Vamos E - Search Results

1

Characterization of Deletions of the HBA and HBB Loci by Array Comparative Genomic Hybridization.

Sabath DE, Bender MA, Sankaran VG, Vamos E, Kentsis A, Yi HS, Greisman HA. Sabath DE, et al. Among authors: vamos e. J Mol Diagn. 2016 Jan;18(1):92-9. doi: 10.1016/j.jmoldx.2015.07.011. Epub 2015 Nov 21. J Mol Diagn. 2016. PMID: 26612711 Free PMC article.

2

Prenatal diagnosis of a constitutional interstitial deletion of chromosome 5 (q15q31.1) presenting with features of congenital contractural arachnodactyly.

Courtens W, Tjalma W, Messiaen L, Vamos E, Martin JJ, Van Bogaert E, Keersmaekers G, Meulyzer P, Wauters J. Courtens W, et al. Among authors: vamos e. Am J Med Genet. 1998 May 18;77(3):188-97. Am J Med Genet. 1998. PMID: 9605585

3

Interstitial deletion 2q33.3-q34 in a boy with a phenotype resembling the Seckel syndrome.

Courtens W, Speleman F, Messiaen L, Bormans J, Van Roy N, Vamos E. Courtens W, et al. Among authors: vamos e. Am J Med Genet. 1997 Sep 5;71(4):479-85. Am J Med Genet. 1997. PMID: 9286460 Review.

4

Chromosomal findings in cultured melanocytes from a giant congenital nevus.

Heimann P, Ogur G, De Busscher C, Morandini R, Libert A, Vamos E. Heimann P, et al. Among authors: vamos e. Cancer Genet Cytogenet. 1993 Jul 1;68(1):74-7. doi: 10.1016/0165-4608(93)90077-y. Cancer Genet Cytogenet. 1993. PMID: 8330286

5

[The value of prenatal chromosomal diagnosis in cases of fetal abnormalities: results obtained in 468 pathological pregnancies].

Vamos E, Elmer C, Lévi S, el Khazen N, Donner C, Avni F, Rodesch F. Vamos E, et al. Rev Med Brux. 1990 Jun;11(6):231-5. Rev Med Brux. 1990. PMID: 2371470 French.

6

Severe congenital cutis laxa with pulmonary emphysema: a family with three affected sibs.

Van Maldergem L, Vamos E, Liebaers I, Petit P, Vandevelde G, Simonis-Blumenfrucht A, Bouffioux R, Kulakowski S, Hanquinet S, Van Durme P, et al. Van Maldergem L, et al. Among authors: vamos e. Am J Med Genet. 1988 Oct;31(2):455-64. doi: 10.1002/ajmg.1320310226. Am J Med Genet. 1988. PMID: 3232707

7

[Cordocentesis: experience in 391 initial samples].

Donner C, Simon P, Gosselin F, Vermeylen D, Avni F, Liesnard C, Vamos E, Cochaux P, Vassart G, Rodesch F. Donner C, et al. Among authors: vamos e. Rev Med Brux. 1990 Jun;11(6):217-22. Rev Med Brux. 1990. PMID: 2371468 French.

8

Cordocentesis for rapid karyotype: 421 consecutive cases.

Donner C, Rypens F, Paquet V, Cohen E, Delneste D, van Regemorter N, Vamos E, Avni F, Rodesch F. Donner C, et al. Among authors: vamos e. Fetal Diagn Ther. 1995 May-Jun;10(3):192-9. doi: 10.1159/000264235. Fetal Diagn Ther. 1995. PMID: 7639943

9

Familial trisomy 11p resulting from a balanced paternal translocation: 3 new cases including first trimester diagnosis.

Ogur G, Hayez F, Herinckx A, Van Regemorter N, Vamos E. Ogur G, et al. Among authors: vamos e. J Genet Hum. 1988 Aug;36(4):323-9. J Genet Hum. 1988. PMID: 3221208

10

[Prenatal diagnosis using amniocentesis and chorionic villi sampling: comparative study of chromosomal findings].

Vamos E, Hayez-Delatte F, Van Regemorter N, Rodesch F. Vamos E, et al. Rev Med Brux. 1990 Jun;11(6):223-30. Rev Med Brux. 1990. PMID: 2371469 French.

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