de Zegher F - Search Results

1

ARX mutation in a boy with transsphenoidal encephalocele and hypopituitarism.

Van Esch H, Poirier K, de Zegher F, Holvoet M, Bienvenu T, Chelly J, Devriendt K, Fryns JP. Van Esch H, et al. Among authors: de zegher f. Clin Genet. 2004 Jun;65(6):503-5. doi: 10.1111/j.1399-0004.2004.00256.x. Clin Genet. 2004. PMID: 15151512 No abstract available.

2

Anterior basal encephalocele in the median cleft face syndrome. Comments on nosology and treatment.

Grubben C, Fryns JP, De Zegher F, Van Den Berghe H. Grubben C, et al. Among authors: de zegher f. Genet Couns. 1990;1(2):103-9. Genet Couns. 1990. PMID: 2080994

3

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

4

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

5

Deletion of thyroid transcription factor-1 gene in an infant with neonatal thyroid dysfunction and respiratory failure.

Devriendt K, Vanhole C, Matthijs G, de Zegher F. Devriendt K, et al. Among authors: de zegher f. N Engl J Med. 1998 Apr 30;338(18):1317-8. doi: 10.1056/NEJM199804303381817. N Engl J Med. 1998. PMID: 9565498 No abstract available.

6

Duplication of the TGFBR1 gene causes features of Loeys-Dietz syndrome.

Breckpot J, Budts W, De Zegher F, Vermeesch JR, Devriendt K. Breckpot J, et al. Among authors: de zegher f. Eur J Med Genet. 2010 Nov-Dec;53(6):408-10. doi: 10.1016/j.ejmg.2010.08.004. Epub 2010 Sep 20. Eur J Med Genet. 2010. PMID: 20813212

7

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

8

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

9

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

10

Laryngeal atresia sequence as part of the DiGeorge developmental field defect.

Moerman P, de Zegher F, Vandenberghe K, Devlieger H, Petit P, Lauweryns JM, Fryns JP. Moerman P, et al. Among authors: de zegher f. Genet Couns. 1992;3(3):133-7. Genet Couns. 1992. PMID: 1388931

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