Fryns JP - Search Results

1

Anodontia as the sole clinical sign of the ectrodactyly-ectodermal dysplasia-cleft lip (EEC) syndrome.

Chranowska KH, Krajewska-Walasek M, Rump Z, Wisniewski L, Fryns JP. Chranowska KH, et al. Among authors: fryns jp. Genet Couns. 1990;1(1):67-73. Genet Couns. 1990. PMID: 2222925

2

Phenotype variability in the Miller acrofacial dysostosis syndrome. Report of two further patients.

Chrzanowska KH, Fryns JP, Krajewska-Walasek M, Wisniewski L, Van den Berghe H. Chrzanowska KH, et al. Among authors: fryns jp. Clin Genet. 1989 Feb;35(2):157-60. doi: 10.1111/j.1399-0004.1989.tb02922.x. Clin Genet. 1989. PMID: 2721025

3

Skeletal dysplasia syndrome with progeroid appearance, characteristic facial and limb anomalies, multiple synostoses, and distinct skeletal changes: a variant example of the Lenz-Majewski syndrome.

Chrzanowska KH, Fryns JP, Krajewska-Walasek M, Van den Berghe H, Wisniewski L. Chrzanowska KH, et al. Among authors: fryns jp. Am J Med Genet. 1989 Apr;32(4):470-4. doi: 10.1002/ajmg.1320320407. Am J Med Genet. 1989. PMID: 2773987

4

Increased head circumference and facial cleft as presenting signs of the nevoid basal-cell carcinoma syndrome.

Soekarman D, Fryns JP, Casaer P, Van Den Berghe H. Soekarman D, et al. Among authors: fryns jp. Genet Couns. 1991;2(3):157-62. Genet Couns. 1991. PMID: 1801852

5

Anterior basal encephalocele in the median cleft face syndrome. Comments on nosology and treatment.

Grubben C, Fryns JP, De Zegher F, Van Den Berghe H. Grubben C, et al. Among authors: fryns jp. Genet Couns. 1990;1(2):103-9. Genet Couns. 1990. PMID: 2080994

6

EEC syndrome without ectrodactyly: report of two new families.

Fryns JP, Legius E, Dereymaeker AM, Van den Berghe H. Fryns JP, et al. J Med Genet. 1990 Mar;27(3):165-8. doi: 10.1136/jmg.27.3.165. J Med Genet. 1990. PMID: 2325090 Free PMC article.

7

Thrombocytopenia and cleft hand in monosomy 21.

Vogels A, de Smet L, van den Berghe H, Fryns JP. Vogels A, et al. Among authors: fryns jp. Genet Couns. 1994;5(1):67-71. Genet Couns. 1994. PMID: 8031538

8

Intrafamilial clinical variability in type C brachydactyly.

Debeer P, De Smet L, Fryns JP. Debeer P, et al. Among authors: fryns jp. Genet Couns. 2001;12(4):353-8. Genet Couns. 2001. PMID: 11837604

9

DiGeorge syndrome and unilateral symbrachydactyly.

Devriendt K, De Smet L, De Boeck K, Fryns JP. Devriendt K, et al. Among authors: fryns jp. Genet Couns. 1997;8(4):345-7. Genet Couns. 1997. PMID: 9457506

10

The concurrence of ring constrictions in Adams-Oliver syndrome: additional evidence for vascular disruption as common pathogenetic mechanism.

Keymolen K, De Smet L, Bracke P, Fryns JP. Keymolen K, et al. Among authors: fryns jp. Genet Couns. 1999;10(3):295-300. Genet Couns. 1999. PMID: 10546102

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