ultrasound findings and molecular analysis. (8th September 2014)

Authors:: Inbar‐Feigenberg, M.; Meirowitz, N.; Nanda, D.; Toi, A.; Okun, N.; Chitayat, D.
Journal:: Ultrasound in obstetrics & gynecology
Issue:: Volume 44:Number 4(2014:Oct.)
Page Start:: 486
Record Type:: Journal Article
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2. De novo WNT5A‐associated autosomal dominant Robinow syndrome suggests specificity of genotype and phenotype. (24th May 2014)

Authors:: Roifman, M.; Marcelis, C.L.M.; Paton, T.; Marshall, C.; Silver, R.; Lohr, J.L.; Yntema, H.G.; Venselaar, H.; Kayserili, H.; van Bon, B.; Seaward, G.; FORGE Canada Consortium; Brunner, H.G.; Chitayat, D.
Journal:: Clinical genetics
Issue:: Volume 87:Number 1(2015:Jan.)
Page Start:: 34
Record Type:: Journal Article
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3. Diagnostic utility of microarray testing in pregnancy loss. (1st September 2015)

Authors:: Rosenfeld, J. A.; Tucker, M. E.; Escobar, L. F.; Neill, N. J.; Torchia, B. S.; McDaniel, L. D.; Schultz, R. A.; Chong, K.; Chitayat, D.
Journal:: Ultrasound in obstetrics & gynecology
Issue:: Volume 46:Number 4(2015:Oct.)
Page Start:: 478
Record Type:: Journal Article
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4. Diagnostic Utility of Microarray Testing in Pregnancy Loss. Issue 1 (January 2016)

Authors:: Rosenfeld, J. A.; Tucker, M. E.; Escobar, L. F.; Neill, N. J.; Torchia, B. S.; McDaniel, L. D.; Schultz, R. A.; Chong, K.; Chitayat, D.
Journal:: Obstetrical & gynecological survey
Issue:: Volume 71:Issue 1(2016)
Page Start:
Record Type:: Journal Article
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5. Disability Experiences and Perspectives Regarding Reproductive Decisions, Parenting, and the Utility of Genetic Services: a Qualitative Study. Issue 6 (16th June 2018)

Authors:: Roadhouse, C.; Shuman, C.; Anstey, K.; Sappleton, K.; Chitayat, D.; Ignagni, E.
Journal:: Journal of genetic counseling
Issue:: Volume 27:Issue 6(2018)
Page Start:: 1360
Record Type:: Journal Article
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6. EP09.06: Chromosomal microarray as a first tier test following diagnostic prenatal procedures: the Toronto Mount Sinai Hospital experience. (September 2016)

Authors:: Alayed, N.; Okun, N.; Chitayat, D.; Kolomietz, E.
Journal:: Ultrasound in obstetrics & gynecology
Issue:: Volume 48(2016)Supplement 1
Page Start:: 300
Record Type:: Journal Article
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7. Fetal skeletal dysplasias in a tertiary care center: radiology, pathology, and molecular analysis of 112 cases. (26th July 2014)

Authors:: Barkova, E.; Mohan, U.; Chitayat, D.; Keating, S.; Toi, A.; Frank, J.; Frank, R.; Tomlinson, G.; Glanc, P.
Journal:: Clinical genetics
Issue:: Volume 87:Number 4(2015:Apr.)
Page Start:: 330
Record Type:: Journal Article
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8. Hypotrichosis‐lymphedema‐telangiectasia‐renal defect associated with a truncating mutation in the SOX18 gene. (16th April 2014)

Authors:: Moalem, S.; Brouillard, P.; Kuypers, D.; Legius, E.; Harvey, E.; Taylor, G.; Francois, M.; Vikkula, M.; Chitayat, D.
Journal:: Clinical genetics
Issue:: Volume 87:Number 4(2015:Apr.)
Page Start:: 378
Record Type:: Journal Article
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9. Long‐term postnatal outcome of fetuses with prenatally suspected septo‐optic dysplasia. (1st September 2020)

Authors:: Shinar, S.; Blaser, S.; Chitayat, D.; Selvanathan, T.; Chau, V.; Shannon, P.; Agrawal, S.; Ryan, G.; Pruthi, V.; Miller, S. P.; Krishnan, P.; Van Mieghem, T.
Journal:: Ultrasound in obstetrics & gynecology
Issue:: Volume 56:Number 3(2020)
Page Start:: 371
Record Type:: Journal Article
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10. Loss of the arginine methyltranserase PRMT7 causes syndromic intellectual disability with microcephaly and brachydactyly. Issue 5 (30th November 2016)

Authors:: Kernohan, K.D.; McBride, A.; Xi, Y.; Martin, N.; Schwartzentruber, J.; Dyment, D.A.; Majewski, J.; Blaser, S.; Boycott, K.M.; Chitayat, D.
Journal:: Clinical genetics
Issue:: Volume 91:Issue 5(2017)
Page Start:: 708
Record Type:: Journal Article
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