Resultados de procura - Werner, Petra

MESP1 Mutations in Patients with Congenital Heart Defects por Werner, Petra, Latney, Brande, Deardorff, Matthew A., Goldmuntz, Elizabeth

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A Novel Locus For Dilated Cardiomyopathy Maps to Canine Chromosome 8 por Werner, Petra, Raducha, Michael G., Prociuk, Ulana, Sleeper, Meg M., Henthorn, Paula S.

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Familial cutaneous lupus erythematosus (CLE) in the German shorthaired pointer maps to CFA18, a canine orthologue to human CLE por Wang, Ping, Zangerl, Barbara, Werner, Petra, Mauldin, Elizabeth A., Casal, Margret L.

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Epilepsy in Irish Wolfhounds por Casal, Margret L., Munuve, Richard M., Janis, M. Anne, Werner, Petra, Henthorn, Paula S.

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Mutation identification in a canine model of X-linked ectodermal dysplasia por Casal, Margret L., Scheidt, Jennifer L., Rhodes, James L., Henthorn, Paula S., Werner, Petra

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Perception, Attitudes, and Experiences Regarding Mental Health Problems and Web Based Mental Health Information Amongst Young People with and without Migration Background in German... por Seven, Ümran Sema, Stoll, Mendy, Dubbert, Dennis, Kohls, Christian, Werner, Petra, Kalbe, Elke

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Polymorphisms in Canine Platelet Glycoproteins Identify Potential Platelet Antigens por Callan, Mary Beth, Werner, Petra, Mason, Nicola J, Meny, Geralyn M, Raducha, Michael G, Henthorn, Paula S

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Mutations in NTRK3 suggest a novel signaling pathway in human congenital heart disease por Werner, Petra, Paluru, Prasuna, Simpson, Anisha M., Latney, Brande, Iyer, Radhika, Brodeur, Garrett M., Goldmuntz, Elizabeth

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The prevalence of 16p12.1 microdeletion in patients with left-sided cardiac lesions por D’Alessandro, Lisa C.A., Werner, Petra, Xie, Hongbo M., Hakonarson, Hakon, White, Peter S., Goldmuntz, Elizabeth

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Rare Copy Number Variants in Patients with Congenital Conotruncal Heart Defects por Xie, Hongbo M., Werner, Petra, Stambolian, Dwight, Bailey-Wilson, Joan E., Hakonarson, Hakon, White, Peter S., Taylor, Deanne M., Goldmuntz, Elizabeth

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