le Merrer M - Search Results

1

[Autosomal recessive metaphyseal chondrodysplasia and Hirschsprung's disease].

le Merrer M, Briard ML, Chauvet ML, Maroteaux P. le Merrer M, et al. Ann Pediatr (Paris). 1991 Jan;38(1):27-30. Ann Pediatr (Paris). 1991. PMID: 2006830 French.

2

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

3

Lethal progeroid syndrome with osteolysis. Case report.

Le Merrer M, Guillot M, Briard ML, Maroteaux P. Le Merrer M, et al. Ann Genet. 1991;34(2):82-4. Ann Genet. 1991. PMID: 1746888

4

Scalp defect, nipples absence and ears abnormalities: an other case of Finlay syndrome.

Le Merrer M, Renier D, Briard ML. Le Merrer M, et al. Genet Couns. 1991;2(4):233-6. Genet Couns. 1991. PMID: 1799422

5

Desbuquois syndrome.

Le Merrer M, Young ID, Stanescu V, Maroteaux P. Le Merrer M, et al. Eur J Pediatr. 1991 Sep;150(11):793-6. doi: 10.1007/BF02026714. Eur J Pediatr. 1991. PMID: 1959544

6

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.

7

BBBG syndrome or Opitz syndrome: new family.

Verloes A, Le Merrer M, Briard ML. Verloes A, et al. Among authors: le merrer m. Am J Med Genet. 1989 Nov;34(3):313-6. doi: 10.1002/ajmg.1320340303. Am J Med Genet. 1989. PMID: 2688419 Review.

8

[Golabi Rosen syndrome: a rare syndrome with imprecise nosologic limits, failure of prenatal diagnosis].

Le Merrer M, Roume J, Narcy F, Larroche JC, Briard ML. Le Merrer M, et al. J Genet Hum. 1989 Jun;37(2):163-5. J Genet Hum. 1989. PMID: 2746174 French. No abstract available.

9

Acrofacial dysostoses.

Le Merrer M, Cikuli M, Ribier J, Briard ML. Le Merrer M, et al. Am J Med Genet. 1989 Jul;33(3):318-22. doi: 10.1002/ajmg.1320330307. Am J Med Genet. 1989. PMID: 2801764

10

Ophthalmo-acromelic syndrome.

Le Merrer M, Nessmann C, Briard ML, Maroteaux P. Le Merrer M, et al. Ann Genet. 1988;31(4):226-9. Ann Genet. 1988. PMID: 3146242

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