Le Merrer M - Search Results

1

Recessive metaphyseal dysplasia without hypotrichosis. A syndrome clinically distinct from McKusick cartilage-hair hypoplasia.

Verloes A, Pierard GE, Le Merrer M, Maroteaux P. Verloes A, et al. Among authors: le merrer m. J Med Genet. 1990 Nov;27(11):693-6. doi: 10.1136/jmg.27.11.693. J Med Genet. 1990. PMID: 2277385 Free PMC article.

2

Metaphyseal acroscyphodysplasia.

Verloes A, Le Merrer M, Farriaux JP, Maroteaux P. Verloes A, et al. Among authors: le merrer m. Clin Genet. 1991 May;39(5):362-9. doi: 10.1111/j.1399-0004.1991.tb03043.x. Clin Genet. 1991. PMID: 1860252

3

Holoprosencephaly-polydactyly ('pseudotrisomy 13') syndrome: a syndrome with features of hydrolethalus and Smith-Lemli-Opitz syndromes. A collaborative multicentre study.

Verloes A, Aymé S, Gambarelli D, Gonzales M, Le Merrer M, Mulliez N, Philip N, Roume J. Verloes A, et al. Among authors: le merrer m. J Med Genet. 1991 May;28(5):297-303. doi: 10.1136/jmg.28.5.297. J Med Genet. 1991. PMID: 1865466 Free PMC article. Review.

4

Osteocraniostenosis.

Verloes A, Narcy F, Grattagliano B, Delezoide AL, Guibaud P, Schaaps JP, Le Merrer M, Maroteaux P. Verloes A, et al. Among authors: le merrer m. J Med Genet. 1994 Oct;31(10):772-8. doi: 10.1136/jmg.31.10.772. J Med Genet. 1994. PMID: 7837254 Free PMC article.

5

Re-evaluation of kyphomelic dysplasia.

Le Merrer M, Cormier Daire V, Maroteaux P. Le Merrer M, et al. Am J Med Genet A. 2003 Jul 15;120A(2):289-91. doi: 10.1002/ajmg.a.20035. Am J Med Genet A. 2003. PMID: 12833417 No abstract available.

6

Metaphyseal chondrodysplasia with cone-shaped epiphyses: a specific form involving the lower limbs.

Dieux-Coëslier A, Moerman A, Holder M, Boute O, Maroteaux P, Manouvrier S, Le Merrer M. Dieux-Coëslier A, et al. Among authors: le merrer m. Am J Med Genet A. 2004 Jan 1;124A(1):60-6. doi: 10.1002/ajmg.a.20411. Am J Med Genet A. 2004. PMID: 14679588

7

Cerebro-osseous-digital syndrome: four new cases of a lethal skeletal dysplasia--distinct from Neu-Laxova Syndrome.

Elliott AM, Gonzales M, Hoeffel JC, Le Merrer M, Maroteaux P, Encha-Razavi F, Joye N, Berchel C, Fliegel C, Aughton DJ, Beaudry-Rodgers K, Hasteh F, Nerlich AG, Wilcox WR, Rimoin DL, Lachman RS, Freisinger P. Elliott AM, et al. Among authors: le merrer m. Am J Med Genet. 2002 Apr 22;109(2):139-48. doi: 10.1002/ajmg.10324. Am J Med Genet. 2002. PMID: 11977163

8

Cartilage hair hypoplasia in infancy: a misleading chondrodysplasia.

Le Merrer M, Maroteaux P. Le Merrer M, et al. Eur J Pediatr. 1991 Oct;150(12):847-51. doi: 10.1007/BF01955006. Eur J Pediatr. 1991. PMID: 1743218

9

Genochondromatosis.

Le Merrer M, Fressinger P, Maroteaux P. Le Merrer M, et al. J Med Genet. 1991 Jul;28(7):485-9. doi: 10.1136/jmg.28.7.485. J Med Genet. 1991. PMID: 1895320 Free PMC article.

10

Dwarfism with gloomy face: a new syndrome with features of 3-M syndrome.

Le Merrer M, Brauner R, Maroteaux P. Le Merrer M, et al. J Med Genet. 1991 Mar;28(3):186-91. doi: 10.1136/jmg.28.3.186. J Med Genet. 1991. PMID: 2051454 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

348 results

Search Page

Filters