#founder-mutation

Alternate Text
BRCA1 4153delA founder mutation in Russian ovarian cancer patients
Category

Documents

BRCA1 4153delA founder mutation in Russian ovarian cancer patients

Krylova Nadezhda, Lobeiko, Sokolenko, Iyevleva, Rozanov, Mitiushkina, Gergova, Porhanova, Urmancheyeva, Maximov Sergey, Togo, Imyanitov

BRCA1 4153delA founder mutation in Russian ovarian cancer patients Alternate Text
Category

Documents

Savoirs

BRCA1 4153delA founder mutation in Russian ovarian cancer patients

Krylova Nadezhda, Lobeiko, Sokolenko, Iyevleva, Rozanov, Mitiushkina, Gergova, Porhanova, Urmancheyeva, Maximov Sergey, Togo, Imyanitov

Book

4 pages

Flag

English

icon play Lire
icon play Infos
Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns
Category

Documents

Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns

Tanner, Baack, Liyanarachchi Sandya, De, Sturm

Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns Alternate Text
Category

Documents

Savoirs

Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns

Tanner, Baack, Liyanarachchi Sandya, De, Sturm

Book

15 pages

Flag

English

icon play Lire
icon play Infos
Founder mutations and genotype-phenotype correlations in Meckel-Gruber syndrome and associated ciliopathies
Category

Documents

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

Founder mutations and genotype-phenotype correlations in Meckel-Gruber syndrome and associated ciliopathies Alternate Text
Category

Documents

Savoirs

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

Book

8 pages

Flag

English

icon play Lire
icon play Infos
Ancient founder mutation is responsible for Imerslund-Gräsbeck Syndrome among diverse ethnicities
Category

Documents

Ancient founder mutation is responsible for Imerslund-Gräsbeck Syndrome among diverse ethnicities

Beech, Liyanarachchi Sandya, Sadiq, Tanner, Shah, Sturm, De

Ancient founder mutation is responsible for Imerslund-Gräsbeck Syndrome among diverse ethnicities Alternate Text
Category

Documents

Savoirs

Ancient founder mutation is responsible for Imerslund-Gräsbeck Syndrome among diverse ethnicities

Beech, Liyanarachchi Sandya, Sadiq, Tanner, Shah, Sturm, De

Book

6 pages

Flag

English

icon play Lire
icon play Infos
  • Univers Univers
  • Ebooks Ebooks
  • Livres audio Livres audio
  • Presse Presse
  • Podcasts Podcasts
  • BD BD
  • Documents Documents
Alternate Text