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348 results

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Page 1
Genetic study of nonsyndromic coronal craniosynostosis.
Lajeunie E, Le Merrer M, Bonaïti-Pellie C, Marchac D, Renier D. Lajeunie E, et al. Among authors: le merrer m. Am J Med Genet. 1995 Feb 13;55(4):500-4. doi: 10.1002/ajmg.1320550422. Am J Med Genet. 1995. PMID: 7762595
A gene for achondroplasia-hypochondroplasia maps to chromosome 4p.
Le Merrer M, Rousseau F, Legeai-Mallet L, Landais JC, Pelet A, Bonaventure J, Sanak M, Weissenbach J, Stoll C, Munnich A, et al. Le Merrer M, et al. Nat Genet. 1994 Mar;6(3):318-21. doi: 10.1038/ng0394-318. Nat Genet. 1994. PMID: 8012398
A gene for hereditary multiple exostoses maps to chromosome 19p.
Le Merrer M, Legeai-Mallet L, Jeannin PM, Horsthemke B, Schinzel A, Plauchu H, Toutain A, Achard F, Munnich A, Maroteaux P. Le Merrer M, et al. Hum Mol Genet. 1994 May;3(5):717-22. doi: 10.1093/hmg/3.5.717. Hum Mol Genet. 1994. PMID: 8081357
Clinical and genetic heterogeneity of hypochondroplasia.
Rousseau F, Bonaventure J, Legeai-Mallet L, Schmidt H, Weissenbach J, Maroteaux P, Munnich A, Le Merrer M. Rousseau F, et al. Among authors: le merrer m. J Med Genet. 1996 Sep;33(9):749-52. doi: 10.1136/jmg.33.9.749. J Med Genet. 1996. PMID: 8880574 Free PMC article.
Genetic study of scaphocephaly.
Lajeunie E, Le Merrer M, Bonaïti-Pellie C, Marchac D, Renier D. Lajeunie E, et al. Among authors: le merrer m. Am J Med Genet. 1996 Mar 29;62(3):282-5. doi: 10.1002/(SICI)1096-8628(19960329)62:3<282::AID-AJMG15>3.0.CO;2-G. Am J Med Genet. 1996. PMID: 8882788
348 results