Results
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261.
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262.
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263.
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264.
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265.
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266.
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268.
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269.
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270.
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271.
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Congenital Titinopathy: Comprehensive characterization and pathogenic insights. [electronic resource] by
- Oates, Emily C
- Jones, Kristi J
- Donkervoort, Sandra
- Charlton, Amanda
- Brammah, Susan
- Smith, John E
- Ware, James S
- Yau, Kyle S
- Swanson, Lindsay C
- Whiffin, Nicola
- Peduto, Anthony J
- Bournazos, Adam
- Waddell, Leigh B
- Farrar, Michelle A
- Sampaio, Hugo A
- Teoh, Hooi Ling
- Lamont, Phillipa J
- Mowat, David
- Fitzsimons, Robin B
- Corbett, Alastair J
- Ryan, Monique M
- O'Grady, Gina L
- Sandaradura, Sarah A
- Ghaoui, Roula
- Joshi, Himanshu
- Marshall, Jamie L
- Nolan, Melinda A
- Kaur, Simranpreet
- Punetha, Jaya
- Töpf, Ana
- Harris, Elizabeth
- Bakshi, Madhura
- Genetti, Casie A
- Marttila, Minttu
- Werlauff, Ulla
- Streichenberger, Nathalie
- Pestronk, Alan
- Mazanti, Ingrid
- Pinner, Jason R
- Vuillerot, Carole
- Grosmann, Carla
- Camacho, Ana
- Mohassel, Payam
- Leach, Meganne E
- Foley, A Reghan
- Bharucha-Goebel, Diana
- Collins, James
- Connolly, Anne M
- Gilbreath, Heather R
- Iannaccone, Susan T
- Castro, Diana
- Cummings, Beryl B
- Webster, Richard I
- Lazaro, Leïla
- Vissing, John
- Coppens, Sandra
- Deconinck, Nicolas
- Luk, Ho-Ming
- Thomas, Neil H
- Foulds, Nicola C
- Illingworth, Marjorie A
- Ellard, Sian
- McLean, Catriona A
- Phadke, Rahul
- Ravenscroft, Gianina
- Witting, Nanna
- Hackman, Peter
- Richard, Isabelle
- Cooper, Sandra T
- Kamsteeg, Erik-Jan
- Hoffman, Eric P
- Bushby, Kate
- Straub, Volker
- Udd, Bjarne
- Ferreiro, Ana
- North, Kathryn N
- Clarke, Nigel F
- Lek, Monkol
- Beggs, Alan H
- Bönnemann, Carsten G
- MacArthur, Daniel G
- Granzier, Henk
- Davis, Mark R
- Laing, Nigel G
Producer: 20190812
In:
Annals of neurology vol. 83
Availability: No items available.
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273.
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274.
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275.
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276.
|
Refined localisation of the genes for nebulin and titin on chromosome 2q allows the assignment of nebulin as a candidate gene for autosomal recessive nemaline myopathy. [electronic resource] by
- Pelin, K
- Ridanpää, M
- Donner, K
- Wilton, S
- Krishnarajah, J
- Laing, N
- Kolmerer, B
- Millevoi, S
- Labeit, S
- de la Chapelle, A
- Wallgren-Petterson, C
Producer: 19980121
In:
European journal of human genetics : EJHG vol. 5
Availability: No items available.
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277.
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|
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278.
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279.
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280.
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