Dereymaeker AM - Search Results

1

A peculiar subphenotype in the fra(X) syndrome: extreme obesity-short stature-stubby hands and feet-diffuse hyperpigmentation. Further evidence of disturbed hypothalamic function in the fra(X) syndrome?

Fryns JP, Haspeslagh M, Dereymaeker AM, Volcke P, Van den Berghe H. Fryns JP, et al. Among authors: dereymaeker am. Clin Genet. 1987 Dec;32(6):388-92. doi: 10.1111/j.1399-0004.1987.tb03155.x. Clin Genet. 1987. PMID: 3436088

2

Hypomelanosis of Ito and severe sensorineural deafness.

Fryns JP, Dereymaeker AM, Van Den Berghe H. Fryns JP, et al. Among authors: dereymaeker am. Genet Couns. 1992;3(3):149-51. Genet Couns. 1992. PMID: 1388933

3

On the etiology of hearing loss in a population of 155 institutionalized children.

Dereymaeker AM, Fryns JP, Ars B, Andrescescou J, Van den Berghe H. Dereymaeker AM, et al. Acta Otorhinolaryngol Belg. 1991;45(3):283-91. Acta Otorhinolaryngol Belg. 1991. PMID: 1659109

4

On the nosology of moderate mental retardation with special attention to X-linked mental retardation. A diagnostic genetic survey of 274 institutionalized moderately mentally retarded men.

Volcke P, Dereymaeker AM, Fryns JP, van den Berghe H. Volcke P, et al. Among authors: dereymaeker am. Genet Couns. 1990;1(1):47-56. Genet Couns. 1990. PMID: 2222922

5

EEC syndrome without ectrodactyly: report of two new families.

Fryns JP, Legius E, Dereymaeker AM, Van den Berghe H. Fryns JP, et al. Among authors: dereymaeker am. 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.

6

Retinitis pigmentosa, hearing loss and vitiligo: report of two patients.

Dereymaeker AM, Fryns JP, Ars J, Andresescu J, van den Berghe H. Dereymaeker AM, et al. Clin Genet. 1989 May;35(5):387-9. doi: 10.1111/j.1399-0004.1989.tb02959.x. Clin Genet. 1989. PMID: 2758690

7

A genetic-diagnostic survey in an institutionalized population of 158 mentally retarded patients. The Viaene experience.

Dereymaeker AM, Fryns JP, Haegeman J, Deroover J, Van den Berghe H. Dereymaeker AM, et al. Clin Genet. 1988 Aug;34(2):126-34. doi: 10.1111/j.1399-0004.1988.tb02848.x. Clin Genet. 1988. PMID: 2973379

8

Mental retardation and Y/8 translocation [karyotype: 46,XY, t(Y;8)(q12;q24)] in father and son.

Fryns JP, Kleczkowska A, Dereymaeker AM, Van den Berghe H. Fryns JP, et al. Among authors: dereymaeker am. Helv Paediatr Acta. 1988 Aug;43(1-2):87-90. Helv Paediatr Acta. 1988. PMID: 3170249

9

Oculocerebral syndrome with hypopigmentation (Cross syndrome). Report of two siblings born to consanguineous parents.

Fryns JP, Dereymaeker AM, Heremans G, Marien J, van Hauwaert J, Turner G, Hockey A, van den Berghe H. Fryns JP, et al. Among authors: dereymaeker am. Clin Genet. 1988 Aug;34(2):81-4. doi: 10.1111/j.1399-0004.1988.tb02840.x. Clin Genet. 1988. PMID: 3191612

10

Mental retardation, macrocephaly, short stature and craniofacial dysmorphism in three sisters. A new entity among the mental retardation-macrocephaly syndromes?

Fryns JP, Dereymaeker AM, Haegeman J, van den Berghe H. Fryns JP, et al. Among authors: dereymaeker am. Clin Genet. 1988 Apr;33(4):293-8. doi: 10.1111/j.1399-0004.1988.tb03451.x. Clin Genet. 1988. PMID: 3359686

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