खोज परिणाम - 1月12日~

Des réseaux et des hommes Participation et contribution de la Suisse à l'internationalisation du sport (1912-1972)

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Periventricular nodular heterotopia and bilateral intraventricular xanthogranulomas in 22q11.2 deletion syndrome द्वारा Moogeh Baharnoori, Daniel M. Mandell, Danielle M. Andrade, Eva W.C. Chow, Anne S. Bassett, Tim-Rasmus Kiehl

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Chromosome 22q11.2 deletion: world definition criteria, standards for diagnosis and monitoring द्वारा M.A. Gonchar, O.L. Logvinova, A.I. Strashok, N.V. Konovalova, D.A. Ivakhnenko

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An Endocrinological Perspective on 22q11.2 Deletion Syndrome: A Single-center Experience द्वारा Yasemin Denkboy Öngen, Şebnem Özemri Sağ, Şehime Gülsün Temel, Erdal Eren

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Thrombocytopenia and Postpartum Hemorrhage in a Woman with Chromosome 22q11.2 Deletion Syndrome द्वारा Sarah L. Pachtman, Kathy Deng, Deepak Nanda

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A Case of Bernard-Soulier Syndrome Associated with 22q11.2 Deletion Syndrome द्वारा Oh Cheol Kwon, Su Hyun Yoon, Sung Han Kang, Hyery Kim, Kyung-Nam Koh, Ho Joon Im

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Frequency of 22q11.2 microdeletion in children with congenital heart defects in western poland द्वारा Zeyland Joanna, Krawczynski Maciej R, Skolozdrzy Joanna, Badura-Stronka Magdalena, Moszura Tomasz, Materna-Kiryluk Anna, Glazar Renata, Wisniewska Marzena, Wolnik-Brzozowska Danuta, Wozniak Anna, Bobkowski Waldemar, Slomski Ryszard, Latos-Bielenska Anna, Siwinska Aldona

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Судомний синдром у підлітка як прояв синдрому делеції 22q11.2 द्वारा O.R. Boyarchuk, L.A. Volianska

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22q11.2 Deletion Syndrome: Impact of Genetics in the Treatment of Conotruncal Heart Defects द्वारा Carolina Putotto, Flaminia Pugnaloni, Marta Unolt, Stella Maiolo, Matteo Trezzi, Maria Cristina Digilio, Annapaola Cirillo, Giuseppe Limongelli, Bruno Marino, Giulio Calcagni, Paolo Versacci

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Chromosome 16p11.2 deletions: another piece in the genetic puzzle of childhood obesity द्वारा del Giudice Emanuele, Grandone Anna, Marzuillo Pierluigi, Perrone Laura

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CLINICAL CASE OF CHROMOSOME 22Q11.2 DELETION SYNDROME (DI-GEORGIE SYNDROME) द्वारा Ирина Анатольевна Никитина, Елена Глебовна Цой, Светлана Владимировна Цигельник, Вадим Гельевич Мозес, Светлана Ивановна Елгина, Елена Владимировна Рудаева

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<b>Avaliação da toxicidade subcrônica do extrato bruto seco de <em>Anacardium occidentale</em> Linn em cães</b> - DOI: 10.4025/actascihealthsci.v28i1.1112 द्वारा Arquimedes Fernandes Monteiro de Melo, Miracy Muniz Albuquerque, Maria Almerice Lopes da Silva, Gracielle Carvalho Gomes, Isabely de Souza Vera Cruz, Vanessa Ribeiro Leite, Jane Sheila Higino

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Ten Years' Exile Memoirs of That Interesting Period of the Life of the Baroness De Stael-Holstein, Written by Herself, during the Years 1810, 1811, 1812, and 1813, and Now First Published from the Original Manuscript, by Her Son. द्वारा Staël, Madame de (Anne-Louise-Germaine), 1766-1817; Staël-Holstein, Auguste Louis, baron de, 1790-1827 [Editor]

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PENGARUH DAYA TARIK IKLAN SHOPEE VERSI "12.12 BIRTHDAY SALE 2020" DI MEDIA SOSIAL INSTAGRAM TERHADAP KEPUTUSAN PEMBELIAN MELALUI APLIKASI SHOPEE (Survei Pada Followers Instagram @shopee_id) द्वारा Dimas Puguh Irvananda,

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The Incidence of Associated Anomalies in Children with Congenital Duodenal Obstruction-A Retrospective Cohort Study of 112 Patients द्वारा Adinda G. H. Pijpers, Laurens D. Eeftinck Schattenkerk, Bart Straver, Petra J. G. Zwijnenburg, Chantal J. M. Broers, Ernest L. W. Van Heurn, Ramon R. Gorter, Joep P. M. Derikx

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Ocular Findings in the 16p11.2 Microdeletion Syndrome: A Case Report and Literature Review द्वारा Cybil S. Stingl, Colleen Jackson-Cook, Natario L. Couser

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Halorubrum sp. TBZ112, an Extremely Halophilic Carotenoid- Producing Archaeon Isolated from Urmia Lake द्वारा Masoud Hamidi, Mohammad Saeid Hejazi, Hossein Nazemyieh, Mohammad Amin Hejazi, Davood Naziri

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Speech Sounds Production, Narrative Skills, and Verbal Memory of Children with 22q11.2 Microdeletion द्वारा Marijana Rakonjac, Goran Cuturilo, Natasa Kovacevic-Grujicic, Ivana Simeunovic, Jovana Kostic, Milena Stevanovic, Danijela Drakulic

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Effect of Physiotherapy on Balance and Gross Motor Skills in a Child With 16p11.2 Microdeletion द्वारा Vaida Kerulienė, Margarita Kaleckienė

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Evans syndrome and antibody deficiency: an atypical presentation of chromosome 22q11.2 deletion syndrome द्वारा Gloria Colarusso, Eleonora Gambineri, Elisabetta Lapi, Tommaso Casini, Fabio Tucci, Francesca Lippi, Chiara Azzari

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