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Epilepsy In Women Of Childbearing Age [with Reply]

Autor: Firth, H. V., Lindenbaum, R. H., Rubin, Peter C., Saunders, Michael

Publikováno v: BMJ: British Medical Journal, 1989 Oct . 299(6705), 976-977.

Externí odkaz: https://www.jstor.org/stable/29705679

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The diagnostic yield of genetic and metabolic investigations in syndromic and nonsyndromic patients with autism spectrum disorder, global developmental delay, or intellectual disability from a dedicated neurodevelopmental disorders genetics clinic.

Autor: Postma JK; Department of Genetics, CHEO, Ottawa, Ontario, Canada., Harrison MA; Clinical Research Unit, CHEO, Ottawa, Ontario, Canada., Kutcher S; Clinical Research Unit, CHEO, Ottawa, Ontario, Canada., Webster RJ; Clinical Research Unit, CHEO, Ottawa, Ontario, Canada., Cloutier M; Department of Genetics, CHEO, Ottawa, Ontario, Canada., Bourque DK; Division of Metabolics and Newborn Screening, Department of Pediatrics, CHEO, Ottawa, Ontario, Canada., Yu AC; Division of Metabolics and Newborn Screening, Department of Pediatrics, CHEO, Ottawa, Ontario, Canada., Carter MT; Department of Genetics, CHEO, Ottawa, Ontario, Canada.

Publikováno v: American journal of medical genetics. Part A [Am J Med Genet A] 2024 Nov; Vol. 194 (11), pp. e63791. Date of Electronic Publication: 2024 Jun 20.

A Review to Evaluate Synergies Between Genome Sequencing and Current Diagnostics for Innovative Approach to Congenital Anomaly Management in Indonesia.

Autor: Pradipta, Ariel^1,2 ariel.pradipta@gsilab.id, Paramita, Isabela Andhika², Tjhin, Vincentius Vieri², Fauzan, Ihsan², Chen, David Virya²

Publikováno v: Malaysian Journal of Medicine & Health Sciences. 2024 Supplement, Vol. 20, p98-106. 9p.