Fryns JP - Search Results

1

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

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

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: fryns jp. Clin Genet. 1992 Jan;41(1):16-21. doi: 10.1111/j.1399-0004.1992.tb03621.x. Clin Genet. 1992. PMID: 1378778

3

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. Clin Genet. 1992 Dec;42(6):314-6. doi: 10.1111/j.1399-0004.1992.tb03263.x. Clin Genet. 1992. PMID: 1493644

4

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. 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

5

Cohen syndrome: fertility in a female patient.

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

6

A clinical, cytogenetic and familial study of 307 mentally retarded, institutionalized, adult male patients with special interest for fra(X) negative X-linked mental retardation.

Haspeslagh M, Fryns JP, Holvoet M, Collen G, Dierck G, Baeke J, van den Berghe H. Haspeslagh M, et al. Among authors: fryns jp. Clin Genet. 1991 Jun;39(6):434-41. doi: 10.1111/j.1399-0004.1991.tb03055.x. Clin Genet. 1991. PMID: 1863991

7

Mental retardation, craniofacial dysmorphism, hypogonadism, diabetes mellitus and epilepsy in four siblings. A "new" mental retardation syndrome.

Fryns JP, Vogels A, van den Berghe H. Fryns JP, et al. Clin Genet. 1990 Feb;37(2):111-6. doi: 10.1111/j.1399-0004.1990.tb03487.x. Clin Genet. 1990. PMID: 2107046

8

Cohen syndrome and de novo reciprocal translocation t(5;7)(q33.1;p15.1).

Fryns JP, Kleczkowska A, Smeets E, Thiry P, Geutjens J, Van den Berghe H. Fryns JP, et al. Am J Med Genet. 1990 Dec;37(4):546-7. doi: 10.1002/ajmg.1320370425. Am J Med Genet. 1990. PMID: 2260606

9

The female and the fragile X syndrome: data on clinical and psychological findings in 7 fra(X) carriers.

Borghgraef M, Fryns JP, van den Berghe H. Borghgraef M, et al. Among authors: fryns jp. Clin Genet. 1990 May;37(5):341-6. doi: 10.1111/j.1399-0004.1990.tb03516.x. Clin Genet. 1990. PMID: 2354547

10

Dominant branchial cleft syndrome with characteristics of both branchio-oto-renal and branchio-oculo-facial syndrome.

Legius E, Fryns JP, Van den Berghe H. Legius E, et al. Among authors: fryns jp. Clin Genet. 1990 May;37(5):347-50. doi: 10.1111/j.1399-0004.1990.tb03517.x. Clin Genet. 1990. PMID: 2354548

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