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Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...Cytogenetic and genome research, 2005-01, Vol.111 (2), p.140-146
2005
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Journal of veterinary cardiology, 2002-05, Vol.4 (1), p.17-24
2002
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Yearbook of Paediatric Endocrinology, 2022-09
- L, Akin
- K, Rizzoti
- LC, Gregory
- B, Corredor
- Quesne, Stabej P Le
- H, Williams
- F, Buonocore
- S, Mouilleron
- V, Capra
- SM, McGlacken-Byrne
- GA, Martos-Moreno
- DN, Azmanov
- M, Kendirci
- S, Kurtoglu
- JP, Suntharalingham
- C, Galichet
- S, Gustincich
- V, Tasic
- JC, Achermann
- A, Accogli
- A, Filipovska
- A, Tuilpakov
- M, Maghnie
- Z, Gucev
- ZB, Gonen
- LA, Perez-Jurado
- I, Robinson
- R, Lovell-Badge
- J, Argente
- MT, Dattani
2022
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Gene, 2004-10, Vol.340 (2), p.241-249
2004
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American journal of veterinary research, 2005-03, Vol.66 (3), p.432-436
2005
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Yearbook of Paediatric Endocrinology, 2020-10
2020
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Journal of medical genetics, 2012-01, Vol.49 (1), p.27-36
2012
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American journal of human genetics, 2018-08, Vol.103 (2), p.221-231
- Martin, Carol-Anne
- Sarlós, Kata
- Logan, Clare V.
- Thakur, Roshan Singh
- Parry, David A.
- Bizard, Anna H.
- Leitch, Andrea
- Cleal, Louise
- Ali, Nadia Shaukat
- Al-Owain, Mohammed A.
- Allen, William
- Altmüller, Janine
- Aza-Carmona, Miriam
- Barakat, Bushra A.Y.
- Barraza-García, Jimena
- Begtrup, Amber
- Bogliolo, Massimo
- Cho, Megan T.
- Cruz-Rojo, Jaime
- Dhahrabi, Hassan Ali Mundi
- Elcioglu, Nursel H.
- Gorman, Gráinne S.
- Jobling, Rebekah
- Kesterton, Ian
- Kishita, Yoshihito
- Kohda, Masakazu
- Le Quesne Stabej, Polona
- Malallah, Asam Jassim
- Nürnberg, Peter
- Ohtake, Akira
- Okazaki, Yasushi
- Pujol, Roser
- Ramirez, Maria José
- Revah-Politi, Anya
- Shimura, Masaru
- Stevens, Paul
- Taylor, Robert W.
- Turner, Lesley
- Williams, Hywel
- Wilson, Carolyn
- Yigit, Gökhan
- Zahavich, Laura
- Alkuraya, Fowzan S.
- Surralles, Jordi
- Iglesias, Alejandro
- Murayama, Kei
- Wollnik, Bernd
- Dattani, Mehul
- Heath, Karen E.
- Hickson, Ian D.
- Jackson, Andrew P.
2018
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Pathogenic variants in the human m6A reader YTHDC2 are associated with primary ovarian insufficiency
- McGlacken-Byrne, Sinéad M
- Del Valle, Ignacio
- Quesne Stabej, Polona Le
- Bellutti, Laura
- Garcia-Alonso, Luz
- Ocaka, Louise A
- Ishida, Miho
- Suntharalingham, Jenifer P
- Gagunashvili, Andrey
- Ogunbiyi, Olumide K
- Mistry, Talisa
- Buonocore, Federica
- Crespo, Berta
- Moreno, Nadjeda
- Niola, Paola
- Brooks, Tony
- Brain, Caroline E
- Dattani, Mehul T
- Kelberman, Daniel
- Vento-Tormo, Roser
- Lagos, Carlos F
- Livera, Gabriel
- Conway, Gerard S
- Achermann, John C
2022
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American journal of human genetics, 2024-05, Vol.111 (5), p.996-996
- Martin, Carol-Anne
- Sarlós, Kata
- Logan, Clare V.
- Thakur, Roshan Singh
- Parry, David A.
- Bizard, Anna H.
- Leitch, Andrea
- Cleal, Louise
- Ali, Nadia Shaukat
- Al-Owain, Mohammed A.
