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Year Number of Results
1989 1
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1997 2
1998 1
1999 1
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2010 1
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Page 1
Prenatal diagnosis in France.
Aymé S, Morichon N, Goujard J, Nisand I. Aymé S, et al. Among authors: morichon n. Eur J Hum Genet. 1997;5 Suppl 1:26-31. Eur J Hum Genet. 1997. PMID: 9101175 Review.
Anti-müllerian hormone in early human development.
Josso N, Lamarre I, Picard JY, Berta P, Davies N, Morichon N, Peschanski M, Jeny R. Josso N, et al. Among authors: morichon n. Early Hum Dev. 1993 Jun;33(2):91-9. doi: 10.1016/0378-3782(93)90204-8. Early Hum Dev. 1993. PMID: 8055780
PAX2 mutations in fetal renal hypodysplasia.
Martinovic-Bouriel J, Benachi A, Bonnière M, Brahimi N, Esculpavit C, Morichon N, Vekemans M, Antignac C, Salomon R, Encha-Razavi F, Attié-Bitach T, Gubler MC. Martinovic-Bouriel J, et al. Among authors: morichon n. Am J Med Genet A. 2010 Apr;152A(4):830-5. doi: 10.1002/ajmg.a.33133. Am J Med Genet A. 2010. PMID: 20358591
[Contribution of genetics].
Lyonnet S, Morichon N, Dommergues M, Dumez Y, Briard ML, Vekemans M, Munnich A. Lyonnet S, et al. Among authors: morichon n. Arch Pediatr. 1999;6 Suppl 2:246s-248s. doi: 10.1016/s0929-693x(99)80428-x. Arch Pediatr. 1999. PMID: 10370496 French. No abstract available.
Identification of novel L1CAM mutations using fluorescence-assisted mismatch analysis.
Saugier-Veber P, Martin C, Le Meur N, Lyonnet S, Munnich A, David A, Hénocq A, Héron D, Jonveaux P, Odent S, Manouvrier S, Moncla A, Morichon N, Philip N, Satge D, Tosi M, Frébourg T. Saugier-Veber P, et al. Among authors: morichon n. Hum Mutat. 1998;12(4):259-66. doi: 10.1002/(SICI)1098-1004(1998)12:4<259::AID-HUMU7>3.0.CO;2-A. Hum Mutat. 1998. PMID: 9744477
Prezygotic origin of the isochromosome 12p in Pallister-Killian syndrome.
Cormier-Daire V, Le Merrer M, Gigarel N, Morichon N, Prieur M, Lyonnet S, Vekemans M, Munnich A. Cormier-Daire V, et al. Among authors: morichon n. Am J Med Genet. 1997 Mar 17;69(2):166-8. doi: 10.1002/(sici)1096-8628(19970317)69:2<166::aid-ajmg9>3.0.co;2-n. Am J Med Genet. 1997. PMID: 9056554
11 results