Hasil Pencarian - Miho Ishida

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  1. 1
    Analysis of CDKN1C in fetal growth restriction and pregnancy loss [version 1; peer review: 2 approved]

    Analysis of CDKN1C in fetal growth restriction and pregnancy loss [version 1; peer review: 2 approved] oleh Jenifer P. Suntharalingham, Miho Ishida, Federica Buonocore, Ignacio del Valle, Nita Solanky, Charalambos Demetriou, Lesley Regan, Gudrun E. Moore, John C. Achermann

    Diterbitkan 2019-01-01
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  2. 2
    Emerging phenotypes linked to variants in SAMD9 and MIRAGE syndrome

    Emerging phenotypes linked to variants in SAMD9 and MIRAGE syndrome oleh Jenifer P. Suntharalingham, Miho Ishida, Ignacio Del Valle, Susanne E. Stalman, Nita Solanky, Emma Wakeling, Gudrun E. Moore, John C. Achermann, Federica Buonocore

    Diterbitkan 2022-08-01
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  3. 3
    Analysis of genetic variability in Turner syndrome linked to long-term clinical features

    Analysis of genetic variability in Turner syndrome linked to long-term clinical features oleh Jenifer P. Suntharalingham, Miho Ishida, Antoinette Cameron-Pimblett, Sinead M. McGlacken-Byrne, Federica Buonocore, Ignacio del Valle, Gaganjit Kaur Madhan, Tony Brooks, Gerard S. Conway, John C. Achermann

    Diterbitkan 2023-09-01
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  4. 4
    Paternally expressed, imprinted insulin-like growth factor-2 in chorionic villi correlates significantly with birth weight.

    Paternally expressed, imprinted insulin-like growth factor-2 in chorionic villi correlates significantly with birth weight. oleh Charalambos Demetriou, Sayeda Abu-Amero, Anna C Thomas, Miho Ishida, Reena Aggarwal, Lara Al-Olabi, Lydia J Leon, Jaime L Stafford, Argyro Syngelaki, Donald Peebles, Kypros H Nicolaides, Lesley Regan, Philip Stanier, Gudrun E Moore

    Diterbitkan 2014-01-01
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  5. 5
    QSOX2 Deficiency-induced short stature, gastrointestinal dysmotility and immune dysfunction

    QSOX2 Deficiency-induced short stature, gastrointestinal dysmotility and immune dysfunction oleh Avinaash V. Maharaj, Miho Ishida, Anna Rybak, Reem Elfeky, Afiya Andrews, Aakash Joshi, Frances Elmslie, Anni Joensuu, Katri Kantojärvi, Raina Y. Jia, John R. B. Perry, Edel A. O’Toole, Liam J. McGuffin, Vivian Hwa, Helen L. Storr

    Diterbitkan 2024-09-01
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  6. 6
    Mutations in HYAL2, Encoding Hyaluronidase 2, Cause a Syndrome of Orofacial Clefting and Cor Triatriatum Sinister in Humans and Mice.

    Mutations in HYAL2, Encoding Hyaluronidase 2, Cause a Syndrome of Orofacial Clefting and Cor Triatriatum Sinister in Humans and Mice. oleh Martina M A Muggenthaler, Biswajit Chowdhury, S Naimul Hasan, Harold E Cross, Brian Mark, Gaurav V Harlalka, Michael A Patton, Miho Ishida, Elijah R Behr, Sanjay Sharma, Kenneth Zahka, Eissa Faqeih, Brian Blakley, Mike Jackson, Melissa Lees, Vernon Dolinsky, Leroy Cross, Philip Stanier, Claire Salter, Emma L Baple, Fowzan S Alkuraya, Andrew H Crosby, Barbara Triggs-Raine, Barry A Chioza

    Diterbitkan 2017-01-01
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  7. 7
    Pathogenic variants in the human m6A reader YTHDC2 are associated with primary ovarian insufficiency

    Pathogenic variants in the human m6A reader YTHDC2 are associated with primary ovarian insufficiency oleh Sinéad M. McGlacken-Byrne, Ignacio Del Valle, Polona Le Quesne Stabej, Laura Bellutti, Luz Garcia-Alonso, Louise A. Ocaka, Miho Ishida, Jenifer P. Suntharalingham, Andrey Gagunashvili, Olumide K. Ogunbiyi, Talisa Mistry, Federica Buonocore, GOSgene, Berta Crespo, Nadjeda Moreno, Paola Niola, Tony Brooks, Caroline E. Brain, Mehul T. Dattani, Daniel Kelberman, Roser Vento-Tormo, Carlos F. Lagos, Gabriel Livera, Gerard S. Conway, John C. Achermann

    Diterbitkan 2022-03-01
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