Briard ML - Search Results

1

[Variable expression of an autosomal dominant syndrome: (BBB syndrome or G syndrome)].

Le Merrer M, Verloes A, Narcy P, Briard ML. Le Merrer M, et al. Among authors: briard ml. J Genet Hum. 1988 Jun;36(3):257-64. J Genet Hum. 1988. PMID: 3411306 French.

2

Ophthalmo-acromelic syndrome.

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

3

[Genetic counseling in craniostenosis. Results of a prospective study performed with a group of studies on craniofacial malformations].

Le Merrer M, Ledinot V, Renier D, Marchac D, Briard ML. Le Merrer M, et al. Among authors: briard ml. J Genet Hum. 1988 Aug;36(4):295-306. J Genet Hum. 1988. PMID: 3221205 French.

4

BBBG syndrome or Opitz syndrome: new family.

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

5

[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. Among authors: briard ml. J Genet Hum. 1989 Jun;37(2):163-5. J Genet Hum. 1989. PMID: 2746174 French. No abstract available.

6

CFC syndrome: a syndrome distinct from Noonan syndrome.

Verloes A, Le Merrer M, Soyeur D, Kaplan J, Pangalos C, Rigo J, Briard ML. Verloes A, et al. Among authors: briard ml. Ann Genet. 1988;31(4):230-4. Ann Genet. 1988. PMID: 3265306

7

[An unrecognized etiology of sexual ambiguity: Smith-Lemli-Opitz syndrome or a new entity?].

Le Merrer M, Briard ML, Chauvet ML. Le Merrer M, et al. Among authors: briard ml. J Genet Hum. 1987 May;35(2-3):187-93. J Genet Hum. 1987. PMID: 3612097 French.

8

[Malformation uropathies and multiple malformation syndromes].

Briard ML, Le Merrer M, Kaplan J, Bois E, Frézal J. Briard ML, et al. J Genet Hum. 1984 Jun;32(2):83-90. J Genet Hum. 1984. PMID: 6736939 French.

9

Lethal progeroid syndrome with osteolysis. Case report.

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

10

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. Among authors: briard ml. Genet Couns. 1991;2(4):233-6. Genet Couns. 1991. PMID: 1799422

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