Verloes A - Search Results

1

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.

2

New oral-acral syndrome with partial agenesis of the maxillary bones.

Verloes A, Koulischer L. Verloes A, et al. Am J Med Genet. 1992 Nov 15;44(5):605-7. doi: 10.1002/ajmg.1320440514. Am J Med Genet. 1992. PMID: 1481817

3

Glaucoma-lens ectopia-microspherophakia-stiffness-shortness (GEMSS) syndrome: a dominant disease with manifestations of Weill-Marchesani syndromes.

Verloes A, Hermia JP, Galand A, Koulischer L, Dodinval P. Verloes A, et al. Am J Med Genet. 1992 Sep 1;44(1):48-51. doi: 10.1002/ajmg.1320440112. Am J Med Genet. 1992. PMID: 1519650

4

The orocraniodigital syndrome of Juberg and Hayward.

Verloes A, Le Merrer M, Davin JC, Wittamer P, Abrassart C, Bricteux G, Briard ML. Verloes A, et al. J Med Genet. 1992 Apr;29(4):262-5. doi: 10.1136/jmg.29.4.262. J Med Genet. 1992. PMID: 1583649 Free PMC article. Review.

5

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.

6

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.

7

Variability versus heterogeneity in syndromal hypothalamic hamartoblastoma and related disorders: review and delineation of the cerebro-acro-visceral early lethality (CAVE) multiplex syndrome.

Verloes A, Gillerot Y, Langhendries JP, Fryns JP, Koulischer L. Verloes A, et al. Am J Med Genet. 1992 Jul 1;43(4):669-77. doi: 10.1002/ajmg.1320430404. Am J Med Genet. 1992. PMID: 1621756 Review.

8

Lumping of CFC and Baraitser-Patton Noonan-like syndromes.

Verloes A, Le Merrer M. Verloes A, et al. Am J Med Genet. 1992 Mar 1;42(5):756-7. doi: 10.1002/ajmg.1320420529. Am J Med Genet. 1992. PMID: 1632454 No abstract available.

9

Mental retardation with blepharo-naso-facial abnormalities and hand malformations: a new syndrome?

van Maldergem L, Wetzburger C, Verloes A, Fourneau C, Gillerot Y. van Maldergem L, et al. Among authors: verloes a. Clin Genet. 1992 Jan;41(1):22-4. doi: 10.1111/j.1399-0004.1992.tb03622.x. Clin Genet. 1992. PMID: 1633641

10

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.

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