Hamel B - 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. Among authors: hamel b. Genet Couns. 1998;9(3):201-4. Genet Couns. 1998. PMID: 9777342

2

13q deletion syndrome in an adult mentally retarded patient.

Van Buggenhout G, Trommelen J, Hamel B, Fryns JP. Van Buggenhout G, et al. Among authors: hamel b. Genet Couns. 1999;10(2):177-81. Genet Couns. 1999. PMID: 10422012 Review.

3

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

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

4

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: hamel bc. Genet Couns. 1996;7(3):177-86. Genet Couns. 1996. PMID: 8897038

5

Down syndrome in a population of elderly mentally retarded patients: genetic-diagnostic survey and implications for medical care.

Van Buggenhout GJ, Trommelen JC, Schoenmaker A, De Bal C, Verbeek JJ, Smeets DF, Ropers HH, Devriendt K, Hamel BC, Fryns JP. Van Buggenhout GJ, et al. Among authors: hamel bc. Am J Med Genet. 1999 Aug 6;85(4):376-84. doi: 10.1002/(sici)1096-8628(19990806)85:4<376::aid-ajmg14>3.3.co;2-h. Am J Med Genet. 1999. PMID: 10398264

6

Angelman syndrome in three adult patients with atypical presentation and severe neurological complications.

Van Buggenhout GJ, Descheemaeker MJ, Thiry P, Trommelen JC, Hamel BC, Fryns JP. Van Buggenhout GJ, et al. Among authors: hamel bc. Genet Couns. 2000;11(4):363-73. Genet Couns. 2000. PMID: 11140414

7

Metabolic studies in older mentally retarded patients: significance of metabolic testing and correlation with the clinical phenotype.

Van Buggenhout GJ, Trijbels JM, Wevers R, Trommelen JC, Hamel BC, Brunner HG, Fryns JP. Van Buggenhout GJ, et al. Among authors: hamel bc. Genet Couns. 2001;12(1):1-21. Genet Couns. 2001. PMID: 11332972

8

The clinical phenotype in institutionalised adult males with X-linked mental retardation (XLMR).

Van Buggenhout GJ, Trommelen JC, Brunner HG, Hamel BC, Fryns J. Van Buggenhout GJ, et al. Among authors: hamel bc. Ann Genet. 2001 Jan-Mar;44(1):47-55. doi: 10.1016/s0003-3995(01)01038-3. Ann Genet. 2001. PMID: 11334618

9

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

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

10

9th international workshop on fragile X syndrome and X-linked mental retardation.

Fryns JP, Borghgraef M, Brown TW, Chelly J, Fisch GS, Hamel B, Hanauer A, Lacombe D, Luo L, MacPherson JN, Mandel JL, Moraine C, Mulley J, Nelson D, Oostra B, Partington M, Ramakers GJ, Ropers HH, Rousseau F, Schwartz C, Steinbach P, Stoll C, Tranebjaerg L, Turner G, Van Bokhoven H, Vianna-Morgante A. Fryns JP, et al. Among authors: hamel b. Am J Med Genet. 2000 Oct 23;94(5):345-60. doi: 10.1002/1096-8628(20001023)94:5<345::aid-ajmg1>3.0.co;2-z. Am J Med Genet. 2000. PMID: 11050616 No abstract available.

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