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Spectrum of temporal bone abnormalities in patients with Waardenburg syndrome and SOX10 mutations. [electronic resource] by
- Elmaleh-Bergès, M
- Baumann, C
- Noël-Pétroff, N
- Sekkal, A
- Couloigner, V
- Devriendt, K
- Wilson, M
- Marlin, S
- Sebag, G
- Pingault, V
Producer: 20131105
In:
AJNR. American journal of neuroradiology vol. 34
Availability: No items available.
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SOX10 mutations mimic isolated hearing loss. [electronic resource] by
- Pingault, V
- Faubert, E
- Baral, V
- Gherbi, S
- Loundon, N
- Couloigner, V
- Denoyelle, F
- Noël-Pétroff, N
- Ducou Le Pointe, H
- Elmaleh-Bergès, M
- Bondurand, N
- Marlin, S
Producer: 20160627
In:
Clinical genetics vol. 88
Availability: No items available.
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Familial CHARGE syndrome because of CHD7 mutation: clinical intra- and interfamilial variability. [electronic resource] by
- Delahaye, A
- Sznajer, Y
- Lyonnet, S
- Elmaleh-Bergès, M
- Delpierre, I
- Audollent, S
- Wiener-Vacher, S
- Mansbach, A-L
- Amiel, J
- Baumann, C
- Bremond-Gignac, D
- Attié-Bitach, T
- Verloes, A
- Sanlaville, D
Producer: 20071105
In:
Clinical genetics vol. 72
Availability: No items available.
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Simplified gyral pattern in severe developmental microcephalies? New insights from allometric modeling for spatial and spectral analysis of gyrification. [electronic resource] by
- Germanaud, D
- Lefèvre, J
- Fischer, C
- Bintner, M
- Curie, A
- des Portes, V
- Eliez, S
- Elmaleh-Bergès, M
- Lamblin, D
- Passemard, S
- Operto, G
- Schaer, M
- Verloes, A
- Toro, R
- Mangin, J F
- Hertz-Pannier, L
Producer: 20150803
In:
NeuroImage vol. 102 Pt 2
Availability: No items available.
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