Decock P - Search Results

1

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. Among authors: decock p. Ann Genet. 1989;32(3):174-6. Ann Genet. 1989. PMID: 2573314

2

46,XX/46,XX,del(20)(pter-->p12.2) mosaicism limited to fibroblasts associated with MCA/MR and severe growth deficit.

Fryns JP, Kleczkowska A, Decock P, Massa G, van den Berghe H. Fryns JP, et al. Among authors: decock p. Ann Genet. 1992;35(4):234-6. Ann Genet. 1992. PMID: 1296522

3

Severe pre- and postnatal growth retardation, developmental delay with hypotonia and marked hypotrophy of the distal extremities, dental anomalies, and eczematous skin. A new autosomal recessive entity.

Grubben C, de Cock P, Borghgraef M, van den Berghe H, Fryns JP. Grubben C, et al. Clin Genet. 1992 Jan;41(1):16-21. doi: 10.1111/j.1399-0004.1992.tb03621.x. Clin Genet. 1992. PMID: 1378778

4

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. Among authors: decock p. Genet Couns. 1991;2(2):109-13. Genet Couns. 1991. PMID: 1781954

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. Among authors: decock p. Ann Genet. 1990;33(1):46-8. Ann Genet. 1990. PMID: 2195981 Review.

6

Angelman's syndrome and 15q11-q13 deletion.

Fryns JP, Kleczowska A, Decock P, van den Berghe H. Fryns JP, et al. Among authors: decock p. Genet Couns. 1990;1(1):57-62. Genet Couns. 1990. PMID: 2222923

7

De novo paracentric inversion in a microcephalic boy: 46,XY, inv(14)(q13q24).

Jaeken J, Fryns JP, Standaert L, De Cock P, Van den Berghe H. Jaeken J, et al. Ann Genet. 1980;23(2):105-7. Ann Genet. 1980. PMID: 6967281

8

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

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

9

Borderline intelligence and discrete craniofacial dysmorphism in an adolescent female with partial trisomy 7p due to a de novo tandem duplication 7 (p15.1-->p21.3).

Kleczkowska A, Decock P, van den Berghe H, Fryns JP. Kleczkowska A, et al. Among authors: decock p. Genet Couns. 1994;5(4):393-7. Genet Couns. 1994. PMID: 7888144 No abstract available.

10

Complex chromosomal rearrangement (CCR), moderate mental retardation and discrete dysmorphic syndrome.

Kleczkowska A, Fryns JP, Decock P, Van den Berghe H. Kleczkowska A, et al. Among authors: decock p. Genet Couns. 1993;4(4):321-4. Genet Couns. 1993. PMID: 8110421 No abstract available.

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