Search Results - "cytogenetics"

Mutation spectrum, expression profiling, and prognosis evaluation of Fanconi anemia signaling pathway genes for 4259 patients with myelodysplastic syndromes or acute myeloid leukem... by Lixian Chang, Li Zhang, Beibei Zhao, Xuelian Cheng, Yang Wan, Ranran Zhang, Weiping Yuan, Xingjie Gao, Xiaofan Zhu

Connect to this object online.

Recurrent pregnancy loss: TNF-α and IL-10 polymorphisms by Amrit Kaur, Anupam Kaur

Connect to this object online.

Heterozygous Deletion of Chromosome 15q13.3 in a Boy with Developmental Regression, Global Developmental Delay, Hypotonia, and Short Stature by Allison M. Strauss, Anna C. Buhle, David M. Finkler

Connect to this object online.

Subtelomeric study of 132 patients with mental retardation reveals 9 chromosomal anomalies and contributes to the delineation of submicroscopic deletions of 1pter, 2qter, 4pter, 5q... by Tommerup Niels, Baekgaard Peter, Pedersen Vibeke, Ledaal Paal, Friis Birgitte, Hahnemann Johanne, Hjalgrim Helle, Tümer Zeynep, Sogaard Marie, Cingöz Sultan, Duno Morten, Brondum-Nielsen Karen

Connect to this object online.

Molecular Neuropathology in Practice: Clinical Profiling and Integrative Analysis of Molecular Alterations in Glioblastoma by MacLean P. Nasrallah MD, PhD, Zev A. Binder MD, PhD, Derek A. Oldridge MD, PhD, Jianhua Zhao PhD, FACMG, David B. Lieberman MS, CGC, Jacquelyn J. Roth PhD, Christopher D. Watt MD, PhD, Shrey Sukhadia MS, Eva Klinman PhD, Robert D. Daber PhD, Arati Desai MD, Steven Brem MD, Donald M. O'Rourke MD, Jennifer J. D. Morrissette PhD

Connect to this object online.

Rapid diagnosis of trisomy 13 of maternal origin by quantitative fluorescent polymerase chain reaction analysis in a pregnancy with fetal holoprosencephaly, premaxillary agenesis,... by Chih-Ping Chen, Chao-Yun Wu, Schu-Rern Chern, Shin-Wen Chen, Fang-Tzu Wu, Mang-Shang Lee, Wayseen Wang

Connect to this object online.

Pituitary Macroadenoma in a Girl with Male Karyotype: A Rare Case Study by Fatinah Shahab, Tania Tedjo Minuljo, Calvin Layuk Allo, Dody Priambada, Mahayu Dewi Ariani, Sultana Faradz

Connect to this object online.

Luteal phase support for documented failure of placental steroidogenesis: A case report by Bryan Kratz, MD, Amer Rasheed, John P. Holden, MD

Connect to this object online.

Implementation of pharmacogenetics for treatment of patients with acute lymphoblastic leukemia by Violeta Graiqevci-Uka, Emir Behluli, Rifat Hadziselimovic, Thomas Liehr, Gazmend Temaj

Connect to this object online.

Delaying Effects of Prolactin and Growth Hormone on Aging Processes in Bovine Oocytes Matured In Vitro by Galina N. Singina, Ekaterina N. Shedova, Alexander V. Lopukhov, Olga S. Mityashova, Irina Y. Lebedeva

Connect to this object online.

Comparative evaluation of genotoxicity in tobacco users versus nontobacco users by Arun Jacob Thomas, Bindu J Nair, Sajna Oommen, V Syamkumar, Resmi K Raman

Connect to this object online.

Early Physiological, Cytological and Antioxidative Responses of the Edible Halophyte <i>Chenopodium quinoa</i> Exposed to Salt Stress by Aymen Souid, Lorenza Bellani, Eliana Lanfranca Tassi, Karim Ben Hamed, Vincenzo Longo, Lucia Giorgetti

Connect to this object online.

Gold Nanoparticles for BCR-ABL1 Gene Silencing: Improving Tyrosine Kinase Inhibitor Efficacy in Chronic Myeloid Leukemia by Raquel Vinhas, Alexandra R. Fernandes, Pedro V. Baptista

Connect to this object online.

The Exposure and Hazards of Zinc Oxide Nanoparticles: In Vitro and In Vivo Studies by Parisa Saberi-Hasanabadi, Obeid M Malekshah, Hamidreza Mohammadi

Connect to this object online.

Wheat Evolution and Domestication by Feldman, Moshe, Levy, Avraham A.

Link to Metadata

Association of type I choledochal cyst, type III esophageal atresia, evanescent testicle, and clinodactyly: A case report by Pastor Escárcega-Fujigaki, Guillermo Hernandez-, Hayde Velez-Blanco, Lucia Lopez-Mendez, Raul Anza-Escandon, Antonio-Francisco Ga, Monserrat Paz-Ramirez, Maria-Elena S, Maria-

Connect to this object online.

Prenatal diagnosis of familial transmission of 17q12 microduplication associated with no apparent phenotypic abnormality by Chih-Ping Chen, Chung-Hu Fu, Yi-Hui Lin, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Wayseen Wang

Connect to this object online.

Mosaic trisomy 22 at amniocentesis: Prenatal diagnosis and literature review by Chih-Ping Chen, Ming-Chao Huang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Tzu-Yun Chuang, Dai-Dyi Town, Wayseen Wang

Connect to this object online.

Prenatal diagnosis of Down syndrome: A 13-year retrospective study by Ana Vičić, Tomislav Hafner, Ivanka Bekavac Vlatković, Petra Korać, Dubravko Habek, Feodora Stipoljev

Connect to this object online.

Assessment of second-trimester amniocentesis cases: 10-year experience of a tertiary center by Gündüz, Reyhan, Yaman Tunc, Senem, Buğday, Rezan, Oral, Diclehan, Tekeş, Selahaddin, Yalınkaya, Ahmet

Connect to this object online.