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  1. Rehman, Atteeq U. [Author]; Najafi, Maryam [Author]; Kambouris, Marios [Author]; Al-Gazali, Lihadh [Author]; Makrythanasis, Periklis [Author]; Rad, Abolfazl [Author]; Maroofian, Reza [Author]; Rajab, Anna [Author]; Stark, Zornitza [Author]; Hunter, Jill V. [Author]; Bakey, Zeineb [Author]; Tokita, Mari J. [Author]; He, Weimin [Author]; Vetrini, Francesco [Author]; Petersen, Andrea [Author]; Santoni, Federico A. [Author]; Hamamy, Hanan [Author]; Wu, Kaman [Author]; Jasmi, Fatma Al [Author]; Helmstädter, Martin [Author]; Arnold, Sebastian Johannes [Author]; Xia, Fan [Author]; Richmond, Christopher [Author]; Liu, Pengfei [Author]; [...]

    Biallelic loss of function variants in PPP1R21 cause a neurodevelopmental syndrome with impaired endocytic function

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    New York, NY [u.a.]: Wiley, 2019

    Published in: Human mutation ; 40, 3 (2019), 267-280

  2. Karami Madani, GholamReza; Rad, Abolfazl; Molavi, Mehdi; Ardalan Khales, Sima; Abbaszadegan, Mohammad Reza; Forghanifard, Mohammad Mahdi

    Predicting the Correlation of EZH2 and Cancer Stem Cell Markers in Esophageal Squamous Cell Carcinoma

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    Springer Science and Business Media LLC, 2018

    Published in: Journal of Gastrointestinal Cancer, 49 (2018) 4, Seite 437-441

  3. Rehman, Atteeq U.; Najafi, Maryam; Kambouris, Marios; Al-Gazali, Lihadh; Makrythanasis, Periklis; Rad, Abolfazl; Maroofian, Reza; Rajab, Anna; Stark, Zornitza; Hunter, Jill V.; Bakey, Zeineb; Tokita, Mari J.; He, Weimin; Vetrini, Francesco; Petersen, Andrea; Santoni, Federico A.; Hamamy, Hanan; Wu, Kaman; Al-Jasmi, Fatma; Helmstädter, Martin; Arnold, Sebastian J.; Xia, Fan; Richmond, Christopher; Liu, Pengfei; [...]

    Cover Image, Volume 40, Issue 3

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    Hindawi Limited, 2019

    Published in: Human Mutation, 40 (2019) 3, Seite i-i

  4. Rehman, Atteeq U.; Najafi, Maryam; Kambouris, Marios; Gazali, Lihadh Al; Makrythanasis, Periklis; Rad, Abolfazl; Maroofian, Reza; Rajab, Anna; Stark, Zornitza; Hunter, Jill V.; Bakey, Zeineb; Tokita, Mari J.; He, Weimin; Vetrini, Francesco; Petersen, Andrea; Santoni, Federico A.; Hamamy, Hanan; Wu, Kaman; Jasmi, Fatma Al; Helmstädter, Martin; Arnold, Sebastian J.; Xia, Fan; Richmond, Christopher; Liu, Pengfei; [...]

    Biallelic loss of function variants in PPP1R21 cause a neurodevelopmental syndrome with impaired endocytic function

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    Hindawi Limited, 2018

    Published in: Human Mutation (2018)