Sidi D - Search Results

1

Upper limb malformations in DiGeorge syndrome.

Cormier-Daire V, Iserin L, Théophile D, Sidi D, Vervel C, Padovani JP, Vekemans M, Munnich A, Lyonnet S. Cormier-Daire V, et al. Among authors: sidi d. Am J Med Genet. 1995 Mar 13;56(1):39-41. doi: 10.1002/ajmg.1320560111. Am J Med Genet. 1995. PMID: 7747784

2

Microsatellite DNA markers detects 95% of chromosome 22q11 deletions.

Bonnet D, Cormier-Daire V, Kachaner J, Szezepanski I, Souillard P, Sidi D, Munnich A, Lyonnet S. Bonnet D, et al. Among authors: sidi d. Am J Med Genet. 1997 Jan 20;68(2):182-4. Am J Med Genet. 1997. PMID: 9028455

3

Ebstein anomaly associated with rearrangements of chromosomal region 11q.

de Lonlay-Debeney P, de Blois MC, Bonnet D, Amiel J, Abadie V, Picq M, Lyonnet S, Sidi D, Munnich A, Vekemans M, Cormier-Daire V. de Lonlay-Debeney P, et al. Among authors: sidi d. Am J Med Genet. 1998 Nov 2;80(2):157-9. doi: 10.1002/(sici)1096-8628(19981102)80:2<157::aid-ajmg12>3.0.co;2-u. Am J Med Genet. 1998. PMID: 9805133

4

Prevalence of the microdeletion 22q11 in newborn infants with congenital conotruncal cardiac anomalies.

Iserin L, de Lonlay P, Viot G, Sidi D, Kachaner J, Munnich A, Lyonnet S, Vekemans M, Bonnet D. Iserin L, et al. Among authors: sidi d. Eur J Pediatr. 1998 Nov;157(11):881-4. doi: 10.1007/s004310050959. Eur J Pediatr. 1998. PMID: 9835429

5

beta(1)-adrenergic antagonists improve sleep and behavioural disturbances in a circadian disorder, Smith-Magenis syndrome.

De Leersnyder H, de Blois MC, Vekemans M, Sidi D, Villain E, Kindermans C, Munnich A. De Leersnyder H, et al. Among authors: sidi d. J Med Genet. 2001 Sep;38(9):586-90. doi: 10.1136/jmg.38.9.586. J Med Genet. 2001. PMID: 11546826 Free PMC article.

6

Postnatal growth retardation, facial dysmorphism, spondylocarpal synostosis, cardiac defect, and inner ear malformation (cardiospondylocarpofacial syndrome?)--a distinct syndrome?

Sousa SB, Baujat G, Abadie V, Bonnet D, Sidi D, Munnich A, Krakow D, Cormier-Daire V. Sousa SB, et al. Among authors: sidi d. Am J Med Genet A. 2010 Mar;152A(3):539-46. doi: 10.1002/ajmg.a.33277. Am J Med Genet A. 2010. PMID: 20186786

7

Relation of genotype 22q11 deletion to phenotype of pulmonary vessels in tetralogy of Fallot and pulmonary atresia-ventricular septal defect.

Chessa M, Butera G, Bonhoeffer P, Iserin L, Kachaner J, Lyonnet S, Munnich A, Sidi D, Bonnet D. Chessa M, et al. Among authors: sidi d. Heart. 1998 Feb;79(2):186-90. doi: 10.1136/hrt.79.2.186. Heart. 1998. PMID: 9538314 Free PMC article.

8

Tricuspid atresia and conotruncal malformations in five families.

Bonnet D, Fermont L, Kachaner J, Sidi D, Amiel J, Lyonnet S, Munnich A. Bonnet D, et al. Among authors: sidi d. J Med Genet. 1999 Apr;36(4):349-50. J Med Genet. 1999. PMID: 10227411 Free PMC article. No abstract available.

9

Prevalence of 22q11 deletion in fetuses with conotruncal cardiac defects: a 6-year prospective study.

Boudjemline Y, Fermont L, Le Bidois J, Lyonnet S, Sidi D, Bonnet D. Boudjemline Y, et al. Among authors: sidi d. J Pediatr. 2001 Apr;138(4):520-4. doi: 10.1067/mpd.2001.112174. J Pediatr. 2001. PMID: 11295715

10

Skin elastic fibers in Williams syndrome.

Dridi SM, Ghomrasseni S, Bonnet D, Aggoun Y, Vabres P, Bodemer C, Lyonnet S, de Prost Y, Fraitag S, Pellat B, Sidi D, Godeau G. Dridi SM, et al. Among authors: sidi d. Am J Med Genet. 1999 Nov 19;87(2):134-8. Am J Med Genet. 1999. PMID: 10533027

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