Kleczkowska A - Search Results

1

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

2

On the excess of mental retardation and/or congenital malformations in apparently balanced reciprocal translocations. A critical review of the Leuven data 1966-1991.

Fryns JP, Kleczkowska A, Kubień E, Van Den Berghe H. Fryns JP, et al. Among authors: kleczkowska a. Genet Couns. 1991;2(4):185-94. Genet Couns. 1991. PMID: 1799415

3

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

4

Mosaic 46, XY/47,XY, + der(18)t(Y;18)(q11.22;q11.2) karyotype, moderate mental retardation and non-specific dysmorphism.

Fryns JP, Kleczkowska A, Van Den Berghe H. Fryns JP, et al. Among authors: kleczkowska a. Genet Couns. 1990;1(2):173-7. Genet Couns. 1990. PMID: 2081001 Review. No abstract available.

5

Cytogenetic findings in a consecutive series of 478 patients with Turner syndrome. The Leuven experience 1965-1989.

Kleczkowska A, Dmoch E, Kubien E, Fryns JP, Van den Berghe H. Kleczkowska A, et al. Genet Couns. 1990;1(3-4):227-33. Genet Couns. 1990. PMID: 2098046

6

Turner syndrome: the Leuven experience (1965-1989) in 478 patients. I. Patient's age at the time of diagnosis in relation to chromosomal findings.

Kleczkowska A, Kubien E, Fryns JP, Van den Berghe H. Kleczkowska A, et al. Genet Couns. 1990;1(3-4):235-40. Genet Couns. 1990. PMID: 2098047

7

Turner syndrome: II. Associated anomalies, mental performance and psychological problems in 218 patients diagnosed in Leuven in the period 1965-1989.

Kleczkowska A, Kubien E, Dmoch E, Fryns JP, Van den Berghe H. Kleczkowska A, et al. Genet Couns. 1990;1(3-4):241-9. Genet Couns. 1990. PMID: 2098048

8

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.

9

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.

10

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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

137 results

Search Page

Filters