Van den Berghe H - Search Results

1

Ichthyosis-characteristic appearance-mental retardation syndrome with distinct histological skin abnormalities.

Devriendt K, van den Oord J, De Vos R, Van den Berghe H, Fryns JP. Devriendt K, et al. Among authors: van den oord j, van den berghe h. Am J Med Genet. 1996 Jan 11;61(2):127-30. doi: 10.1002/(SICI)1096-8628(19960111)61:2<127::AID-AJMG4>3.0.CO;2-U. Am J Med Genet. 1996. PMID: 8669437

2

Severe pre- and postnatal growth retardation, developmental delay with hypotonia and marked hypotrophy of the distal extremities, dental anomalies, and eczematous skin. A new autosomal recessive entity.

Grubben C, de Cock P, Borghgraef M, van den Berghe H, Fryns JP. Grubben C, et al. Among authors: van den berghe h. Clin Genet. 1992 Jan;41(1):16-21. doi: 10.1111/j.1399-0004.1992.tb03621.x. Clin Genet. 1992. PMID: 1378778

3

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

4

Unknown syndrome: nasal hypoplasia, sparse hair, truncal obesity, genital hypoplasia, and severe mental retardation.

Fryns JP, Delooz J, Van Den Berghe H. Fryns JP, et al. Among authors: van den berghe h. J Med Genet. 1992 Sep;29(9):676-7. doi: 10.1136/jmg.29.9.676. J Med Genet. 1992. PMID: 1404303 Free PMC article.

5

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

6

Posterior scalp defects in Opitz syndrome. Another symptom related to a defect in midline development.

Fryns JP, Delooz J, van den Berghe H. Fryns JP, et al. Among authors: van den berghe h. Clin Genet. 1992 Dec;42(6):314-6. doi: 10.1111/j.1399-0004.1992.tb03263.x. Clin Genet. 1992. PMID: 1493644

7

MASA syndrome: delineation of the clinical spectrum at prepubertal age.

Fryns JP, Schrander-Stumpel C, De Die-Smulders C, Borghgraef M, Van den Berghe H. Fryns JP, et al. Among authors: van den berghe h. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):402-7. doi: 10.1002/ajmg.1320430161. Am J Med Genet. 1992. PMID: 1605218

8

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

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

X-linked mental retardation with Marfanoid habitus: a changing phenotype with age?

Fryns JP, Van Den Berghe H. Fryns JP, et al. Among authors: van den berghe h. Genet Couns. 1991;2(4):241-4. Genet Couns. 1991. PMID: 1799424

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