Verloes A - Search Results

1

Spondylometaphyseal dysplasia, east-African type: a new form of early, severe SMD with rounded vertebrae.

Verloes A, Lepage P, Baumann C, Maroteaux P, Merrer ML. Verloes A, et al. Am J Med Genet. 2002 Dec 15;113(4):362-6. doi: 10.1002/ajmg.b.10738. Am J Med Genet. 2002. PMID: 12457408

2

Metaphyseal acroscyphodysplasia.

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

3

Metaphyseal anadysplasia: a metaphyseal dysplasia of early onset with radiological regression and benign course.

Maroteaux P, Verloes A, Stanescu V, Stanescu R. Maroteaux P, et al. Among authors: verloes a. Am J Med Genet. 1991 Apr 1;39(1):4-10. doi: 10.1002/ajmg.1320390103. Am J Med Genet. 1991. PMID: 1867263

4

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. 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.

5

Microspherophakia-metaphyseal dysplasia: a 'new' dominantly inherited bone dysplasia with severe eye involvement.

Verloes A, Van Maldergem L, de Marneffe P, Dufier JL, Maroteaux P. Verloes A, et al. J Med Genet. 1990 Jul;27(7):467-71. doi: 10.1136/jmg.27.7.467. J Med Genet. 1990. PMID: 2395168 Free PMC article.

6

BBBG syndrome or Opitz syndrome: new family.

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

7

Osteocraniostenosis.

Verloes A, Narcy F, Grattagliano B, Delezoide AL, Guibaud P, Schaaps JP, Le Merrer M, Maroteaux P. Verloes A, et al. 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.

8

Koraxitrachitic syndrome: a syndromic form of self-healing collodion baby with residual dappled atrophy of the derma.

Verloes A, Hermanns-Lê T, Lesenfants S, Lombet J, Lamotte PJ, Crèvecoeur-Liégeois C, Duchesne B, Piérard GE. Verloes A, et al. Am J Med Genet. 1999 Oct 29;86(5):454-8. Am J Med Genet. 1999. PMID: 10508988

9

Fronto-otopalatodigital osteodysplasia: clinical evidence for a single entity encompassing Melnick-Needles syndrome, otopalatodigital syndrome types 1 and 2, and frontometaphyseal dysplasia.

Verloes A, Lesenfants S, Barr M, Grange DK, Journel H, Lombet J, Mortier G, Roeder E. Verloes A, et al. Am J Med Genet. 2000 Feb 28;90(5):407-22. doi: 10.1002/(sici)1096-8628(20000228)90:5<407::aid-ajmg11>3.0.co;2-d. Am J Med Genet. 2000. PMID: 10706363

10

New dysostosis showing multilevel absence of vertebral pedicles: unique developmental anomaly of vertebral arches?

Verloes A, Muller C, Philippet P. Verloes A, et al. Am J Med Genet. 2000 Dec 18;95(5):473-6. Am J Med Genet. 2000. PMID: 11146469

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