Kachaner J - Search Results

1

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: kachaner j. Am J Med Genet. 1997 Jan 20;68(2):182-4. Am J Med Genet. 1997. PMID: 9028455

2

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: kachaner j. Eur J Pediatr. 1998 Nov;157(11):881-4. doi: 10.1007/s004310050959. Eur J Pediatr. 1998. PMID: 9835429

3

No evidence for linkage to the type 1 or type 2 neurofibromatosis loci in Noonan syndrome families.

Flintoff WF, Bahuau M, Lyonnet S, Gilgenkrantz S, Lacombe D, Marçon F, Levilliers J, Kachaner J, Munnich A, Le Merrer M. Flintoff WF, et al. Among authors: kachaner j. Am J Med Genet. 1993 Jul 1;46(6):700-5. doi: 10.1002/ajmg.1320460621. Am J Med Genet. 1993. PMID: 8362913

4

[Gene localisation in 12q12 in Holt-Oram atrio-digital syndrome].

Bonnet D, Terrett J, Pequignot-Viegas E, Weissenbach J, Munnich A, Lyonnet S, Kachaner J. Bonnet D, et al. Among authors: kachaner j. Arch Mal Coeur Vaiss. 1995 May;88(5):661-6. Arch Mal Coeur Vaiss. 1995. PMID: 7646274 Review. French.

5

The multi-track angiography catheter: a new tool for complex catheterisation in congenital heart disease.

Bonhoeffer P, Piéchaud JF, Stümper O, Bonnet D, Aggoun Y, Sidi D, Kachaner J. Bonhoeffer P, et al. Among authors: kachaner j. Heart. 1996 Aug;76(2):173-7. doi: 10.1136/hrt.76.2.173. Heart. 1996. PMID: 8795483 Free PMC article.

6

Atrio-ventricular valve dysplasia in 22 newborn infants.

Bonnet D, Saygili A, Bonhoeffer P, Fermont L, Sidi D, Kachaner J. Bonnet D, et al. Among authors: kachaner j. Int J Cardiol. 1997 Apr 18;59(2):113-8. doi: 10.1016/s0167-5273(97)02937-9. Int J Cardiol. 1997. PMID: 9158161

7

[Congenital coronary-cardiac fistula in children. Effects of surgical occlusion and percutaneous embolization].

Aggoun Y, Bonhoeffer P, Sidi D, Bonnet D, Acar P, Kachaner J. Aggoun Y, et al. Among authors: kachaner j. Arch Mal Coeur Vaiss. 1997 May;90(5):605-9. Arch Mal Coeur Vaiss. 1997. PMID: 9295939 French.

8

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: kachaner j. Heart. 1998 Feb;79(2):186-90. doi: 10.1136/hrt.79.2.186. Heart. 1998. PMID: 9538314 Free PMC article.

9

[A pulmonary vascularization study in pulmonary atresia with an interventricular defect in relation to the presence of a chromosome 22 deletion].

Chessa M, Bonhoeffer P, Butera G, Aggoun Y, Iserin L, Kachaner J, Sidi D, Bonnet D. Chessa M, et al. Among authors: kachaner j. G Ital Cardiol. 1998 Jun;28(6):661-5. G Ital Cardiol. 1998. PMID: 9672779 Italian.

10

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: kachaner j. 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

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