Verloes A - Search Results

1

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

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

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.

4

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.

5

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.

6

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.

7

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

8

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.

9

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.

10

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

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