Fryns JP - Search Results

1

The Coffin-Lowry syndrome. A study of two new index patients and their families.

Haspeslagh M, Fryns JP, Beusen L, Van Dessel F, Vinken L, Moens E, Van den Berghe H. Haspeslagh M, et al. Among authors: fryns jp. Eur J Pediatr. 1984 Dec;143(2):82-6. doi: 10.1007/BF00445790. Eur J Pediatr. 1984. PMID: 6519116

2

Corneal clouding, subvalvular aortic stenosis, and midfacial hypoplasia associated with mental deficiency and growth retardation--a new syndrome?

Fryns JP, Van den Berghe H. Fryns JP, et al. Eur J Pediatr. 1979 Jun 28;131(3):179-83. doi: 10.1007/BF00538941. Eur J Pediatr. 1979. PMID: 573203

3

The Greig polysyndactyly-craniofacial dysmorphism syndrome.

Fryns JP, Coeck W, van den Berghe H. Fryns JP, et al. Eur J Pediatr. 1977 Nov 4;126(4):283-7. doi: 10.1007/BF00477055. Eur J Pediatr. 1977. PMID: 201464

4

18q- syndrome in mother and daughter.

Fryns JP, Logghe N, van Eygen M, van den Berghe H. Fryns JP, et al. Eur J Pediatr. 1979 Mar 1;130(3):189-92. doi: 10.1007/BF00455265. Eur J Pediatr. 1979. PMID: 421697

5

The Coffin syndrome.

Fryns JP, Vinken L, Van den Berghe H. Fryns JP, et al. Hum Genet. 1977 May 10;36(3):271-6. doi: 10.1007/BF00446276. Hum Genet. 1977. PMID: 852873

6

A genetic diagnostic survey in an institutionalized population of 262 moderately mentally retarded patients: the Borgerstein experience.

Fryns JP, Volcke PH, Haspeslagh M, Beusen L, Van den Berghe H. Fryns JP, et al. J Ment Defic Res. 1990 Feb;34 ( Pt 1):29-40. doi: 10.1111/j.1365-2788.1990.tb01512.x. J Ment Defic Res. 1990. PMID: 2325119

7

On the occurrence of macroorchidism and mental handicap in the Aarskog syndrome.

Fryns JP, Van den Berghe H. Fryns JP, et al. J Genet Hum. 1989 Sep;37(3):221-3. J Genet Hum. 1989. PMID: 2625624

8

Facial paralysis at the age of 2 months as a first clinical sign of van Buchem disease (endosteal hyperostosis).

Fryns JP, Van den Berghe H. Fryns JP, et al. Eur J Pediatr. 1988 Jan;147(1):99-100. doi: 10.1007/BF00442624. Eur J Pediatr. 1988. PMID: 3276528

9

Multiple pterygium syndrome type Escobar in two brothers. Follow-up data from childhood to adulthood.

Fryns JP, Volcke P, van den Berghe H. Fryns JP, et al. Eur J Pediatr. 1988 Jun;147(5):550-2. doi: 10.1007/BF00441989. Eur J Pediatr. 1988. PMID: 3409934

10

Aniridia-Wilms' tumor association and 11p interstitial deletion.

Fryns JP, Beirinckx J, De Sutter E, Derluyn J, Francois J, Van den Berghe H. Fryns JP, et al. Eur J Pediatr. 1981 Mar;136(1):91-2. doi: 10.1007/BF00441718. Eur J Pediatr. 1981. PMID: 6260504

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