Human Genome Epidemiology Literature Finder
|
Records 1 - 15 (of 15 Records) |
| Query Trace: Disease and PGD[original query] |
|---|
| Novel and known microsatellite markers within the ?-globin cluster to support robust preimplantation genetic diagnosis of ?-thalassemia and sickle cell syndromes. Hemoglobin 2011 1 35 (1): 56-66. Zachaki Sophia, Vrettou Christina, Destouni Aspasia, Kokkali Ggeorgia, Traeger-Synodinos Joanne, Kanavakis Emmanu |
| The single nucleotide polymorphism CRTh2 rs533116 is associated with allergic asthma and increased expression of CRTh2. Allergy 2012 Nov 67 (11): 1357-64. Campos Alberto E, Maclean E, Davidson C, Palikhe N S, Storie J, Tse C, Brenner D, Mayers I, Vliagoftis H, El-Sohemy A, Cameron |
| Variation in PTX3 is associated with primary graft dysfunction after lung transplantation. American journal of respiratory and critical care medicine 2012 Sep 186 (6): 546-52. Diamond Joshua M, Meyer Nuala J, Feng Rui, Rushefski Melanie, Lederer David J, Kawut Steven M, Lee James C, Cantu Edward, Shah Rupal J, Lama Vibha N, Bhorade Sangeeta, Crespo Maria, Demissie Ejigayehu, Sonett Joshua, Wille Keith, Orens Jonathan, Weinacker Ann, Weill David, Arcasoy Selim, Shah Pali D, Belperio John A, Wilkes David, Ware Lorraine B, Palmer Scott M, Christie Jason D, |
| Comparison of whole genome amplification and nested-PCR methods for preimplantation genetic diagnosis for BRCA1 gene mutation on unfertilized oocytes-a pilot study. Hereditary cancer in clinical practice 2013 11 (1): 10. Michalska Danuta, Jaguszewska Kinga, Liss Joanna, Kitowska Kamila, Mirecka Agata, Lukaszuk Krzyszt |
| Hemoglobinopathy carrier prevalence in the United Arab Emirates: first analysis of the Dubai Health Authority premarital screening program results. Hemoglobin 2013 37 (4): 359-68. Belhoul Khawla M, Abdulrahman Mahera, Alraei Rafeeiah |
| CFTR p.Arg117His associated with CBAVD and other CFTR-related disorders. Journal of medical genetics 2013 Feb . Thauvin-Robinet C, Munck A, Huet F, de Becdelièvre A, Jimenez C, Lalau G, Gautier E, Rollet J, Flori J, Nové-Josserand R, Soufir JC, Haloun A, Hubert D, Houssin E, Bellis G, Rault G, David A, Janny L, Chiron R, Rives N, Hairion D, Collignon P, Valeri A, Karsenty G, Rossi A, Audrézet MP, Férec C, Leclerc J, des Georges M, Claustres M, Bienvenu T, Gérard B, Boisseau P, Cabet-Bey F, Cheillan D, Feldmann D, Clavel C, Bieth E, Iron A, Simon-Bouy B, Izard V, Steffann J, Viville S, Costa C, Drouineaud V, Fauque P, Binquet C, Bonithon-Kopp C, Morris MA, Faivre L, Goossens M, Roussey M, Girodon E |
| BRCA mutation carriers show normal ovarian response in in vitro fertilization cycles. Fertility and sterility 2015 Aug . Shapira Moran, Raanani Hila, Feldman Baruch, Srebnik Naama, Dereck-Haim Sanaz, Manela Daphna, Brenghausen Masha, Geva-Lerner Liat, Friedman Eitan, Levi-Lahad Efrat, Goldberg Doron, Perri Tamar, Eldar-Geva Talia, Meirow Dr |
| Multiplex PCR Analysis of 17 (11 Novels) STR Markers Linked to Six Autosomal Recessive Intellectual Disability Genes in Iranian Population. Clinical laboratory 2016 62 (1-2): 31-8. Shirin Ghadami, Maryam Abiri, Farideh Zonozi Rishsefid, Javad Tavakkoly-Bazzaz, Sirous Zeina |
| Genetic study of the PAH locus in the Iranian population: familial gene mutations and minihaplotypes. Metabolic brain disease 2017 Jul . Razipour Masoumeh, Alavinejad Elaheh, Sajedi Seyede Zahra, Talebi Saeed, Entezam Mona, Mohajer Neda, Kazemi-Sefat Golnaz-Ensieh, Gharesouran Jalal, Setoodeh Aria, Mohaddes Ardebili Seyyed Mojtaba, Keramatipour Mohamm |
| [Preimplantation genetic diagnosis for infertile males with autosomal dominant polycystic kidney disease]. Zhonghua nan ke xue = National journal of andrology 2018 9 24 (5): 409-413. Yang Xiao-Yu, Li Tao, Liu Xiao-Jun, Shen Jian-Dong, Cui Yu-Gui, Zhang Gui-Rong, Liu Jia-Y |
| Importance of embryo aneuploidy screening in preimplantation genetic diagnosis for monogenic diseases using the karyomap gene chip. Scientific reports 2018 Feb 8 (1): 3139. Li Gang, Niu Wenbin, Jin Haixia, Xu Jiawei, Song Wenyan, Guo Yihong, Su Yingchun, Sun Ying |
| Preserving fertility in young women undergoing chemotherapy for early breast cancer; the Maastricht experience. Breast cancer research and treatment 2020 4 181 (1): 77-86. Vriens Ingeborg J H, Ter Welle-Butalid Elena M, de Boer Maaike, de Die-Smulders Christine E M, Derhaag Josien G, Geurts Sandra M E, van Hellemond Irene E G, Luiten Ernest J T, Dercksen M Wouter, Lemaire Bea M D, van Haaren Els R M, Vriens Birgit E P J, van de Wouw Agnes J, van Riel Anne-Marie M G H, Janssen-Engelen Sandra L E, van de Poel Marlène H W, Schepers-van der Sterren Ester E M, van Golde Ron J T, Tjan-Heijnen Vivianne C |
| Parental exome analysis identifies shared carrier status for a second recessive disorder in couples with an affected child. European journal of human genetics : EJHG 2020 11 29 (3): 455-462. Mor-Shaked Hagar, Rips Jonathan, Gershon Naamat Shiri, Reich Avichai, Elpeleg Orly, Meiner Vardiella, Harel Tam |
| A systematic review and meta-analysis of toxicity and treatment outcomes with pharmacogenetic-guided dosing compared to standard of care BSA-based fluoropyrimidine dosing. British journal of cancer 2022 3 127 (1): 126-136. Glewis Sarah, Alexander Marliese, Khabib Muhammad N H, Brennan Annabelle, Lazarakis Smaro, Martin Jennifer, Tie Jeanne, Lingaratnam Senthil, Michael Micha |
| Elevated Prostaglandin E Synthesis Is Associated with Clinical and Radiological Disease Severity in Cystic Fibrosis. Journal of clinical medicine 2024 4 13 (7): . Silvia Gartner, Jordi Roca-Ferrer, Paula Fernandez-Alvarez, Isabel Lima, Sandra Rovira-Amigo, Elena García-Arumi, Eduardo F Tizzano, César Pica |
- Page last reviewed:Feb 1, 2024
- Content source: