Lajeunie E - Search Results

1

Lajeunie E, El Ghouzzi V, Le Merrer M, Munnich A, Bonaventure J, Renier D. Lajeunie E, et al. J Med Genet. 1999 Jan;36(1):9-13. J Med Genet. 1999. PMID: 9950359 Free PMC article.

2

Genetic study of nonsyndromic coronal craniosynostosis.

Lajeunie E, Le Merrer M, Bonaïti-Pellie C, Marchac D, Renier D. Lajeunie E, et al. Am J Med Genet. 1995 Feb 13;55(4):500-4. doi: 10.1002/ajmg.1320550422. Am J Med Genet. 1995. PMID: 7762595

3

No evidence of genetic heterogeneity in Crouzon craniofacial dysostosis.

Ma HW, Lajeunie E, Le Merrer M, de Parseval N, Serville F, Weissenbach J, Munnich A, Renier D. Ma HW, et al. Among authors: lajeunie e. Hum Genet. 1995 Dec;96(6):731-5. doi: 10.1007/BF00210308. Hum Genet. 1995. PMID: 8522336

4

Genetic study of scaphocephaly.

Lajeunie E, Le Merrer M, Bonaïti-Pellie C, Marchac D, Renier D. Lajeunie E, et al. 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

5

Syndromal and nonsyndromal primary trigonocephaly: analysis of a series of 237 patients.

Lajeunie E, Le Merrer M, Marchac D, Renier D. Lajeunie E, et al. Am J Med Genet. 1998 Jan 13;75(2):211-5. doi: 10.1002/(sici)1096-8628(19980113)75:2<211::aid-ajmg19>3.0.co;2-s. Am J Med Genet. 1998. PMID: 9450889

6

[Trigonocephaly: isolated, associated and syndromic forms. Genetic study in a series of 278 patients].

Lajeunie E, Le Merrer M, Arnaud E, Marchac D, Renier D. Lajeunie E, et al. Arch Pediatr. 1998 Aug;5(8):873-9. doi: 10.1016/s0929-693x(98)80130-9. Arch Pediatr. 1998. PMID: 9759293 French.

7

Clinical variability in patients with Apert's syndrome.

Lajeunie E, Cameron R, El Ghouzzi V, de Parseval N, Journeau P, Gonzales M, Delezoide AL, Bonaventure J, Le Merrer M, Renier D. Lajeunie E, et al. J Neurosurg. 1999 Mar;90(3):443-7. doi: 10.3171/jns.1999.90.3.0443. J Neurosurg. 1999. PMID: 10067911

8

Mutations within or upstream of the basic helix-loop-helix domain of the TWIST gene are specific to Saethre-Chotzen syndrome.

El Ghouzzi V, Lajeunie E, Le Merrer M, Cormier-Daire V, Renier D, Munnich A, Bonaventure J. El Ghouzzi V, et al. Among authors: lajeunie e. Eur J Hum Genet. 1999 Jan;7(1):27-33. doi: 10.1038/sj.ejhg.5200240. Eur J Hum Genet. 1999. PMID: 10094188

9

Monozygotic twins with Crouzon syndrome: concordance for craniosynostosis and discordance for thumb duplication.

Lajeunie E, Bonaventure J, El Ghouzzi V, Catala M, Renier D. Lajeunie E, et al. Am J Med Genet. 2000 Mar 13;91(2):159-60. Am J Med Genet. 2000. PMID: 10748419 No abstract available.

10

Fibroblast growth factor receptor 3 mutation in nonsyndromic coronal synostosis: clinical spectrum, prevalence, and surgical outcome.

Renier D, El-Ghouzzi V, Bonaventure J, Le Merrer M, Lajeunie E. Renier D, et al. Among authors: lajeunie e. J Neurosurg. 2000 Apr;92(4):631-6. doi: 10.3171/jns.2000.92.4.0631. J Neurosurg. 2000. PMID: 10761652

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