Delooz J - Search Results

Save citations to file

Email citations

Your saved search

Your RSS Feed

Page 1

Turner syndrome patients as adults: a study of their cognitive profile, psychosocial functioning and psychopathological findings.

Delooz J, Van den Berghe H, Swillen A, Kleczkowska A, Fryns JP. Delooz J, et al. Genet Couns. 1993;4(3):169-79. Genet Couns. 1993. PMID: 8267923

Tetraphocomelia and bilateral femorotibial synostosis. A severe variant of the thrombocytopenia-absent radii (TAR) syndrome?

Delooz J, Moerman P, Van den Berghe K, Fryns JP. Delooz J, et al. Genet Couns. 1992;3(2):91-3. Genet Couns. 1992. PMID: 1642816

Unknown syndrome: nasal hypoplasia, sparse hair, truncal obesity, genital hypoplasia, and severe mental retardation.

Fryns JP, Delooz J, Van Den Berghe H. Fryns JP, et al. Among authors: delooz j. J Med Genet. 1992 Sep;29(9):676-7. doi: 10.1136/jmg.29.9.676. J Med Genet. 1992. PMID: 1404303 Free PMC article.

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. Among authors: delooz j. Clin Genet. 1992 Dec;42(6):314-6. doi: 10.1111/j.1399-0004.1992.tb03263.x. Clin Genet. 1992. PMID: 1493644

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

4 results

Search Page

Filters