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Molecular Genetics & Genomic Medicine|September 23, 2020
The genetic basis for the inverse relationship between rheumatoid arthritis and schizophreniaMansour Zamanpoor, Hamid Ghaedi, Mir Davood OmraniMolecular Genetics & Genomic Medicine|September 7, 2020
Multimodal imaging and genetic characteristics of Chinese patients with USH2A-associated nonsyndromic retinitis pigmentosaChong Chen, Qiao Sun, Mingmin Gu, et al.Molecular Genetics & Genomic Medicine|September 7, 2020
Quality of life and pain in patients with thalidomide embryopathy in JapanKoubun Imai, Hanae Sone, Ken Otomo, et al.Molecular Genetics & Genomic Medicine|September 15, 2020
Sjogren-Larsson Syndrome: A case series of five members from an extended family with a novel mutationKamel T Abidi, Naglaa M Kamal, Ayman A Bakkar A, et al.Molecular Genetics & Genomic Medicine|September 28, 2020
A novel missense heterozygous mutation in MAP3K1 gene causes 46, XY disorder of sex development: case report and literature reviewAisha Al Shamsi, Noura Al Hassani, Moustafa Hamchou, et al.Molecular Genetics & Genomic Medicine|September 2, 2020
Novel compound heterozygous mutations of CLDN16 in a patient with familial hypomagnesemia with hypercalciuria and nephrocalcinosisAlejandro García-Castaño, Ana Perdomo-Ramirez, Mònica Vall-Palomar, et al.Molecular Genetics & Genomic Medicine|September 2, 2020
Genome-wide association study of café-au-lait macule number in neurofibromatosis type 1Heejong Sung, Paula L Hyland, Alexander Pemov, et al.Molecular Genetics & Genomic Medicine|September 2, 2020
Correlation between heparanase gene polymorphism and susceptibility to endometrial cancerHanyu Cao, Shuo Yang, Xiuzhang Yu, et al.Molecular Genetics & Genomic Medicine|November 20, 2019
Monoamino oxidase alleles correlate with the presence of essential hypertension among hypogonadic patientsJosé Luis Royo, Daniel Castellano-Castillo, Maximiliano Ruiz-Galdon, et al.Molecular Genetics & Genomic Medicine|November 22, 2019
The SNP rs4846048 of MTHFR enhances the cervical cancer risk through association with miR-522: A preliminary reportXinyue Zhou, Lili Shan, Jing Na, et al.Pageof 253