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Molecular Genetics & Genomic Medicine|July 29, 2016
Linkage and related analyses of Barrett's esophagus and its associated adenocarcinomasXiangqing Sun, Robert Elston, Gary W Falk, et al.
Molecular Genetics & Genomic Medicine|May 16, 2020
Loss-of-function mutation in TSGA10 causes acephalic spermatozoa phenotype in humanYuanyuan Ye, Xiaoli Wei, Yanwei Sha, et al.
Molecular Genetics & Genomic Medicine|May 16, 2020
Clinical and genetic analysis of five Chinese patients with urea cycle disordersZhenzhu Zheng, Yiming Lin, Weihua Lin, et al.
Molecular Genetics & Genomic Medicine|May 19, 2020
Children from nuclear families with bad parental relationship could develop tic symptomsPengcheng Zhu, Min Wu, Pinxian Huang, et al.
Molecular Genetics & Genomic Medicine|May 19, 2020
Medulloblastoma, macrocephaly, and a pathogenic germline PTEN variant: Cause or coincidence?Jussi-Pekka Tolonen, Anne Hekkala, Outi Kuismin, et al.
Molecular Genetics & Genomic Medicine|May 21, 2020
Three Novel Variants identified in FBN1 and TGFBR2 in seven Iranian families with suspected Marfan syndromeFatemeh Bitarafan, Ehsan Razmara, Mehrnoosh Khodaeian, et al.
Molecular Genetics & Genomic Medicine|May 9, 2020
Two different genetic etiologies for tuberous sclerosis complex (TSC) in a single familyKate Mowrey, Mary Kay Koenig, Charles A Szabo, et al.
Molecular Genetics & Genomic Medicine|June 2, 2015
Functional consequences of transferrin receptor-2 mutations causing hereditary hemochromatosis type 3Ricky Joshi, Maya Shvartsman, Erica Morán, et al.
Molecular Genetics & Genomic Medicine|June 2, 2015
Copy number variation in the ATP-binding cassette transporter ABCC6 gene and ABCC6 pseudogenes in patients with pseudoxanthoma elasticumMarianne K Kringen, Camilla Stormo, Jens Petter Berg, et al.
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