Search Results - Behluli, Emir

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  1. 1
    Case Report: Identification of likely recurrent CEP290 mutation in a child with Joubert syndrome and cerebello-retinal-renal features. [version 2; peer review: 2 approved]

    Case Report: Identification of likely recurrent CEP290 mutation in a child with Joubert syndrome and cerebello-retinal-renal features. [version 2; peer review: 2 approved] by Spahiu, Lidvana, Sayer, John A, Behluli, Emir, Liehr, Thomas, Temaj, Gazmend

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  2. 2
    Suspicions regarding the genetic inheritance of acute lymphoblastic leukemia in patients with down syndrome

    Suspicions regarding the genetic inheritance of acute lymphoblastic leukemia in patients with down syndrome by Behluli, Emir, Nuhii, Nexhibe, Liehr, Thomas, Temaj, Gazmend

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  3. 3
    Joubert syndrome: Molecular basis and treatment

    Joubert syndrome: Molecular basis and treatment by Spahiu, Lidvana, Behluli, Emir, Grajçevci-Uka, Violeta, Liehr, Thomas, Temaj, Gazmend

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  4. 4
    Three Patterns of Inheritance of Quantitative Dermatoglyphic Traits: Kosovo Albanian Twin Study

    Three Patterns of Inheritance of Quantitative Dermatoglyphic Traits: Kosovo Albanian Twin Study by Temaj, Gazmend, Škarić-Jurić, Tatjana, Butković, Ana, Behluli, Emir, Zajc Petranović, Matea, Moder, Angelika

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  5. 5
    Mucopolysaccharidosis III: Molecular basis and treatment

    Mucopolysaccharidosis III: Molecular basis and treatment by Spahiu, Lidvana, Behluli, Emir, Peterlin, Borut, Nefic, Hilada, Hadziselimovic, Rifat, Liehr, Thomas, Temaj, Gazmend

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  6. 6
    Case Report: Identification of likely recurrent CEP290 mutation in a child with Joubert syndrome and cerebello-retinal-renal features. [version 1; peer review: 1 approved, 1 approved with reservations]

    Case Report: Identification of likely recurrent CEP290 mutation in a child with Joubert syndrome and cerebello-retinal-renal features. [version 1; peer review: 1 approved, 1 approv... by Spahiu, Lidvana, A Sayer, John, Behluli, Emir, Liehr, Thomas, Temaj, Gazmend

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  7. 7
    Type II Pleuropulmonary Blastoma in a 4 Month Old Infant with Negative Dicer1 Mutation on Next Generation Sequencing

    Type II Pleuropulmonary Blastoma in a 4 Month Old Infant with Negative Dicer1 Mutation on Next Generation Sequencing by Spahiu, Lidvana, Gafurri, Zana, Uka, Violeta, Salihu, Shpetim, Maqastena, Rufadije, Behluli, Emir

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  8. 8
    Importance of the adrenergic nerve system in the response of gases in the arterial blood following the provoked bronchospasm

    Importance of the adrenergic nerve system in the response of gases in the arterial blood following the provoked bronchospasm by Islami, Hilmi, Veseli, Arta, Behluli, Emir, Morina, Naim

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  9. 9
    Case Report: Identification of likely recurrent CEP290 mutation in a child with Joubert syndrome and cerebello-retinal-renal features

    Case Report: Identification of likely recurrent CEP290 mutation in a child with Joubert syndrome and cerebello-retinal-renal features by Spahiu, Lidvana, Sayer, John A, Behluli, Emir, Liehr, Thomas, Temaj, Gazmend

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