المؤلفون: Australian Red Cross Society, National Office

URL: http://hdl.handle.net/11343/186679
Series: [2016.0049] "MISSING, WOUNDED AND PRISONER OF WAR ENQUIRY CARDS"

المؤلفون: Australian Red Cross Society, National Office

URL: http://hdl.handle.net/11343/186679
Series: [2016.0049] "MISSING, WOUNDED AND PRISONER OF WAR ENQUIRY CARDS"

المؤلفون: Paul MS, Michener SL, Pan H, Chan H, Pfliger JM, Rosenfeld JA, Lerma VC, Tran A, Longley MA, Lewis RA, Weisz-Hubshman M, Bekheirnia MR, Bekheirnia N, Massingham L, Zech M, Wagner M, Engels H, Cremer K, Mangold E, Peters S, Trautmann J, Perne C, Mester JL, Guillen Sacoto MJ, Person R, McDonnell PP, Cohen SR, Lusk L, Cohen ASA, Le Pichon JB, Pastinen T, Zhou D, Engleman K, Racine C, Faivre L, Moutton S, Denommé-Pichon AS, Koh HY, Poduri A, Bolton J, Knopp C, Julia Suh DS, Maier A, Toosi MB, Karimiani EG, Maroofian R, Schaefer GB, Ramakumaran V, Vasudevan P, Banos-Pinero B, Pagnamenta AT, Prasad C, Osmond M, Schuhmann S, Vasileiou G, Russ-Hall S, Scheffer IE, Carvill GL, Mefford H, Bacino CA, Lee BH, Chao 趙孝端 HT

مؤلفون مشاركون: Undiagnosed Diseases Network

المصدر: American journal of human genetics [Am J Hum Genet] 2024 Jun 06; Vol. 111 (6), pp. 1239. Date of Electronic Publication: 2024 May 08.

نوع المنشور: Published Erratum

بيانات الدورية: Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1537-6605 (Electronic) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: PubMed not MEDLINE; MEDLINE

المؤلفون: Mullegama SV, Kiernan KA, Torti E, Pavlovsky E, Tilton N, Sekula A, Gao H, Alaimo JT, Engleman K, Rush ET, Blocker K, Dipple KM, Fettig VM, Hare H, Glass I, Grange DK, Griffin M, Phornphutkul C, Massingham L, Mehta L, Miller DE, Thies J, Merritt JL 2nd, Muller E 2nd, Osmond M, Sawyer SL, Slaugh R, Hickey RE, Wolf B, Choudhary S, Simonović M, Zhang Y, Palculict TB, Telegrafi A, Carere DA, Wentzensen IM, Morrow MM, Monaghan KG, Juusola J, Yang J

مؤلفون مشاركون: Care4Rare Canada Consortium, Undiagnosed Diseases Network

المصدر: American journal of human genetics [Am J Hum Genet] 2024 Jun 06; Vol. 111 (6), pp. 1240. Date of Electronic Publication: 2024 May 14.

نوع المنشور: Published Erratum

بيانات الدورية: Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1537-6605 (Electronic) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: PubMed not MEDLINE; MEDLINE

المؤلفون: Caylor, R. C.^Aff1, Grote, L.^{Aff2, Aff3}, Thiffault, I.^{Aff1, Aff4, Aff5}, Farrow, E. G.^{Aff4, Aff3, Aff5}, Willig, L.^{Aff4, Aff6, Aff3, Aff5}, Soden, S.^{Aff4, Aff3, Aff5}, Amudhavalli, S. M.^{Aff2, Aff3, Aff5}, Nopper, A. J.^{Aff7, Aff3, Aff5}, Horii, K. A.^{Aff7, Aff3, Aff5}, Fleming, E.^{Aff2, Aff3}, Jenkins, J.^{Aff2, Aff3}, Welsh, H.^{Aff2, Aff3}, Ilyas, M.^{Aff8, Aff3, Aff5}, Engleman, K.^{Aff2, Aff3}, Abdelmoity, A.^{Aff8, Aff3, Aff5}, Saunders, C. J.^{Aff1, Aff4, Aff5}

