Maroteaux P - Search Results

1

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. Among authors: maroteaux p. 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.

2

Metaphyseal acroscyphodysplasia.

Verloes A, Le Merrer M, Farriaux JP, Maroteaux P. Verloes A, et al. Among authors: maroteaux p. 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. 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. Among authors: maroteaux p. 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

Osteocraniostenosis.

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

6

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. Among authors: maroteaux p. Am J Med Genet. 2002 Dec 15;113(4):362-6. doi: 10.1002/ajmg.b.10738. Am J Med Genet. 2002. PMID: 12457408

7

The gene for hereditary multiple exostoses does not map to the Langer-Giedion region (8q23-q24).

Le Merrer M, Ben Othmane K, Stanescu V, Lyonnet S, Van Maldergem L, Royer G, Munnich A, Maroteaux P. Le Merrer M, et al. Among authors: maroteaux p. J Med Genet. 1992 Oct;29(10):713-5. doi: 10.1136/jmg.29.10.713. J Med Genet. 1992. PMID: 1433231 Free PMC article.

8

Micromelic dwarfism with cone epiphyses, metaphyseal dysplasia, and vertebral segmentation defects.

Fryns JP, Lorenzetti ME, Maroteaux P, Van den Berghe H. Fryns JP, et al. Among authors: maroteaux p. Am J Med Genet. 1996 Jan 11;61(2):164-7. doi: 10.1002/(SICI)1096-8628(19960111)61:2<164::AID-AJMG12>3.0.CO;2-S. Am J Med Genet. 1996. PMID: 8669445

9

[Optic atrophy in children in Pyle's craniometaphyseal dysplasia].

Auclin F, Dufier JL, Manderieux N, Sitruk F, Benoît B, Maroteaux P, Couly G, Aicardi J, Haye C. Auclin F, et al. Among authors: maroteaux p. Bull Soc Ophtalmol Fr. 1989 Aug-Sep;89(8-9):923-4. Bull Soc Ophtalmol Fr. 1989. PMID: 2620431 French. No abstract available.

10

Diaphanospondylodysostosis (DSD): confirmation of a recessive disorder with abnormal vertebral ossification and nephroblastomatosis.

Gonzales M, Verloes A, Saint Frison MH, Perrotez C, Bourdet O, Encha-Razavi F, Joyé N, Taillemite JL, Walbaum R, Pfeiffer R, Maroteaux P. Gonzales M, et al. Among authors: maroteaux p. Am J Med Genet A. 2005 Aug 1;136A(4):373-6. doi: 10.1002/ajmg.a.30537. Am J Med Genet A. 2005. PMID: 15988748

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