Van den Berghe H - Search Results

1

Acrocentric/18p translocation in two mentally retarded males. Delineation of the adult phenotype.

Fryns JP, Kleczkowska A, Vinken L, Geutjens J, Smeets E, Van den Berghe H. Fryns JP, et al. Among authors: van den berghe h. Ann Genet. 1986;29(2):107-11. Ann Genet. 1986. PMID: 3490204

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

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: van den berghe h. Ann Genet. 1989;32(3):171-3. Ann Genet. 1989. PMID: 2573313

6

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: van den berghe h. Ann Genet. 1989;32(3):174-6. Ann Genet. 1989. PMID: 2573314

7

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

8

Severe midline fusion defects in a newborn with 10q26----qter deletion.

Fryns JP, Kleczkowska A, Fivez H, Van den Berghe H. Fryns JP, et al. Among authors: van den berghe h. Ann Genet. 1989;32(2):124-5. Ann Genet. 1989. PMID: 2757362

9

Ring chromosome 4 mosaicism and Potter sequence.

Fryns JP, Kleczkowska A, Jaeken J, Van den Berghe H. Fryns JP, et al. Among authors: van den berghe h. Ann Genet. 1988;31(2):120-2. Ann Genet. 1988. PMID: 3261147

10

The fetal phenotype in 15q2 duplication.

Fryns JP, Kleczkowska A, Moerman P, Vandenberghe K, Van den Berghe H. Fryns JP, et al. Among authors: van den berghe h. Ann Genet. 1988;31(2):123-5. Ann Genet. 1988. PMID: 3261148

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