المصدر: neurogenetics. 19(3):205-213

المؤلفون: Caylor, R. C.^Aff1, Grote, L.^{Aff2, Aff3}, Thiffault, I.^{Aff1, Aff4, Aff5}, Farrow, E. G.^{Aff4, Aff3, Aff5}, Willig, L.^{Aff4, Aff6, Aff3, Aff5}, Soden, S.^{Aff4, Aff3, Aff5}, Amudhavalli, S. M.^{Aff2, Aff3, Aff5}, Nopper, A. J.^{Aff7, Aff3, Aff5}, Horii, K. A.^{Aff7, Aff3, Aff5}, Fleming, E.^{Aff2, Aff3}, Jenkins, J.^{Aff2, Aff3}, Welsh, H.^{Aff2, Aff3}, Ilyas, M.^{Aff8, Aff3, Aff5}, Engleman, K.^{Aff2, Aff3}, Abdelmoity, A.^{Aff8, Aff3, Aff5}, Saunders, C. J.^{Aff1, Aff4, Aff5}

المصدر: neurogenetics. 19(4):261-262

المؤلفون: Coffman K; Division of Neurology, Children's Mercy Hospital, Kansas City, Missouri; University of Missouri Kansas City, School of Medicine, Kansas City, Missouri., Engleman K; Division of Clinical Genetics, Children's Mercy Hospital, Kansas City, Missouri., Shaffer E; Division of Neurology, Children's Mercy Hospital, Kansas City, Missouri., Allison T; Division of Neurology, Children's Mercy Hospital, Kansas City, Missouri; University of Missouri Kansas City, School of Medicine, Kansas City, Missouri., Saunders C; Department of Pathology and Laboratory Medicine, Children's Mercy Hospital, Kansas City, Missouri; Genomic Medicine Center, Children's Mercy Research Institute, Kansas City, Missouri; University of Missouri Kansas City, School of Medicine, Kansas City, Missouri. Electronic address: csaunders@cmh.edu.

المصدر: Pediatric neurology [Pediatr Neurol] 2023 Jul; Vol. 144, pp. 78-79. Date of Electronic Publication: 2023 Apr 07.

نوع المنشور: Letter

بيانات الدورية: Publisher: Elsevier Science Publishing Country of Publication: United States NLM ID: 8508183 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1873-5150 (Electronic) Linking ISSN: 08878994 NLM ISO Abbreviation: Pediatr Neurol Subsets: MEDLINE

مواضيع طبية MeSH: Dystonia*/diagnosis , Dystonia*/genetics , Dystonic Disorders*/diagnosis , Dystonic Disorders*/genetics, Humans ; Phenotype ; Immunoglobulins ; Cell Adhesion Molecules

