Fryns JP - Search Results

1

Submicroscopic deletion in chromosome 22q11 in trizygous triplet siblings and their father. Clinical variability of 22q11 deletion.

Devriendt K, Van Hoestenberghe R, Van Hole C, Devlieger H, Gewillig M, Moerman P, Van den Berghe H, Fryns JP. Devriendt K, et al. Among authors: fryns jp. Clin Genet. 1997 Apr;51(4):246-9. doi: 10.1111/j.1399-0004.1997.tb02463.x. Clin Genet. 1997. PMID: 9184246

2

Posterior scalp defects in Opitz syndrome. Another symptom related to a defect in midline development.

Fryns JP, Delooz J, van den Berghe H. Fryns JP, et al. Clin Genet. 1992 Dec;42(6):314-6. doi: 10.1111/j.1399-0004.1992.tb03263.x. Clin Genet. 1992. PMID: 1493644

3

Full 69,XXY triploidy and sex-reversal: a further example of true hermaphrodism associated with multiple malformations.

Petit P, Moerman P, Fryns JP. Petit P, et al. Among authors: fryns jp. Clin Genet. 1992 Apr;41(4):175-7. doi: 10.1111/j.1399-0004.1992.tb03658.x. Clin Genet. 1992. PMID: 1576753

4

Cohen syndrome: fertility in a female patient.

Fryns JP, Lemmens F, van den Berghe H. Fryns JP, et al. Clin Genet. 1991 Dec;40(6):461-4. doi: 10.1111/j.1399-0004.1991.tb03118.x. Clin Genet. 1991. PMID: 1778007

5

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

6

Dominant branchial cleft syndrome with characteristics of both branchio-oto-renal and branchio-oculo-facial syndrome.

Legius E, Fryns JP, Van den Berghe H. Legius E, et al. Among authors: fryns jp. Clin Genet. 1990 May;37(5):347-50. doi: 10.1111/j.1399-0004.1990.tb03517.x. Clin Genet. 1990. PMID: 2354548

7

An apparently new autosomal recessive syndrome with facial dysmorphism, macrocephaly, myopia and Dandy-Walker malformation.

Buttiens M, Fryns JP, van den Berghe H. Buttiens M, et al. Among authors: fryns jp. Clin Genet. 1989 Dec;36(6):451-55. doi: 10.1111/j.1399-0004.1989.tb03375.x. Clin Genet. 1989. PMID: 2591071

8

De novo Robertsonian D/D type translocations: the Leuven experience.

Kleczkowska A, Fryns JP, Standaert L, van den Berghe H. Kleczkowska A, et al. Among authors: fryns jp. Clin Genet. 1989 Jul;36(1):65-8. doi: 10.1111/j.1399-0004.1989.tb03368.x. Clin Genet. 1989. PMID: 2766564

9

Fertility and X-chromosome rearrangements: isodicentric X-chromosome formation in the mother and Xp deletion in her daughter.

Fryns JP, Kleczkowska A, Debucquoy P, van den Berghe H. Fryns JP, et al. Clin Genet. 1988 Nov;34(5):321-4. doi: 10.1111/j.1399-0004.1988.tb02885.x. Clin Genet. 1988. PMID: 3229000

10

De novo 3q/7q translocation and associated interstitial 7q35 deletion.

Fryns JP, Kleczkowska A, van den Berghe H. Fryns JP, et al. Clin Genet. 1988 Jan;33(1):60-2. doi: 10.1111/j.1399-0004.1988.tb04267.x. Clin Genet. 1988. PMID: 3342549

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

1,311 results

Search Page

Filters