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BRCA1 4153delA founder mutation in Russian ovarian cancer patients
Krylova Nadezhda, Lobeiko, Sokolenko, Iyevleva, Rozanov, Mitiushkina, Gergova, Porhanova, Urmancheyeva, Maximov Sergey, Togo, Imyanitov
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BRCA1 4153delA founder mutation in Russian ovarian cancer patients
Krylova Nadezhda, Lobeiko, Sokolenko, Iyevleva, Rozanov, Mitiushkina, Gergova, Porhanova, Urmancheyeva, Maximov Sergey, Togo, Imyanitov
4 pages
English
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Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns
Tanner, Baack, Liyanarachchi Sandya, De, Sturm
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Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns
Tanner, Baack, Liyanarachchi Sandya, De, Sturm
15 pages
English
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Founder mutations and genotype-phenotype correlations in Meckel-Gruber syndrome and associated ciliopathies
Szymanska Katarzyna, Berry Ian, Logan, Cousins, Lindsay Helen, Jafri Hussain, Raashid Yasmin, Malik-Sharif Saghira, Castle Bruce, Ahmed Mushtag, Bennett Chris, Carlton Ruth, Johnson
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Founder mutations and genotype-phenotype correlations in Meckel-Gruber syndrome and associated ciliopathies
Szymanska Katarzyna, Berry Ian, Logan, Cousins, Lindsay Helen, Jafri Hussain, Raashid Yasmin, Malik-Sharif Saghira, Castle Bruce, Ahmed Mushtag, Bennett Chris, Carlton Ruth, Johnson
8 pages
English
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Ancient founder mutation is responsible for Imerslund-Gräsbeck Syndrome among diverse ethnicities
Beech, Liyanarachchi Sandya, Sadiq, Tanner, Shah, Sturm, De
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Ancient founder mutation is responsible for Imerslund-Gräsbeck Syndrome among diverse ethnicities
Beech, Liyanarachchi Sandya, Sadiq, Tanner, Shah, Sturm, De
6 pages
English
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