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Search Results - Erdem, Haktan B
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Expanding the Genotype-Phenotype Correlations and Mutational Spectrum in Inherited Retinal Diseases: Novel and Recurrent Mutations
by
Sahin, Ibrahim
,
Erdem, Haktan B
,
Bahsi, Taha
,
Saat, Hanife
Published in
Curēus (Palo Alto, CA)
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Becker’s myotonia: novel mutations and clinical variability in patients born to consanguineous parents
by
Sahin, Ibrahim
,
Erdem, Haktan B.
,
Tan, Huseyin
,
Tatar, Abdulgani
Published in
Acta neurologica Belgica
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A De Novo Heterozygous Variant (HBB: c.379delG, p.Val127Cysfs32) Associated with a Mild β-Thalassemia Intermedia Phenotype in a Turkish Child
by
Gürlek-Gökçebay, Dilek
,
Akpinar-Tekgunduz, Sibel
,
Erdem, Haktan B.
,
Yarali, Nese
Published in
Hemoglobin
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High prevalence of multilocus pathogenic variation in neurodevelopmental disorders in the Turkish population
by
Mitani, Tadahiro
,
Isikay, Sedat
,
Gezdirici, Alper
,
Gulec, Elif Yilmaz
,
Punetha, Jaya
,
Fatih, Jawid M.
,
Herman, Isabella
,
Akay, Gulsen
,
Du, Haowei
,
Calame, Daniel G.
,
Ayaz, Akif
,
Tos, Tulay
,
Yesil, Gozde
,
Aydin, Hatip
,
Geckinli, Bilgen
,
Elcioglu, Nursel
,
Candan, Sukru
,
Sezer, Ozlem
,
Erdem, Haktan Bagis
,
Gul, Davut
,
Demiral, Emine
,
Elmas, Muhsin
,
Yesilbas, Osman
,
Kilic, Betul
,
Gungor, Serdal
,
Ceylan, Ahmet C.
,
Bozdogan, Sevcan
,
Ozalp, Ozge
,
Cicek, Salih
,
Aslan, Huseyin
,
Yalcintepe, Sinem
,
Topcu, Vehap
,
Bayram, Yavuz
,
Grochowski, Christopher M.
,
Jolly, Angad
,
Dawood, Moez
,
Duan, Ruizhi
,
Jhangiani, Shalini N.
,
Doddapaneni, Harsha
,
Hu, Jianhong
,
Muzny, Donna M.
,
Marafi, Dana
,
Akdemir, Zeynep Coban
,
Karaca, Ender
,
Carvalho, Claudia M.B.
,
Gibbs, Richard A.
,
Posey, Jennifer E.
,
Lupski, James R.
,
Pehlivan, Davut
Published in
American journal of human genetics
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