Van den Berghe H - Search Results

1

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. Among authors: van den berghe h. Genet Couns. 1990;1(3-4):235-40. Genet Couns. 1990. PMID: 2098047

2

Hypomelanosis of Ito and severe sensorineural deafness.

Fryns JP, Dereymaeker AM, Van Den Berghe H. Fryns JP, et al. Among authors: van den berghe h. Genet Couns. 1992;3(3):149-51. Genet Couns. 1992. PMID: 1388933

3

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.

4

Pfeiffer acrocephalosyndactyly syndrome in mother and son with cloverleaf skull anomaly in the child.

Soekarman D, Fryns JP, van den Berghe H. Soekarman D, et al. Among authors: van den berghe h. Genet Couns. 1992;3(4):217-20. Genet Couns. 1992. PMID: 1472357

5

The cardio-facio-cutaneous (CFC) syndrome: autosomal dominant inheritance in a large family.

Fryns JP, Volcke P, Van den Berghe H. Fryns JP, et al. Among authors: van den berghe h. Genet Couns. 1992;3(1):19-24. Genet Couns. 1992. PMID: 1590976

6

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

7

Psychological profile and behavioural characteristics in 12 patients with Prader-Willi syndrome.

Borghgraef M, Fryns JP, Van Den Berghe H. Borghgraef M, et al. Among authors: van den berghe h. Genet Couns. 1990;1(2):141-50. Genet Couns. 1990. PMID: 1706926

8

Noonan phenotype in the basal cell nevus syndrome.

Grubben C, Fryns JP, Smeets E, Van den Berghe H. Grubben C, et al. Among authors: van den berghe h. Genet Couns. 1991;2(1):47-54. Genet Couns. 1991. PMID: 1741977

9

Role of gonadal dysgenesis in gonadoblastoma induction in 46, XY individuals. The Leuven experience in 46, XY pure gonadal dysgenesis and testicular feminization syndromes.

Lukusa T, Fryns JP, Kleczkowska A, Van den Berghe H. Lukusa T, et al. Among authors: van den berghe h. Genet Couns. 1991;2(1):9-16. Genet Couns. 1991. PMID: 1741980

10

The 48,XXYY syndrome. Follow-up data on clinical characteristics and psychological findings in 4 patients.

Borghgraef M, Fryns JP, Van den Berghe H. Borghgraef M, et al. Among authors: van den berghe h. Genet Couns. 1991;2(2):103-8. Genet Couns. 1991. PMID: 1781953

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