Kleczkowska A - Search Results

1

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: kleczkowska a. Ann Genet. 1990;33(1):46-8. Ann Genet. 1990. PMID: 2195981 Review.

2

High incidence of mental retardation in Turner syndrome patients with ring chromosome X formation.

Fryns JP, Kleczkowska A, Van Den Berghe H. Fryns JP, et al. Among authors: kleczkowska a. Genet Couns. 1990;1(2):161-5. Genet Couns. 1990. PMID: 2080999

3

Ring chromosome 15: follow-up data on physical and psychological development.

Fryns JP, Borghgraef M, Kleczkowska A, Van Den Berghe H. Fryns JP, et al. Among authors: kleczkowska a. Genet Couns. 1990;1(2):167-72. Genet Couns. 1990. PMID: 2081000

4

Interstitial deletion of the short arm of chromosome 12. Report of a new patient and review of the literature.

Fryns JP, Kleczkowska A, Van den Berghe H. Fryns JP, et al. Among authors: kleczkowska a. Ann Genet. 1990;33(1):43-5. Ann Genet. 1990. PMID: 2195980 Review.

5

Holoprosencephaly in a fetus with a 46,XX,der(7), t(7;8)(q36.1;p12) mat karyotype.

Kleczkowska A, Fryns JP, Moerman P, Vandenberghe K, Van den Berghe H. Kleczkowska A, et al. Ann Genet. 1990;33(2):111-2. Ann Genet. 1990. PMID: 2241084

6

Cohen syndrome and de novo reciprocal translocation t(5;7)(q33.1;p15.1).

Fryns JP, Kleczkowska A, Smeets E, Thiry P, Geutjens J, Van den Berghe H. Fryns JP, et al. Among authors: kleczkowska a. Am J Med Genet. 1990 Dec;37(4):546-7. doi: 10.1002/ajmg.1320370425. Am J Med Genet. 1990. PMID: 2260606

7

Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission. Karyotype: 46,XX,-13, +t(13;13)(p11;q11)/46,XX,del(13)(p11). A second example.

Fryns JP, Kleczkowska A, Jaeken J, Van Herck K, Van den Berghe MH. Fryns JP, et al. Among authors: kleczkowska a. Ann Genet. 1989;32(3):177-9. Ann Genet. 1989. PMID: 2486064

8

Normal phenotype and slight mental retardation in de novo distal 8p deletion (8pter----8p23.1:).

Fryns JP, Kleczkowska A, Vogels A, Van den Berghe H. Fryns JP, et al. Among authors: kleczkowska a. Ann Genet. 1989;32(3):171-3. Ann Genet. 1989. PMID: 2573313

9

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: kleczkowska a. Ann Genet. 1989;32(3):174-6. Ann Genet. 1989. PMID: 2573314

10

Interstitial deletion of the short arm of chromosome 4. A phenotype distinct from the Wolf-Hirschhorn syndrome.

Fryns JP, Yang-Aisheng, Kleczkowska A, Lemmens F, Vandecasseye W, van den Berghe H. Fryns JP, et al. Among authors: kleczkowska a. Ann Genet. 1989;32(1):59-61. Ann Genet. 1989. PMID: 2751251

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