Verloes A - Search Results

1

Lissencephaly type III, stippled epiphyses and loose, thick skin: a new recessively inherited syndrome.

Plauchu H, Encha-Razavi F, Hermier M, Attia-Sobol J, Vitrey D, Verloes A. Plauchu H, et al. Among authors: verloes a. Am J Med Genet. 2001 Feb 15;99(1):14-20. doi: 10.1002/1096-8628(20010215)99:1<14::aid-ajmg1121>3.0.co;2-s. Am J Med Genet. 2001. PMID: 11170088

2

The Baller-Gerold syndrome.

Van Maldergem L, Verloes A, Lejeune L, Gillerot Y. Van Maldergem L, et al. Among authors: verloes a. J Med Genet. 1992 Apr;29(4):266-8. doi: 10.1136/jmg.29.4.266. J Med Genet. 1992. PMID: 1583650 Free PMC article.

3

Restrictive dermopathy, a lethal form of arthrogryposis multiplex with skin and bone dysplasias: three new cases and review of the literature.

Verloes A, Mulliez N, Gonzales M, Laloux F, Hermanns-Lê T, Piérard GE, Koulischer L. Verloes A, et al. Am J Med Genet. 1992 Jun 1;43(3):539-47. doi: 10.1002/ajmg.1320430308. Am J Med Genet. 1992. PMID: 1605246 Review.

4

Acromelic frontonasal "dysplasia": further delineation of a subtype with brain malformation and polydactyly (Toriello syndrome).

Verloes A, Gillerot Y, Walczak E, Van Maldergem L, Koulischer L. Verloes A, et al. Am J Med Genet. 1992 Jan 15;42(2):180-3. doi: 10.1002/ajmg.1320420209. Am J Med Genet. 1992. PMID: 1733166 Review.

5

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. 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.

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

Albinism and agenesis of the corpus callosum with profound developmental delay: Vici syndrome, evidence for autosomal recessive inheritance.

del Campo M, Hall BD, Aeby A, Nassogne MC, Verloes A, Roche C, Gonzalez C, Sanchez H, Garcia-Alix A, Cabanas F, Escudero RM, Hernandez R, Quero J. del Campo M, et al. Among authors: verloes a. Am J Med Genet. 1999 Aug 27;85(5):479-85. doi: 10.1002/(sici)1096-8628(19990827)85:5<479::aid-ajmg9>3.3.co;2-4. Am J Med Genet. 1999. PMID: 10405446 Review.

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

Microphthalmia, facial anomalies, microcephaly, thumb and hallux hypoplasia, and agammaglobulinemia.

Verloes A, Dresse MF, Keutgen H, Asplund C, Smith CI. Verloes A, et al. Am J Med Genet. 2001 Jul 1;101(3):209-12. doi: 10.1002/ajmg.1373. Am J Med Genet. 2001. PMID: 11424135

10

Clinical and genetic heterogeneity of Seckel syndrome.

Faivre L, Le Merrer M, Lyonnet S, Plauchu H, Dagoneau N, Campos-Xavier AB, Attia-Sobol J, Verloes A, Munnich A, Cormier-Daire V. Faivre L, et al. Among authors: verloes a. Am J Med Genet. 2002 Nov 1;112(4):379-83. doi: 10.1002/ajmg.10677. Am J Med Genet. 2002. PMID: 12376940

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