المؤلفون: Cadieux-Dion M; Department of Pathology and Laboratory Medicine, Children's Mercy Hospital, Kansas City, Missouri, USA., Farrow E; Department of Pediatrics, Children's Mercy Hospital, Kansas City, Missouri, USA.; University of Missouri-Kansas City School of Medicine, Kansas City, Missouri, USA.; Genomic Medicine Center, Children's Mercy Hospital, Kansas City, Missouri, USA., Thiffault I; Department of Pathology and Laboratory Medicine, Children's Mercy Hospital, Kansas City, Missouri, USA.; University of Missouri-Kansas City School of Medicine, Kansas City, Missouri, USA.; Genomic Medicine Center, Children's Mercy Hospital, Kansas City, Missouri, USA., Cohen ASA; Department of Pathology and Laboratory Medicine, Children's Mercy Hospital, Kansas City, Missouri, USA.; University of Missouri-Kansas City School of Medicine, Kansas City, Missouri, USA.; Genomic Medicine Center, Children's Mercy Hospital, Kansas City, Missouri, USA., Welsh H; Department of Pediatrics, Children's Mercy Hospital, Kansas City, Missouri, USA.; University of Missouri-Kansas City School of Medicine, Kansas City, Missouri, USA., Bartik L; Department of Pediatrics, Children's Mercy Hospital, Kansas City, Missouri, USA.; University of Missouri-Kansas City School of Medicine, Kansas City, Missouri, USA., Schwager C; Department of Pediatrics, Children's Mercy Hospital, Kansas City, Missouri, USA.; University of Missouri-Kansas City School of Medicine, Kansas City, Missouri, USA., Engleman K; Department of Pediatrics, Children's Mercy Hospital, Kansas City, Missouri, USA.; University of Missouri-Kansas City School of Medicine, Kansas City, Missouri, USA., Zhou D; Department of Pediatrics, Children's Mercy Hospital, Kansas City, Missouri, USA.; University of Missouri-Kansas City School of Medicine, Kansas City, Missouri, USA., Zhang L; Department of Pathology and Laboratory Medicine, Children's Mercy Hospital, Kansas City, Missouri, USA.; University of Missouri-Kansas City School of Medicine, Kansas City, Missouri, USA., Repnikova E; Department of Pathology and Laboratory Medicine, Children's Mercy Hospital, Kansas City, Missouri, USA.; University of Missouri-Kansas City School of Medicine, Kansas City, Missouri, USA., Amudhavalli SM; Department of Pediatrics, Children's Mercy Hospital, Kansas City, Missouri, USA.; University of Missouri-Kansas City School of Medicine, Kansas City, Missouri, USA., Saunders CJ; Department of Pathology and Laboratory Medicine, Children's Mercy Hospital, Kansas City, Missouri, USA.; University of Missouri-Kansas City School of Medicine, Kansas City, Missouri, USA.; Genomic Medicine Center, Children's Mercy Hospital, Kansas City, Missouri, USA.

المصدر: Clinical genetics [Clin Genet] 2022 Aug; Vol. 102 (2), pp. 136-141. Date of Electronic Publication: 2022 May 18.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Munksgaard Country of Publication: Denmark NLM ID: 0253664 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1399-0004 (Electronic) Linking ISSN: 00099163 NLM ISO Abbreviation: Clin Genet Subsets: MEDLINE

مواضيع طبية MeSH: Autistic Disorder*/genetics , Intellectual Disability*/genetics , Intellectual Disability*/pathology, DNA Copy Number Variations ; Exons ; Humans ; Phenotype ; Polycomb Repressive Complex 2/genetics

المؤلفون: Kummeling, J., Stremmelaar, D.E., Raun, N., Reijnders, M.R., Willemsen, M.H., Ruiterkamp-Versteeg, M., Schepens, M.T.M., Man, C.C.O., Gilissen, C.F.H.A., Cho, M.T., McWalter, K., Sinnema, M., Wheless, J.W., Simon, M.E., Genetti, C.A., Casey, A.M., Terhal, P.A., Smagt, J.J. van der, Gassen, K.L.I. van, Joset, P., Bahr, A., Steindl, K., Rauch, A., Keller, E., Raas-Rothschild, A., Koolen, D.A., Agrawal, P.B., Hoffman, T.L., Powell-Hamilton, N.N., Thiffault, I., Engleman, K., Zhou, D., Bodamer, O., Hoefele, J., Riedhammer, K.M., Schwaibold, E.M.C., Tasic, V., Schubert, D., Top, D., Pfundt, R.P., Higgs, M.R., Kramer, J.M., Kleefstra, T.

المصدر: Molecular Psychiatry; 2013; 2024; 1359-4184; 6; vol. 26; ~Molecular Psychiatry~2013~2024~~~1359-4184~6~26~~

المؤلفون: Martin, J. E., Engleman, K. H.

المصدر: Philosophy, 1990 Oct 01. 65(254), 510-515.

URL الوصول: https://www.jstor.org/stable/3751287