Van Buggenhout G - Search Results

1

Björnstad syndrome in a patient with mental retardation.

Van Buggenhout G, Trommelen J, Hamel B, Fryns JP. Van Buggenhout G, et al. Genet Couns. 1998;9(3):201-4. Genet Couns. 1998. PMID: 9777342

2

Early urethral obstruction sequence and trisomy of the long arm of chromosome 1.

van Buggenhout G, Cooreman G, Thienpont L, Fryns JP. van Buggenhout G, et al. Ann Genet. 1995;38(2):106-7. Ann Genet. 1995. PMID: 7486825 No abstract available.

3

Renal agenesis and trisomy 22: case report and review.

Van Buggenhout GJ, Verbruggen J, Fryns JP. Van Buggenhout GJ, et al. Ann Genet. 1995;38(1):44-8. Ann Genet. 1995. PMID: 7625758 Review.

4

Characteristic facial dysmorphism, arachnodactyly and mental retardation: another case.

Van Buggenhout GJ, Akkermans-Scholten AC, Hamel BC. Van Buggenhout GJ, et al. Genet Couns. 1995;6(1):61-3. Genet Couns. 1995. PMID: 7794564 Review. No abstract available.

5

Down-Turner syndrome: case report and review.

Van Buggenhout GJ, Hamel BC, Trommelen JC, Mieloo H, Smeets DF. Van Buggenhout GJ, et al. J Med Genet. 1994 Oct;31(10):807-10. doi: 10.1136/jmg.31.10.807. J Med Genet. 1994. PMID: 7837259 Free PMC article. Review.

6

A distinct phenotype associated with partial trisomy 10q due to proximal direct duplication 10q11 --> q223?

van Buggenhout G, Decock P, Fryns JP. van Buggenhout G, et al. Genet Couns. 1996;7(1):53-9. Genet Couns. 1996. PMID: 8652089 Review.

7

Zimmermann-Laband syndrome in a patient with severe mental retardation.

Van Buggenhout GJ, Brunner HG, Trommelen JC, Hamel BC. Van Buggenhout GJ, et al. Genet Couns. 1995;6(4):321-7. Genet Couns. 1995. PMID: 8775419 Review.

8

Fountain syndrome: further delineation of the clinical syndrome and follow-up data.

Van Buggenhout GJ, Van Ravenswaaij-Arts CM, Renier WO, Van de Wiel MP, Trommelen JC, Pijkels E, Hamel BC, Fryns JP. Van Buggenhout GJ, et al. Among authors: van ravenswaaij arts cm, van de wiel mp. Genet Couns. 1996;7(3):177-86. Genet Couns. 1996. PMID: 8897038

9

Partial trisomy 4q due to a maternal translocation: t(4;18)(q27;q21.31).

Van Buggenhout G, Moerman PH, Fryns JP. Van Buggenhout G, et al. Genet Couns. 1997;8(1):19-24. Genet Couns. 1997. PMID: 9101274

10

Chromosome healing of constitutional chromosome deletions studied by microdissection.

Vermeesch JR, Falzetti D, Van Buggenhout G, Fryns JP, Marynen P. Vermeesch JR, et al. Among authors: van buggenhout g. Cytogenet Cell Genet. 1998;81(1):68-72. doi: 10.1159/000014991. Cytogenet Cell Genet. 1998. PMID: 9691179

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