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Clinical and genetic aspects of KBG syndrome. [electronic resource] by
- Low, Karen
- Ashraf, Tazeen
- Canham, Natalie
- Clayton-Smith, Jill
- Deshpande, Charu
- Donaldson, Alan
- Fisher, Richard
- Flinter, Frances
- Foulds, Nicola
- Fryer, Alan
- Gibson, Kate
- Hayes, Ian
- Hills, Alison
- Holder, Susan
- Irving, Melita
- Joss, Shelagh
- Kivuva, Emma
- Lachlan, Kathryn
- Magee, Alex
- McConnell, Vivienne
- McEntagart, Meriel
- Metcalfe, Kay
- Montgomery, Tara
- Newbury-Ecob, Ruth
- Stewart, Fiona
- Turnpenny, Peter
- Vogt, Julie
- Fitzpatrick, David
- Williams, Maggie
- Smithson, Sarah
Producer: 20171019
In:
American journal of medical genetics. Part A vol. 170
Availability: No items available.
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16.
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Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia. [electronic resource] by
- Meyer, Esther
- Carss, Keren J
- Rankin, Julia
- Nichols, John M E
- Grozeva, Detelina
- Joseph, Agnel P
- Mencacci, Niccolo E
- Papandreou, Apostolos
- Ng, Joanne
- Barral, Serena
- Ngoh, Adeline
- Ben-Pazi, Hilla
- Willemsen, Michel A
- Arkadir, David
- Barnicoat, Angela
- Bergman, Hagai
- Bhate, Sanjay
- Boys, Amber
- Darin, Niklas
- Foulds, Nicola
- Gutowski, Nicholas
- Hills, Alison
- Houlden, Henry
- Hurst, Jane A
- Israel, Zvi
- Kaminska, Margaret
- Limousin, Patricia
- Lumsden, Daniel
- McKee, Shane
- Misra, Shibalik
- Mohammed, Shekeeb S
- Nakou, Vasiliki
- Nicolai, Joost
- Nilsson, Magnus
- Pall, Hardev
- Peall, Kathryn J
- Peters, Gregory B
- Prabhakar, Prab
- Reuter, Miriam S
- Rump, Patrick
- Segel, Reeval
- Sinnema, Margje
- Smith, Martin
- Turnpenny, Peter
- White, Susan M
- Wieczorek, Dagmar
- Wiethoff, Sarah
- Wilson, Brian T
- Winter, Gidon
- Wragg, Christopher
- Pope, Simon
- Heales, Simon J H
- Morrogh, Deborah
- Pittman, Alan
- Carr, Lucinda J
- Perez-Dueñas, Belen
- Lin, Jean-Pierre
- Reis, Andre
- Gahl, William A
- Toro, Camilo
- Bhatia, Kailash P
- Wood, Nicholas W
- Kamsteeg, Erik-Jan
- Chong, Wui K
- Gissen, Paul
- Topf, Maya
- Dale, Russell C
- Chubb, Jonathan R
- Raymond, F Lucy
- Kurian, Manju A
Producer: 20170905
In:
Nature genetics vol. 49
Availability: No items available.
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17.
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Corrigendum: Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia. [electronic resource] by
- Meyer, Esther
- Carss, Keren J
- Rankin, Julia
- Nichols, John M E
- Grozeva, Detelina
- Joseph, Agnel P
- Mencacci, Niccolo E
- Papandreou, Apostolos
- Ng, Joanne
- Barral, Serena
- Ngoh, Adeline
- Ben-Pazi, Hilla
- Willemsen, Michel A
- Arkadir, David
- Barnicoat, Angela
- Bergman, Hagai
- Bhate, Sanjay
- Boys, Amber
- Darin, Niklas
- Foulds, Nicola
- Gutowski, Nicholas
- Hills, Alison
- Houlden, Henry
- Hurst, Jane A
- Israel, Zvi
- Kaminska, Margaret
- Limousin, Patricia
- Lumsden, Daniel
- McKee, Shane
- Misra, Shibalik
- Mohammed, Shekeeb S
- Nakou, Vasiliki
- Nicolai, Joost
- Nilsson, Magnus
- Pall, Hardev
- Peall, Kathryn J
- Peters, Gregory B
- Prabhakar, Prab
- Reuter, Miriam S
- Rump, Patrick
- Segel, Reeval
- Sinnema, Margje
- Smith, Martin
- Turnpenny, Peter
- White, Susan M
- Wieczorek, Dagmar
- Wiethoff, Sarah
- Wilson, Brian T
- Winter, Gidon
- Wragg, Christopher
- Pope, Simon
- Heales, Simon J H
- Morrogh, Deborah
- Pittman, Alan
- Carr, Lucinda J
- Perez-Dueñas, Belen
- Lin, Jean-Pierre
- Reis, Andre
- Gahl, William A
- Toro, Camilo
- Bhatia, Kailash P
- Wood, Nicholas W
- Kamsteeg, Erik-Jan
- Chong, Wui K
- Gissen, Paul
- Topf, Maya
- Dale, Russell C
- Chubb, Jonathan R
- Raymond, F Lucy
- Kurian, Manju A
Publication details: Nature genetics 05 2017
In:
Nature genetics vol. 49
Availability: No items available.
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