Kleczkowska A - Search Results

1

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

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

Apparent late-onset Cockayne syndrome and interstitial deletion of the long arm of chromosome 10 (del(10)(q11.23q21.2)).

Fryns JP, Bulcke J, Verdu P, Carton H, Kleczkowska A, Van den Berghe H. Fryns JP, et al. Among authors: kleczkowska a. Am J Med Genet. 1991 Sep 1;40(3):343-4. doi: 10.1002/ajmg.1320400320. Am J Med Genet. 1991. PMID: 1951442

4

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

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

6

On the variable effect of mosaic normal/balanced chromosomal rearrangements in man.

Kleczkowska A, Fryns JP, Van den Berghe H. Kleczkowska A, et al. J Med Genet. 1990 Aug;27(8):505-7. doi: 10.1136/jmg.27.8.505. J Med Genet. 1990. PMID: 2213843 Free PMC article.

7

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

8

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

9

On the familial occurrence of congenital bilateral absence of vas deferens.

Kleczkowska A, Fryns JP, Steeno O, van den Berghe H. Kleczkowska A, et al. Clin Genet. 1989 Apr;35(4):268-71. doi: 10.1111/j.1399-0004.1989.tb02941.x. Clin Genet. 1989. PMID: 2653673 Review.

10

De novo Robertsonian D/D type translocations: the Leuven experience.

Kleczkowska A, Fryns JP, Standaert L, van den Berghe H. Kleczkowska A, et al. Clin Genet. 1989 Jul;36(1):65-8. doi: 10.1111/j.1399-0004.1989.tb03368.x. Clin Genet. 1989. PMID: 2766564

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