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348 results

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Page 1
Segregation analysis in nonsyndromic holoprosencephaly.
Odent S, Le Marec B, Munnich A, Le Merrer M, Bonaïti-Pellié C. Odent S, et al. Among authors: le marec b, le merrer m. Am J Med Genet. 1998 May 1;77(2):139-43. Am J Med Genet. 1998. PMID: 9605287
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
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
Facial anomalies in D-2-hydroxyglutaric aciduria.
Amiel J, de Lonlay P, Francannet C, Picard A, Bruel H, Rabier D, Le Merrer M, Verhoeven N, Jakobs C, Lyonnet S, Munnich A. Amiel J, et al. Among authors: le merrer m. Am J Med Genet. 1999 Sep 10;86(2):124-9. Am J Med Genet. 1999. PMID: 10449646 Review.
348 results