Vogels A - Search Results

1

Presenting symptoms and clinical features in 130 patients with the velo-cardio-facial syndrome. The Leuven experience.

Vantrappen G, Devriendt K, Swillen A, Rommel N, Vogels A, Eyskens B, Gewillig M, Feenstra L, Fryns JP. Vantrappen G, et al. Among authors: vogels a. Genet Couns. 1999;10(1):3-9. Genet Couns. 1999. PMID: 10191424 Review.

2

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. Among authors: vogels a. Clin Genet. 1990 Feb;37(2):111-6. doi: 10.1111/j.1399-0004.1990.tb03487.x. Clin Genet. 1990. PMID: 2107046

3

Craniosynostosis and low middle frequency perceptive deafness in mother and son. A distinct entity?

Fryns JP, Vogels A, van den Berghe H. Fryns JP, et al. Among authors: vogels a. Genet Couns. 1990;1(1):63-6. Genet Couns. 1990. PMID: 2222924

4

Normal phenotype and slight mental retardation in de novo distal 8p deletion (8pter----8p23.1:).

Fryns JP, Kleczkowska A, Vogels A, Van den Berghe H. Fryns JP, et al. Among authors: vogels a. Ann Genet. 1989;32(3):171-3. Ann Genet. 1989. PMID: 2573313

5

Variable expression of the popliteal pterygium syndrome in two 3-generation families.

Soekarman D, Cobben JM, Vogels A, Spauwen PH, Fryns JP. Soekarman D, et al. Among authors: vogels a. Clin Genet. 1995 Apr;47(4):169-74. doi: 10.1111/j.1399-0004.1995.tb03954.x. Clin Genet. 1995. PMID: 7628117

6

Costello syndrome: a postnatal growth retardation syndrome with distinct phenotype.

Fryns JP, Vogels A, Haegeman J, Eggermont E, van den Berghe H. Fryns JP, et al. Among authors: vogels a. Genet Couns. 1994;5(4):337-43. Genet Couns. 1994. PMID: 7888135

7

Thrombocytopenia and cleft hand in monosomy 21.

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

8

The hand-foot-genital syndrome: on the variable expression in affected males.

Fryns JP, Vogels A, Decock P, van den Berghe H. Fryns JP, et al. Among authors: vogels a. Clin Genet. 1993 May;43(5):232-4. doi: 10.1111/j.1399-0004.1993.tb03808.x. Clin Genet. 1993. PMID: 8375102

9

Facial asymmetry, cardio-vascular anomalies and adducted thumbs as unusual symptoms in Dubowitz syndrome?

Vogels A, Lorenzetti ME, Gillis P, Fryns JP. Vogels A, et al. Ann Genet. 1996;39(1):31-4. Ann Genet. 1996. PMID: 9297441 Review.

10

Pierre-Robin sequence and severe mental retardation with chaotic behaviour associated with a small interstitial deletion in the long arm of chromosome 2 (del(2)(q331q333)).

Vogels A, Haegeman J, Fryns JP. Vogels A, et al. Genet Couns. 1997;8(3):249-52. Genet Couns. 1997. PMID: 9327270

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