- Allen, William
- Altmüller, Janine
- Aza-Carmona, Miriam
- Barakat, Bushra A.Y.
- Barraza-García, Jimena
- Begtrup, Amber
- Bogliolo, Massimo
- Cho, Megan T.
- Cruz-Rojo, Jaime
- Mundi Dhahrabi, Hassan Ali
- Elcioglu, Nursel H.
- GOSgene
- Gorman, Gráinne S.
- Jobling, Rebekah
- Kesterton, Ian
- Kishita, Yoshihito
- Kohda, Masakazu
- Le Quesne Stabej, Polona
- Malallah, Asam Jassim
- Nürnberg, Peter
- Ohtake, Akira
- Okazaki, Yasushi
- Pujol, Roser
- Ramirez, Maria José
- Revah-Politi, Anya
- Shimura, Masaru
- Stevens, Paul
- Taylor, Robert W.
- Turner, Lesley
- Williams, Hywel
- Wilson, Carolyn
- Yigit, Gökhan
- Zahavich, Laura
- Alkuraya, Fowzan S.
- Surralles, Jordi
- Iglesias, Alejandro
- Murayama, Kei
- Wollnik, Bernd
- Dattani, Mehul
- Heath, Karen E.
- Hickson, Ian D.
- Jackson, Andrew P.
2024
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Genetics in medicine, 2022-02, Vol.24 (2), p.384-397
- Akin, Leyla
- Rizzoti, Karine
- Gregory, Louise C.
- Corredor, Beatriz
- Le Quesne Stabej, Polona
- Williams, Hywel
- Buonocore, Federica
- Mouilleron, Stephane
- Capra, Valeria
- McGlacken-Byrne, Sinead M.
- Martos-Moreno, Gabriel Á.
- Azmanov, Dimitar N.
- Kendirci, Mustafa
- Kurtoglu, Selim
- Suntharalingham, Jenifer P.
- Galichet, Christophe
- Gustincich, Stefano
- Tasic, Velibor
- Achermann, John C.
- Accogli, Andrea
- Filipovska, Aleksandra
- Tuilpakov, Anatoly
- Maghnie, Mohamad
- Gucev, Zoran
- Gonen, Zeynep Burcin
- Pérez-Jurado, Luis A.
- Robinson, Iain
- Lovell-Badge, Robin
- Argente, Jesús
- Dattani, Mehul T.
2022
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American journal of human genetics, 2018-09, Vol.103 (3), p.456-456
- Martin, Carol-Anne
- Sarlós, Kata
- Logan, Clare V.
- Thakur, Roshan Singh
- Parry, David A.
- Bizard, Anna H.
- Leitch, Andrea
- Cleal, Louise
- Ali, Nadia Shaukat
- Al-Owain, Mohammed A.
- Allen, William
- Altmüller, Janine
- Aza-Carmona, Miriam
- Barakat, Bushra A.Y.
- Barraza-García, Jimena
- Begtrup, Amber
- Bogliolo, Massimo
- Cho, Megan T.
- Cruz-Rojo, Jaime
- Dhahrabi, Hassan Ali Mundi
- Elcioglu, Nursel H.
- Gorman, Gráinne S.
- Jobling, Rebekah
- Kesterton, Ian
- Kishita, Yoshihito
- Kohda, Masakazu
- Le Quesne Stabej, Polona
- Malallah, Asam Jassim
- Nürnberg, Peter
- Ohtake, Akira
- Okazaki, Yasushi
- Pujol, Roser
- Ramirez, Maria José
- Revah-Politi, Anya
- Shimura, Masaru
- Stevens, Paul
- Taylor, Robert W.
- Turner, Lesley
- Williams, Hywel
- Wilson, Carolyn
- Yigit, Gökhan
- Zahavich, Laura
- Alkuraya, Fowzan S.
- Surralles, Jordi
- Iglesias, Alejandro
- Murayama, Kei
- Wollnik, Bernd
- Dattani, Mehul
- Heath, Karen E.
- Hickson, Ian D.
- Jackson, Andrew P.
2018
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Paediatrics, The Ear, Skull Base, 2018, Vol.2, p.711-719
8, 2018
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- Cardiomyopathy, Dilated - Genetics
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- Mutation
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