de Cock P - Search Results

1

Pathogenesis of vestibular schwannoma in ring chromosome 22.

Denayer E, Brems H, de Cock P, Evans GD, Van Calenbergh F, Bowers N, Sciot R, Debiec-Rychter M, Vermeesch JV, Fryns JP, Legius E. Denayer E, et al. Among authors: de cock p. BMC Med Genet. 2009 Sep 22;10:97. doi: 10.1186/1471-2350-10-97. BMC Med Genet. 2009. PMID: 19772601 Free PMC article.

2

Inverted distal duplication of the long arm of chromosome 8: borderline intelligence and discrete dysmorphic syndrome.

Kleczkowska A, Fryns JP, Decock P, Van den Berghe H. Kleczkowska A, et al. Genet Couns. 1991;2(2):109-13. Genet Couns. 1991. PMID: 1781954

3

Mosaic normal/15q11-q13 duplication associated with developmental delay but normal phenotype.

Goossens E, Decock P, Potgieter S, Fryns JP. Goossens E, et al. Genet Couns. 1999;10(2):133-6. Genet Couns. 1999. PMID: 10422005

4

Occipital scalp defect associated with valvular pulmonary stenosis. A new entity?

Fryns JP, de Cock P, van den Berghe H. Fryns JP, et al. Among authors: de cock p. Clin Genet. 1992 Aug;42(2):97-9. doi: 10.1111/j.1399-0004.1992.tb03147.x. Clin Genet. 1992. PMID: 1424238

5

Direct duplication 16q11.1----16q13 is not associated with a typical dysmorphic syndrome.

Fryns JP, Kleczkowska A, Decock P, Van den Berghe H. Fryns JP, et al. Ann Genet. 1990;33(1):46-8. Ann Genet. 1990. PMID: 2195981 Review.

6

Partial duplication of the short arm of chromosome 2 (dup(2)(p13----p21) associated with mental retardation and an Aarskog-like phenotype.

Fryns JP, Kleczkowska A, Kenis H, Decock P, Van den Berghe H. Fryns JP, et al. Ann Genet. 1989;32(3):174-6. Ann Genet. 1989. PMID: 2573314

7

Costello syndrome: the natural history of a true postnatal growth retardation syndrome.

Umans S, Decock P, Fryns JP. Umans S, et al. Genet Couns. 1995;6(2):121-5. Genet Couns. 1995. PMID: 7546454

8

Terminal deletion in chromosome region 8p23.1-8pter in a child with features of velo-cardio-facial syndrome.

Devriendt K, De Mars K, De Cock P, Gewillig M, Fryns JP. Devriendt K, et al. Among authors: de cock p, de mars k. Ann Genet. 1995;38(4):228-30. Ann Genet. 1995. PMID: 8629811

9

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.

10

Unusual de novo t(13;15)(q12.1;p13) translocation leading to complex mosaicism including jumping translocation.

Petit P, Devriendt K, Vermeesch JR, De Cock P, Fryns JP. Petit P, et al. Among authors: de cock p. Ann Genet. 1998;41(1):22-6. Ann Genet. 1998. PMID: 9599647

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