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Results:
1-7
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Results: 7
Authors:
Dollfus, H
Cantenot, L
Rouault, F
Philipp, N
Flament, J
Citation: H. Dollfus et al., Bilateral iridoretinal colobomas in a child with a Noonan phenotype, CLIN DYSMOR, 10(4), 2001, pp. 299-300
Authors:
Dollfus, H
Kumaramanickavel, G
Biswas, P
Stoetzel, C
Quillet, R
Denton, M
Maw, M
Perrin-Schmitt, F
Citation: H. Dollfus et al., Identification of a new TWIST mutation (7p21) with variable eyelid manifestations supports locus homogeneity of BPES at 3q22, J MED GENET, 38(7), 2001, pp. 470-471
Authors:
Porto, FBO
Mack, G
Sterboul, MP
Lewin, P
Flament, J
Sahel, J
Dollfus, H
Citation: Fbo. Porto et al., Isolated late-onset cone-rod dystrophy revealing a familial neurogenic muscle weakness, ataxia, and retinitis pigmentosa syndrome with the T8993G mitochondrial mutation, AM J OPHTH, 132(6), 2001, pp. 935-937
Authors:
Dollfus, H
Hafner, R
Hofmann, HM
Russo, RAG
Denda, L
Gonzales, LD
DeCunto, C
Premoli, J
Melo-Gomez, J
Jorge, JP
Vesely, R
Stubna, M
Dufier, JL
Prieur, AM
Citation: H. Dollfus et al., Chronic infantile neurological cutaneous and articular/neonatal onset multisystem inflammatory disease syndrome - Ocular manifestations in a recentlyrecognized chronic inflammatory disease of childhood, ARCH OPHTH, 118(10), 2000, pp. 1386-1392
Authors:
Goutieres, F
Dollfus, H
Becquet, F
Dufier, JL
Citation: F. Goutieres et al., Extensive brain calcification in two children with bilateral Coats' disease, NEUROPEDIAT, 30(1), 1999, pp. 19-21
Authors:
Alembik, Y
Christmann, D
De Saint Martin, A
Eliot, M
Dollfus, H
Pauly, F
Stoll, C
Citation: Y. Alembik et al., Schinzel-Giedion syndrome with severe deafness and neurodegenerative process, ANN GENET, 42(4), 1999, pp. 225-230
Authors:
Dollfus, H
Dureau, P
Hennequin, C
Uteza, Y
Bron, A
Dufier, JL
Citation: H. Dollfus et al., Congenital toxoplasma chorioretinitis transmitted by preconceptionally immune women, BR J OPHTH, 82(12), 1998, pp. 1444-1445
Risultati:
1-7
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