Borghgraef M - Search Results

1

Psychological profile and behavioural characteristics in 12 patients with Prader-Willi syndrome.

Borghgraef M, Fryns JP, Van Den Berghe H. Borghgraef M, et al. Genet Couns. 1990;1(2):141-50. Genet Couns. 1990. PMID: 1706926

2

Von Recklinghausen-neurofibromatosis: a study of the psychological profile.

Spaepen A, Borghgraef M, Fryns JP. Spaepen A, et al. Among authors: borghgraef m. Birth Defects Orig Artic Ser. 1992;28(1):85-91. Birth Defects Orig Artic Ser. 1992. PMID: 1340240 No abstract available.

3

The 48,XXYY syndrome. Follow-up data on clinical characteristics and psychological findings in 4 patients.

Borghgraef M, Fryns JP, Van den Berghe H. Borghgraef M, et al. Genet Couns. 1991;2(2):103-8. Genet Couns. 1991. PMID: 1781953

4

Ring chromosome 15: follow-up data on physical and psychological development.

Fryns JP, Borghgraef M, Kleczkowska A, Van Den Berghe H. Fryns JP, et al. Among authors: borghgraef m. Genet Couns. 1990;1(2):167-72. Genet Couns. 1990. PMID: 2081000

5

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. Clin Genet. 1990 May;37(5):341-6. doi: 10.1111/j.1399-0004.1990.tb03516.x. Clin Genet. 1990. PMID: 2354547

6

Psychological findings in three children with ring 15 chromosome.

Borghgraef M, Fryns JP, Van den Berghe H. Borghgraef M, et al. J Ment Defic Res. 1988 Aug;32 ( Pt 4):337-47. doi: 10.1111/j.1365-2788.1988.tb01422.x. J Ment Defic Res. 1988. PMID: 3063822 Review.

7

The 49,XXXXY syndrome. Clinical and psychological follow-up data.

Borghgraef M, Fryns JP, Smeets E, Marien J, van Den Berghe H. Borghgraef M, et al. Clin Genet. 1988 Jun;33(6):429-34. doi: 10.1111/j.1399-0004.1988.tb03476.x. Clin Genet. 1988. PMID: 3168316

8

Fragile X boys: evolution of the mental age in childhood. Preliminary data on 10 prepubertal boys.

Borghgraef M, Swillen A, Van den Berghe H, Fryns JP. Borghgraef M, et al. Genet Couns. 1995;6(2):97-101. Genet Couns. 1995. PMID: 7546457

9

Terminal deletion of long arm of chromosome 4: patient report and literature review.

Evers LJ, Schrander-Stumpel CT, Engelen JJ, Mulder H, Borghgraef M, Fryns JP. Evers LJ, et al. Among authors: borghgraef m. Genet Couns. 1993;4(2):139-45. Genet Couns. 1993. PMID: 7689326 Review.

10

Adults with Williams-Beuren syndrome: evaluation of the medical, psychological and behavioral aspects.

Plissart L, Borghgraef M, Volcke P, Van den Berghe H, Fryns JP. Plissart L, et al. Among authors: borghgraef m. Clin Genet. 1994 Aug;46(2):161-7. doi: 10.1111/j.1399-0004.1994.tb04218.x. Clin Genet. 1994. PMID: 7820925

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

51 results

Search Page

Filters