Arama Sonuçları - "chromosome"

Expanding the application of non-invasive prenatal testing in the detection of foetal chromosomal copy number variations Yazar: Chaohong Wang, Junxiang Tang, Keting Tong, Daoqi Huang, Huayu Tu, Qingnan Li, Jiansheng Zhu

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Complex rearrangements of Y chromosome suggest RPS4Y1 as lymphedema candidate gene Yazar: Po-Fan Chen, Long-Ching Kuan, Chiu-Ching Kao, Hui-Kuo Hsu, Ming Chen, Tsung-Cheng Kuo, Pao-Lin Kuo

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Integrated CNV-seq, karyotyping and SNP-array analyses for effective prenatal diagnosis of chromosomal mosaicism Yazar: Na Ma, Hui Xi, Jing Chen, Ying Peng, Zhengjun Jia, Shuting Yang, Jiancheng Hu, Jialun Pang, Yanan Zhang, Rong Hu, Hua Wang, Jing Liu

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Application of chromosome microarray analysis and karyotyping in diagnostic assessment of abnormal Down syndrome screening results Yazar: Han Kang, Lingxi Wang, Xingyu Li, Chonglan Gao, Yamei Xie, Yu Hu

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Mechanisms Driving Karyotype Evolution and Genomic Architecture

Konular: “…sex chromosomes…”
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DOAB: description of the publication

Cytogenetics Past, Present and Further Perspectives

Konular: “…chromosome, evolution, wheat, hybridization, mammals, karyotype…”
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DOAB: description of the publication

The Bacterial Cell: Coupling between Growth, Nucleoid Replication, Cell Division and Shape Yazar: Arieh Zaritsky

Konular: “…Chromosome replication…”
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DOAB: description of the publication

GENDER PECULIARITIES OF THE SPECTRUM OF CHROMOSOMAL ABERRATIONS IN PERIPHERAL BLOOD LYMPHOCYTES OF HEALTHY PERSONS AND PATIENTS WITH GENERALIZED PERIODONTITIS Yazar: M. I. Khomyk, L. Ye. Kovalchuk, H. M. Melnychuk

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Frequency of chromosomal aneuploidy in high quality embryos from young couples using preimplantation genetic screening Yazar: Farzaneh Fesahat, Fatemeh Montazeri, Mohammad Hasan Sheikhha, Hojjatollah Saeedi, Razieh Dehghani Firouzabadi, Seyed Mehdi Kalantar

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Analysis of positional candidate genes in the AAA1 susceptibility locus for abdominal aortic aneurysms on chromosome 19 Yazar: Ferrell Robert E, Sakalihasan Natzi, Igo Robert P, Lu Qing, Li Ming, Lenk Guy M, Tromp Gerard, Kyo Yoshiki, Lillvis John H, Schworer Charles M, Gatalica Zoran, Land Susan, Kuivaniemi Helena

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Unambiguous molecular detections with multiple genetic approach for the complicated chromosome 22q11 deletion syndrome Yazar: Lin Lung-Huang, Hung Kun-Long, Cheong Mei-Leng, Huang Cheng-Hung, Yang Chen, Yu Yeong-Seng, Chien Chih-Cheng, Huang Huei-Chen, Chen Chan-Wei, Huang Chi-Jung

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Phenotypic variability and management of patients with mosaic monosomy X and Y chromosome material: a case series Yazar: Myriam Ben Fredj, Marwa Messaoud, Sabrine Ben Youssef, Salma Mani, Syrine Laaribi, Rania Sakka, Hayet Ben Hmida, Amine Ksiaa, Mongi Mekki, Mohsen Belghith, Lassaad Sahnoun

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Clinical Correlates of Autosomal Chromosomal Abnormalities in an Electronic Medical Record-Linked Genome-Wide Association Study Yazar: Hayan Jouni M.D, Khader Shameer Ph.D, Yan W. Asmann Ph.D, Ribhi Hazin M.D, Mariza de Andrade Ph.D, Iftikhar J. Kullo M.D

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Genetic polymorphism of 38 Y-chromosome short tandem repeats in Beijing han population from China Yazar: Yan Liu, Chengtao Jiang, Dong Zhao, Jinpei Zhang, Libin Wu, Di Lu, Li Yuan

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Clinical, cytogenetic, and molecular findings in a patient with ring chromosome 4: case report and literature review Yazar: César Paz-, Ana Proaño, Stella D. Verdezoto, Juan Luis García, Jesús María Hernández-Rivas, Paola E. Leone

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A Copy Number Variant on Chromosome 20q13.3 Implicated in Thinness and Severe Obesity Yazar: Sandra J. Hasstedt, Yuanpei Xin, Rong Mao, Tracey Lewis, Ted D. Adams, Steven C. Hunt

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Ophthalmic Treatment and Vision Care of a Patient with Rare Ring Chromosome 15: A Case Report Yazar: Lidia Puchalska-Niedbał, Stanisław Zajączek, Elżbieta Petriczko, Urszula Kulik

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Y-chromosomal Status of Six Indo-European-Speaking Arab Subpopulations in Chaharmahal and Bakhtiari Province, Iran Yazar: Elham BANIMEHDI-DEHKORDI, Behnaz SAFFAR, Mostafa SHAKHSI-NIAEI

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Photosensitivity and Acute Liver Insufficiency in Late-Onset Erythropoietic Protoporphyria with a Chromosome 18q Abnormality Yazar: Yuka Oshikawa, Satoshi Fukushima, Taiga Miyake, Takeshi Kawaguchi, Kenta Motomura, Yasuhiro Nakashima, Kenichi Nakamura, Masatoshi Jinnin, Hironobu Ihn

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YBR/EiJ mice: a new model of glaucoma caused by genes on chromosomes 4 and 17 Yazar: K. Saidas Nair, Mihai Cosma, Narayanan Raghupathy, Michael A. Sellarole, Nicholas G. Tolman, Wilhelmine de Vries, Richard S. Smith, Simon W. M. John

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