Verloes A - Search Results

1

Heterogeneity of SPONASTRIME dysplasia: delineation of a variant form with severe mental retardation.

Verloes A, Misson JP, Dubru JM, Jamblin P, Le Merrer M. Verloes A, et al. Clin Dysmorphol. 1995 Jul;4(3):208-15. Clin Dysmorphol. 1995. PMID: 7551156

2

Sjögren-Larsson-like syndrome with bone dysplasia and normal fatty alcohol NAD+ oxidoreductase activity.

Scalais E, Verloes A, Sacré JP, Piérard GE, Rizzo WB. Scalais E, et al. Among authors: verloes a. Pediatr Neurol. 1992 Nov-Dec;8(6):459-65. doi: 10.1016/0887-8994(92)90010-v. Pediatr Neurol. 1992. PMID: 1476577

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

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.

5

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

6

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

7

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.

8

Male pseudohermaphroditism with persistent müllerian structures, mental retardation and Borjeson-Forssman-Lehmann-like features: a new syndrome?

Verloes A, Gillerot Y, Delfortrie J, Zeevaert-Arnold MT, Collard R, Koulischer L, Fryns JP. Verloes A, et al. Genet Couns. 1990;1(3-4):219-25. Genet Couns. 1990. PMID: 2098045

9

Lambotte syndrome: microcephaly, holoprosencephaly, intrauterine growth retardation, facial anomalies, and early lethality--a new sublethal multiple congenital anomaly/mental retardation syndrome in four sibs.

Verloes A, Dodinval P, Beco L, Bonnivert J, Lambotte C. Verloes A, et al. Am J Med Genet. 1990 Sep;37(1):119-23. doi: 10.1002/ajmg.1320370128. Am J Med Genet. 1990. PMID: 2240028

10

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.

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