Sidi D - Search Results

1

A gene for Holt-Oram syndrome maps to the distal long arm of chromosome 12.

Bonnet D, Pelet A, Legeai-Mallet L, Sidi D, Mathieu M, Parent P, Plauchu H, Serville F, Schinzel A, Weissenbach J, et al. Bonnet D, et al. Among authors: sidi d. Nat Genet. 1994 Apr;6(4):405-8. doi: 10.1038/ng0494-405. Nat Genet. 1994. PMID: 8054983

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

[What's new in pediatric cardiology?].

Bonnet D, Sidi D. Bonnet D, et al. Among authors: sidi d. Arch Pediatr. 1999 Jul;6(7):777-80. doi: 10.1016/s0929-693x(99)80364-9. Arch Pediatr. 1999. PMID: 10429822 Review. French.

5

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

6

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

7

Prenatal detection of a tetralogy of Fallot with origin of the left pulmonary artery from the ascending aorta in a familial 22q11 microdeletion.

Saliba Z, Le Bidois J, Sidi D, Kachaner J, Bonnet D. Saliba Z, et al. Among authors: sidi d. Prenat Diagn. 1999 Mar;19(3):260-2. doi: 10.1002/(sici)1097-0223(199903)19:3<260::aid-pd522>3.0.co;2-d. Prenat Diagn. 1999. PMID: 10210126

8

[Pseudo-inherited form of left heart obstructive defects revealing maternal phenylketonuria].

Saliba Z, Bah G, Martin D, Abadie V, Azar Z, Fraisse A, Sidi D, Kachaner J, Bonnet D. Saliba Z, et al. Among authors: sidi d. Arch Mal Coeur Vaiss. 2000 May;93(5):649-52. Arch Mal Coeur Vaiss. 2000. PMID: 10858866 French.

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

[Prenatal diagnosis of conotruncal heart diseases. Results in 337 cases].

Boudjemline Y, Fermont L, Le Bidois J, Fraisse A, Kachaner J, Villain E, Sidi D, Bonnet D. Boudjemline Y, et al. Among authors: sidi d. Arch Mal Coeur Vaiss. 2000 May;93(5):583-6. Arch Mal Coeur Vaiss. 2000. PMID: 10858856 French.

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