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Hyperechogenic fetal bowel: a large French collaborative study of 682 cases. [electronic resource] by
- Simon-Bouy, B
- Satre, V
- Ferec, C
- Malinge, M C
- Girodon, E
- Denamur, E
- Leporrier, N
- Lewin, P
- Forestier, F
- Muller, F
Producer: 20031212
In:
American journal of medical genetics. Part A vol. 121A
Availability: No items available.
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12.
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Molecular analysis of 53 fragile X families with the probe StB12.3. [electronic resource] by
- Puissant, H
- Malinge, M C
- Larget-Piet, A
- Martin, D
- Chauveau, P
- Odent, S
- Plessis, G
- Parent, P
- Lemarec, B
- Larget-Piet, L
Producer: 19950322
In:
American journal of medical genetics vol. 53
Availability: No items available.
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13.
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Simultaneous MFN2 and GDAP1 mutations cause major mitochondrial defects in a patient with CMT. [electronic resource] by
- Cassereau, J
- Casasnovas, C
- Gueguen, N
- Malinge, M-C
- Guillet, V
- Reynier, P
- Bonneau, D
- Amati-Bonneau, P
- Banchs, I
- Volpini, V
- Procaccio, V
- Chevrollier, A
Producer: 20110624
In:
Neurology vol. 76
Availability: No items available.
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14.
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Mitochondrial DNA A3243G mutation involved in familial diabetes, chronic intestinal pseudo-obstruction and recurrent pancreatitis. [electronic resource] by
- Verny, C
- Amati-Bonneau, P
- Letournel, F
- Person, B
- Dib, N
- Malinge, M-C
- Slama, A
- Le Maréchal, C
- Ferec, C
- Procaccio, V
- Reynier, P
- Bonneau, D
Producer: 20090226
In:
Diabetes & metabolism vol. 34
Availability: No items available.
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15.
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OPA3 gene mutations responsible for autosomal dominant optic atrophy and cataract. [electronic resource] by
- Reynier, P
- Amati-Bonneau, P
- Verny, C
- Olichon, A
- Simard, G
- Guichet, A
- Bonnemains, C
- Malecaze, F
- Malinge, M C
- Pelletier, J B
- Calvas, P
- Dollfus, H
- Belenguer, P
- Malthièry, Y
- Lenaers, G
- Bonneau, D
Producer: 20050505
In:
Journal of medical genetics vol. 41
Availability: No items available.
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16.
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Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in France. [electronic resource] by
- Claustres, M
- Guittard, C
- Bozon, D
- Chevalier, F
- Verlingue, C
- Ferec, C
- Girodon, E
- Cazeneuve, C
- Bienvenu, T
- Lalau, G
- Dumur, V
- Feldmann, D
- Bieth, E
- Blayau, M
- Clavel, C
- Creveaux, I
- Malinge, M C
- Monnier, N
- Malzac, P
- Mittre, H
- Chomel, J C
- Bonnefont, J P
- Iron, A
- Chery, M
- Georges, M D
Producer: 20000919
In:
Human mutation vol. 16
Availability: No items available.
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