Fryns JP - Search Results

1

Mesomelic form of chondrodysplasia and congenital glaucoma associated with de novo translocation (13;18)(q14;q23).

Dimitrov B, Devriendt K, Maas NM, Vermeesch JR, Zahariev D, Avdjieva D, Popova A, Fryns JP, Simeonov E. Dimitrov B, et al. Among authors: fryns jp. Genet Couns. 2004;15(2):191-7. Genet Couns. 2004. PMID: 15287419 Review.

2

Localization by FISH of centric fission breakpoints in a de novo trisomy 9p patient with i(9p) and t(9q;11p).

Petit P, Devriendt K, Vermeesch JR, Meireleire J, Fryns JP. Petit P, et al. Among authors: fryns jp. Genet Couns. 1998;9(3):215-21. Genet Couns. 1998. PMID: 9777345

3

Children with a 22q11 deletion versus children with a speech-language impairment and learning disability: behavior during primary school age.

Swillen A, Devriendt K, Ghesquière P, Fryns JP. Swillen A, et al. Among authors: fryns jp. Genet Couns. 2001;12(4):309-17. Genet Couns. 2001. PMID: 11837599

4

Small terminal 10q26 deletion in a male patient with Noonan-like stigmata: diagnosis by cytogenetic and FISH analysis.

Lukusa T, Smeets E, Vermeesch JR, Fryns JP. Lukusa T, et al. Among authors: fryns jp. Genet Couns. 2002;13(4):417-25. Genet Couns. 2002. PMID: 12558112

5

Partial monosomy 11q and trisomy 12q: variable expression in two siblings.

Lukusa T, Holvoet M, Vermeesch JR, Devriendt K, Fryns JP. Lukusa T, et al. Among authors: fryns jp. Genet Couns. 2003;14(2):155-64. Genet Couns. 2003. PMID: 12872809

6

Deletion 2q37.3 and autism: molecular cytogenetic mapping of the candidate region for autistic disorder.

Lukusa T, Vermeesch JR, Holvoet M, Fryns JP, Devriendt K. Lukusa T, et al. Among authors: fryns jp. Genet Couns. 2004;15(3):293-301. Genet Couns. 2004. PMID: 15517821

7

De novo deletion 7q36 resulting from a distal 7q/8q translocation: phenotypic expression and comparison to the literature.

Lukusa T, Vermeesch JR, Fryns JP. Lukusa T, et al. Among authors: fryns jp. Genet Couns. 2005;16(1):1-15. Genet Couns. 2005. PMID: 15844773 Review.

8

Partial trisomy 9q syndrome with a de novo tandem duplication of 9q22.2-q31.1.

Utine GE, Melotte C, Vermeesch JR, Fryns JP. Utine GE, et al. Among authors: fryns jp. Genet Couns. 2005;16(4):407-12. Genet Couns. 2005. PMID: 16440884

9

The t(4;8) is mediated by homologous recombination between olfactory receptor gene clusters, but other 4p16 translocations occur at random.

Maas NM, Van Vooren S, Hannes F, Van Buggenhout G, Mysliwiec M, Moreau Y, Fagan K, Midro A, Engiz O, Balci S, Parker MJ, Sznajer Y, Devriendt K, Fryns JP, Vermeesch JR. Maas NM, et al. Among authors: fryns jp. Genet Couns. 2007;18(4):357-65. Genet Couns. 2007. PMID: 18286816

10

A cryptic duplication 22q13.31 to qter leads to a distinct phenotype with mental retardation, microcephaly and mild facial dysmorphism.

Peeters H, Vermeesch J, Fryns JP. Peeters H, et al. Among authors: fryns jp. Genet Couns. 2008;19(4):365-71. Genet Couns. 2008. PMID: 19239079

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