Search Results - Karimi-Nejad, Mohammad Hassan

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  1. 1
    A molecular and clinical study of Larsen syndrome caused by mutations in FLNB

    A molecular and clinical study of Larsen syndrome caused by mutations in FLNB by Bicknell, Louise S, Farrington-Rock, Claire, Shafeghati, Yousef, Rump, Patrick, Alanay, Yasemin, Alembik, Yves, Al-Madani, Navid, Firth, Helen, Karimi-Nejad, Mohammad Hassan, Kim, Chong Ae, Leask, Kathryn, Maisenbacher, Melissa, Moran, Ellen, Pappas, John G, Prontera, Paolo, de Ravel, Thomy, Fryns, Jean-Pierre, Sweeney, Elizabeth, Fryer, Alan, Unger, Sheila, Wilson, L C, Lachman, Ralph S, Rimoin, David L, Cohn, Daniel H, Krakow, Deborah, Robertson, Stephen P

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  2. 2
    Genetic Screening of Leber Congenital Amaurosis in a Large Consanguineous Iranian Family

    Genetic Screening of Leber Congenital Amaurosis in a Large Consanguineous Iranian Family by Rezaie, Tayebeh, Karimi-Nejad, Mohammad-Hassan, Meshkat, Mohammad-Reza, Sohbati, Saeed, Karimi-Nejad, Roxana, Najmabadi, Hossein, Sarfarazi, Mansoor

    Published in Ophthalmic genetics
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    Intragenic SNP haplotypes associated with 84dup18 mutation in TNFRSF11A in four FEO pedigrees suggest three independent origins for this mutation

    Intragenic SNP haplotypes associated with 84dup18 mutation in TNFRSF11A in four FEO pedigrees suggest three independent origins for this mutation by Elahi, Elahe, Shafaghati, Yousef, Asadi, Sareh, Absalan, Farnaz, Goodarzi, Hani, Gharaii, Nava, Karimi-Nejad, Mohammad Hassan, Shahram, Farhad, Hughes, Anne E

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    Intragenic SNP haplotypes associated with 84dup18 mutation in TNFRSF11A in four familial expansile osteolysis pedigrees suggest three independent origins for this mutation

    Intragenic SNP haplotypes associated with 84dup18 mutation in TNFRSF11A in four familial expansile osteolysis pedigrees suggest three independent origins for this mutation by ELAHI, Elahe, SHAFAGHATI, Yousef, ASADI, Sareh, ABSALAN, Farnaz, GOODARZI, Hani, GHARAII, Nava, KARIMI-NEJAD, Mohammad Hassan, SHAHRAM, Farhad, HUGHES, Anne E

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