Van den Berghe H - Search Results

1

On the etiology of hearing loss in a population of 155 institutionalized children.

Dereymaeker AM, Fryns JP, Ars B, Andrescescou J, Van den Berghe H. Dereymaeker AM, et al. Among authors: van den berghe h. Acta Otorhinolaryngol Belg. 1991;45(3):283-91. Acta Otorhinolaryngol Belg. 1991. PMID: 1659109

2

Retinitis pigmentosa, hearing loss and vitiligo: report of two patients.

Dereymaeker AM, Fryns JP, Ars J, Andresescu J, van den Berghe H. Dereymaeker AM, et al. Among authors: van den berghe h. Clin Genet. 1989 May;35(5):387-9. doi: 10.1111/j.1399-0004.1989.tb02959.x. Clin Genet. 1989. PMID: 2758690

3

A genetic-diagnostic survey in an institutionalized population of 158 mentally retarded patients. The Viaene experience.

Dereymaeker AM, Fryns JP, Haegeman J, Deroover J, Van den Berghe H. Dereymaeker AM, et al. Among authors: van den berghe h. Clin Genet. 1988 Aug;34(2):126-34. doi: 10.1111/j.1399-0004.1988.tb02848.x. Clin Genet. 1988. PMID: 2973379

4

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

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

Occipital scalp defect associated with valvular pulmonary stenosis. A new entity?

Fryns JP, de Cock P, van den Berghe H. Fryns JP, et al. Among authors: van den berghe h. Clin Genet. 1992 Aug;42(2):97-9. doi: 10.1111/j.1399-0004.1992.tb03147.x. Clin Genet. 1992. PMID: 1424238

7

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

8

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

9

Hallermann-Streiff syndrome: clinical and psychological findings in children. Nosologic overlap with oculodentodigital dysplasia?

Spaepen A, Schrander-Stumpel C, Fryns JP, de Die-Smulders C, Borghgraef M, Van den Berghe H. Spaepen A, et al. Among authors: van den berghe h. Am J Med Genet. 1991 Dec 15;41(4):517-20. doi: 10.1002/ajmg.1320410428. Am J Med Genet. 1991. PMID: 1663704

10

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

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