de Zegher F - Search Results

1

Methylation defect in imprinted genes detected in patients with an Albright's hereditary osteodystrophy like phenotype and platelet Gs hypofunction.

Izzi B, Francois I, Labarque V, Thys C, Wittevrongel C, Devriendt K, Legius E, Van den Bruel A, D'Hooghe M, Lambrechts D, de Zegher F, Van Geet C, Freson K. Izzi B, et al. Among authors: de zegher f. PLoS One. 2012;7(6):e38579. doi: 10.1371/journal.pone.0038579. Epub 2012 Jun 5. PLoS One. 2012. PMID: 22679513 Free PMC article.

2

Opitz C syndrome and pseudohypoaldosteronism.

De Koster J, Legius E, de Zegher F, Devlieger H, Fryns JP, Eggermont E. De Koster J, et al. Among authors: de zegher f. Am J Med Genet. 1990 Dec;37(4):457-9. doi: 10.1002/ajmg.1320370405. Am J Med Genet. 1990. PMID: 2175542

3

Growth hormone deficiency and premature thelarche in a female infant with kabuki makeup syndrome.

Devriendt K, Lemli L, Craen M, de Zegher F. Devriendt K, et al. Among authors: de zegher f. Horm Res. 1995;43(6):303-6. doi: 10.1159/000184355. Horm Res. 1995. PMID: 7607617

4

Diaphragmatic hernia in Denys-Drash syndrome.

Devriendt K, Deloof E, Moerman P, Legius E, Vanhole C, de Zegher F, Proesmans W, Devlieger H. Devriendt K, et al. Among authors: de zegher f. Am J Med Genet. 1995 May 22;57(1):97-101. doi: 10.1002/ajmg.1320570120. Am J Med Genet. 1995. PMID: 7645607

5

Asplenia syndrome and isolated total anomalous pulmonary venous connection in siblings.

Devriendt K, Casaer A, Van Cauter A, de Zegher F, Dumoulin M, Gewillig M, Devlieger H. Devriendt K, et al. Among authors: de zegher f. Eur J Pediatr. 1994 Oct;153(10):712-4. doi: 10.1007/BF01954484. Eur J Pediatr. 1994. PMID: 7813525

6

[The dentofacial complex in hormonal treatment for growth retardation].

Van Erum R, Mulier MG, Carels C, François I, de Zegher F. Van Erum R, et al. Among authors: de zegher f. Rev Belge Med Dent (1984). 1994;49(4):18-25. Rev Belge Med Dent (1984). 1994. PMID: 7899617 French.

7

Opposite effects of growth hormone and estrogens on the pregnancy zone protein serum levels in children and adolescents.

Devriendt K, Massa G, de Zegher F, Vanderschueren-Lodeweyckx M, Cassiman JJ, Van den Berghe H, Marynen P. Devriendt K, et al. Among authors: de zegher f. Acta Endocrinol (Copenh). 1993 Apr;128(4):334-8. doi: 10.1530/acta.0.1280334. Acta Endocrinol (Copenh). 1993. PMID: 8498151

8

The foetal pituitary, postmaturity and breech presentation.

de Zegher F, Kaplan SL, Grumbach MM, Van den Berghe G, Francois I, Vanhole C, Devlieger H. de Zegher F, et al. Acta Paediatr. 1995 Oct;84(10):1100-2. doi: 10.1111/j.1651-2227.1995.tb13503.x. Acta Paediatr. 1995. PMID: 8563217 Review. No abstract available.

9

Paucity of intrahepatic bile ducts, solitary kidney and atrophic pancreas with diabetes mellitus: atypical Alagille syndrome?

Devriendt K, Dooms L, Proesmans W, de Zegher F, Desmet V, Eggermont E. Devriendt K, et al. Among authors: de zegher f. Eur J Pediatr. 1996 Feb;155(2):87-90. doi: 10.1007/BF02075756. Eur J Pediatr. 1996. PMID: 8775219

10

Association of hyperprolinaemia type I and heparin cofactor II deficiency with CATCH 22 syndrome: evidence for a contiguous gene syndrome locating the proline oxidase gene.

Jaeken J, Goemans N, Fryns JP, François I, de Zegher F. Jaeken J, et al. Among authors: de zegher f. J Inherit Metab Dis. 1996;19(3):275-7. doi: 10.1007/BF01799254. J Inherit Metab Dis. 1996. PMID: 8803768

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

403 results

Search Page

Filters