Verloes A - Search Results

1

Inversion duplication deletions involving the long arm of chromosome 13: phenotypic description of additional three fetuses and genotype-phenotype correlation.

Quelin C, Spaggiari E, Khung-Savatovsky S, Dupont C, Pasquier L, Loeuillet L, Jaillard S, Lucas J, Marcorelles P, Journel H, Pluquailec-Bilavarn K, Bazin A, Verloes A, Delezoide AL, Aboura A, Guimiot F. Quelin C, et al. Among authors: verloes a. Am J Med Genet A. 2014 Oct;164A(10):2504-9. doi: 10.1002/ajmg.a.36658. Epub 2014 Jun 26. Am J Med Genet A. 2014. PMID: 24975584

2

Osteocraniostenosis.

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.

3

Monosomy 11q: report of two familial cases and review of the literature.

Hustinx R, Verloes A, Grattagliano B, Herens C, Jamar M, Soyeur D, Schaaps JP, Koulischer L. Hustinx R, et al. Among authors: verloes a. Am J Med Genet. 1993 Sep 1;47(3):312-7. doi: 10.1002/ajmg.1320470303. Am J Med Genet. 1993. PMID: 8135272 Review.

4

Heterogeneity versus variability in megalocornea-mental retardation (MMR) syndromes: report of new cases and delineation of 4 probable types.

Verloes A, Journel H, Elmer C, Misson JP, Le Merrer M, Kaplan J, Van Maldergem L, Deconinck H, Meire F. Verloes A, et al. Am J Med Genet. 1993 Apr 15;46(2):132-7. doi: 10.1002/ajmg.1320460206. Am J Med Genet. 1993. PMID: 8484397 Review.

5

Opitz GBBB syndrome: chromosomal evidence of an X-linked form.

Verloes A, David A, Odent S, Toutain A, André MJ, Lucas J, Le Marec B. Verloes A, et al. Am J Med Genet. 1995 Oct 23;59(1):123-8. doi: 10.1002/ajmg.1320590124. Am J Med Genet. 1995. PMID: 8849003

6

Fronto-otopalatodigital osteodysplasia: clinical evidence for a single entity encompassing Melnick-Needles syndrome, otopalatodigital syndrome types 1 and 2, and frontometaphyseal dysplasia.

Verloes A, Lesenfants S, Barr M, Grange DK, Journel H, Lombet J, Mortier G, Roeder E. Verloes A, et al. Am J Med Genet. 2000 Feb 28;90(5):407-22. doi: 10.1002/(sici)1096-8628(20000228)90:5<407::aid-ajmg11>3.0.co;2-d. Am J Med Genet. 2000. PMID: 10706363

7

Mosaic trisomy 15 and hemihypertrophy.

Gérard-Blanluet M, Elbez A, Bazin A, Danan C, Verloes A, Janaud JC. Gérard-Blanluet M, et al. Among authors: verloes a. Ann Genet. 2001 Jul-Sep;44(3):143-8. doi: 10.1016/s0003-3995(01)01080-2. Ann Genet. 2001. PMID: 11694227

8

CGH and direct diagnosis of mosaic structural chromosomal abnormalities: description of a mosaic ring chromosome 17 and review of the literature.

Dupont C, Pipiras E, Chantot-Bastaraud S, Verloes A, Baumann C, Wolf JP, Benzacken B. Dupont C, et al. Among authors: verloes a. Eur J Hum Genet. 2003 Jun;11(6):452-6. doi: 10.1038/sj.ejhg.5200984. Eur J Hum Genet. 2003. PMID: 12774038

9

Further delineation of the congenital form of X-linked dyskeratosis congenita (Hoyeraal-Hreidarsson syndrome).

Sznajer Y, Baumann C, David A, Journel H, Lacombe D, Perel Y, Blouin P, Segura JF, Cezard JP, Peuchmaur M, Vulliamy T, Dokal I, Verloes A. Sznajer Y, et al. Among authors: verloes a. Eur J Pediatr. 2003 Dec;162(12):863-7. doi: 10.1007/s00431-003-1317-5. Epub 2003 Sep 30. Eur J Pediatr. 2003. PMID: 14648217 Review.

10

Three patients with hallucal polydactyly and WAGR syndrome, including discordant expression of Wilms tumor in MZ twins.

Brémond-Gignac D, Gérard-Blanluet M, Copin H, Bitoun P, Baumann C, Crolla JA, Benzacken B, Verloes A. Brémond-Gignac D, et al. Among authors: verloes a. Am J Med Genet A. 2005 May 1;134(4):422-5. doi: 10.1002/ajmg.a.30646. Am J Med Genet A. 2005. PMID: 15779023

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