Deletion of DNA sequences of using a polymerase chain reaction based approach

par Pérez-Pinera,Pablo, Menéndez-González,Manuel, Vega,José Antonio
Publié 2006

Microdeleción del cromosoma Y en paciente infértil oligozoospérmico severo

par Castro G,Andrea, López C,Patricia, Johnson P,M Cecilia, Sovino S,Hugo, Martínez Ch,Claudia, Vantman B,David
Publié 2000

Heterogeneidad de la presentación clínica del síndrome de microdeleción del cromosoma 22, región q11

par Muñoz C,Sebastián, Garay G,Francisco, Flores C,Ingrid, Heusser R,Felipe, Talesnik G,Eduardo, Aracena A,Mariana, Mellado S,Cecilia, Méndez R,Cecilia, Arnaiz G,Pilar, Repetto L,Gabriela
Publié 2001

The upstream sequence of the phycocyanin b subunit gene from Arthrospira platensis regulates expression of gfp gene in response to light intensity

par Yongzhong,Lu, Zhang,Xuecheng
Publié 2005

Germline 3p22.1 microdeletion encompassing RPSA gene is an ultra-rare cause of isolated asplenia

par Aleksandra Oszer, Katarzyna Bąbol-Pokora, Sylwia Kołtan, Agata Pastorczak, Wojciech Młynarski
Publié 2021

Rapid molecular diagnostics of large deletional β0-thalassemia (3.5 kb and 45 kb) using colorimetric LAMP in various thalassemia genotypes

par Wanicha Tepakhan, Wittaya Jomoui
Publié 2021

Case Report: Congenital Brain Dysplasia, Developmental Delay and Intellectual Disability in a Patient With a 7q35-7q36.3 Deletion

par Liang-Liang Fan, Liang-Liang Fan, Liang-Liang Fan, Yue Sheng, Chen-Yu Wang, Ya-Li Li, Ji-Shi Liu, Ji-Shi Liu
Publié 2021

OCP Effects in Catalan Cliticization

par Eulàlia Bonet, Maria-Rosa Lloret
Publié 2002

Imbrication Patterns of Lunda

par Boniface Kawasha
Publié 2021

Fracture Simulation of Structural Glass by Element Deletion in Explicit FEM

par J. Pelfrene, S. van Dam, R. Sevenois, F. Gilabert, W. van Paepegem
Publié 2016

Mechanisms of Congenital Myasthenia Caused by Three Mutations in the COLQ Gene

par Xiaona Luo, Chunmei Wang, Longlong Lin, Fang Yuan, Simei Wang, Yilin Wang, Anqi Wang, Chao Wang, Shengnan Wu, Xiaoping Lan, Quanmei Xu, Rongrong Yin, Hongyi Cheng, Yuanfeng Zhang, Jiaming Xi, Jie Zhang, Xiaomin Sun, Jingbin Yan, Fanyi Zeng, Yucai Chen, Yucai Chen
Publié 2021

Chromosome 9p terminal deletion in nine Egyptian patients and narrowing of the critical region for trigonocephaly

par Amal M. Mohamed, Alaa K. Kamel, Maha M. Eid, Ola M. Eid, Mona Mekkawy, Shymaa H. Hussein, Maha S. Zaki, Samira Esmail, Hanan H. Afifi, Ghada Y. El‐Kamah, Ghada A. Otaify, Heba Ahmed El‐Awady, Aya Elaidy, Mahmoud Y. Essa, Mona El‐Ruby, Engy A. Ashaat, Saida A. Hammad, Inas Mazen, Ghada M. H. Abdel‐Salam, Mona Aglan, Samia Temtamy
Publié 2021

Deleting qseC downregulates virulence and promotes cross-protection in Pasteurella multocida

par Yang Yang, Pei Hu, Lixu Gao, Xiang Yuan, Philip R. Hardwidge, Tian Li, Pan Li, Fang He, Yuanyi Peng, Nengzhang Li
Publié 2021

Tone Sandhi and vowel deletion in Margi

par Bernard Tranel
Publié 1993

Cluster Reduction: Deletion or Coalescence?

par Max W. Wheeler
Publié 2005

How does terminal 21q22 deletion really manifest? Delineation based on prenatal diagnosis and literature review

par Miroslaw Wielgos, Przemyslaw Kosinski, Piotr Jedrzejak, Małgorzata Krajewska-Walasek, Magdalena Bartnik-Glaska, Beata Nowakowska, Aleksandra Jezela-Stanek
Publié 2021

Identification of a Novel VPS13B Mutation in a Chinese Patient with Cohen Syndrome by Whole-Exome Sequencing

par Hu X, Huang T, Liu Y, Zhang L, Zhu L, Peng X, Zhang S
Publié 2021

The Structure of Split Questions in Mandarin Chinese

par Wei Ting-Chi
Publié 2020

22q11.2 Deletion Syndrome as a Human Model for Idiopathic Scoliosis

par Steven de Reuver, Jelle F. Homans, Tom P. C. Schlösser, Michiel L. Houben, Vincent F. X. Deeney, Terrence B. Crowley, Ralf Stücker, Saba Pasha, Moyo C. Kruyt, Donna M. McDonald-McGinn, René M. Castelein
Publié 2021

A systems biology approach to explore the impact of maple tree dormancy release on sap variation and maple syrup quality

par Guillaume Quang N’guyen, Nathalie Martin, Mani Jain, Luc Lagacé, Christian R. Landry, Marie Filteau
Publié 2018