van den Berghe H - Search Results

1

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: van den berghe h. Ann Genet. 1989;32(1):59-61. Ann Genet. 1989. PMID: 2751251

2

Familial paracentric inversion of the short arm of chromosome 3.

Fryns JP, van den Berghe H. Fryns JP, et al. Among authors: van den berghe h. Ann Genet. 1979;22(3):163-4. Ann Genet. 1979. PMID: 316673

3

Trisomy of the short arm of chromosome 4: the changing phenotype with age.

Kleczkowska A, Fryns JP, van den Berghe H. Kleczkowska A, et al. Among authors: van den berghe h. Ann Genet. 1992;35(4):217-23. Ann Genet. 1992. PMID: 1296518 Review.

4

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: van den berghe h. Ann Genet. 1992;35(4):234-6. Ann Genet. 1992. PMID: 1296522

5

Rieger syndrome and interstitial 4q26 deletion.

Fryns JP, Van Den Berghe H. Fryns JP, et al. Among authors: van den berghe h. Genet Couns. 1992;3(3):153-4. Genet Couns. 1992. PMID: 1388934 No abstract available.

6

Transmission of ring chromosome 18 46,XX/46,XX,r(18) mosaicism in a mother and ring chromosome 18 syndrome in her son.

Fryns JP, Kleczkowska A, Smeets E, Van Den Berghe H. Fryns JP, et al. Among authors: van den berghe h. Ann Genet. 1992;35(2):121-3. Ann Genet. 1992. PMID: 1524410

7

Minimal dysmorphic stigmata in 9q deletion of paternal origin.

Kleczkowska A, Fryns JP, Lemli L, Van den Berghe H. Kleczkowska A, et al. Among authors: van den berghe h. Genet Couns. 1992;3(1):49-52. Genet Couns. 1992. PMID: 1590981

8

Prune-belly anomaly and large interstitial deletion of the long arm of chromosome 6.

Fryns JP, Vandenberghe K, Van den Berghe H. Fryns JP, et al. Among authors: van den berghe h. Ann Genet. 1991;34(2):127. Ann Genet. 1991. PMID: 1746884 No abstract available.

9

Cohen syndrome: fertility in a female patient.

Fryns JP, Lemmens F, van den Berghe H. Fryns JP, et al. Among authors: van den berghe h. Clin Genet. 1991 Dec;40(6):461-4. doi: 10.1111/j.1399-0004.1991.tb03118.x. Clin Genet. 1991. PMID: 1778007

10

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: van den berghe h. Genet Couns. 1991;2(2):109-13. Genet Couns. 1991. PMID: 1781954

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