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Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6. [electronic resource] by
- Ratbi, Ilham
- Falkenberg, Kim D
- Sommen, Manou
- Al-Sheqaih, Nada
- Guaoua, Soukaina
- Vandeweyer, Geert
- Urquhart, Jill E
- Chandler, Kate E
- Williams, Simon G
- Roberts, Neil A
- El Alloussi, Mustapha
- Black, Graeme C
- Ferdinandusse, Sacha
- Ramdi, Hind
- Heimler, Audrey
- Fryer, Alan
- Lynch, Sally-Ann
- Cooper, Nicola
- Ong, Kai Ren
- Smith, Claire E L
- Inglehearn, Christopher F
- Mighell, Alan J
- Elcock, Claire
- Poulter, James A
- Tischkowitz, Marc
- Davies, Sally J
- Sefiani, Abdelaziz
- Mironov, Aleksandr A
- Newman, William G
- Waterham, Hans R
- Van Camp, Guy
Producer: 20160105
In:
American journal of human genetics vol. 97
Availability: No items available.
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