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	1.	[The neurofibromatosis-Noonan syndrome: 4 cases]. [electronic resource] by Bouloc, A Lemerrer, M Blanchet-Bardon, C Producer: 19940713 In: Annales de dermatologie et de venereologie vol. 120 Availability: No items available. Save to lists Add to cart (remove)
	2.	Idiopathic thrombocytopenic purpura in two mothers of children with DiGeorge sequence: a new component manifestation of deletion 22q11? [electronic resource] by Lévy, A Michel, G Lemerrer, M Philip, N Producer: 19970714 In: American journal of medical genetics vol. 69 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	SHORT syndrome: a case with high hyperopia and astigmatism. [electronic resource] by Bonnel, S Dureau, P LeMerrer, M Dufier, J L Producer: 20010208 In: Ophthalmic genetics vol. 21 Availability: No items available. Save to lists Add to cart (remove)
	4.	[Congenital or neonatal hypothyroidism with filter-paper levels of TSH less than 50 microU/ml. Conclusions on the detection strategy in France]. [electronic resource] by Léger, J Lemerrer, M Briard, M L Czernichow, P Producer: 19870428 In: Archives francaises de pediatrie vol. 44 Availability: No items available. Save to lists Add to cart (remove)
	5.	Hypothyroidism in children with filter paper TSH of 30 to 50 microU/ml at initial screening. Implication of the TSH cut-off point for recalling of infants at risk. [electronic resource] by Leger, J Lemerrer, M Briard, M L Czernichow, P Producer: 19871015 In: Acta paediatrica Scandinavica vol. 76 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Prenatal diagnosis of cleft lip at 11 menstrual weeks using embryoscopy in the van der Woude syndrome. [electronic resource] by Dommergues, M Lemerrer, M Couly, G Delezoide, A L Dumez, Y Producer: 19950818 In: Prenatal diagnosis vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Can Hutchinson-Gilford progeria syndrome be a neonatal condition? [electronic resource] by Faivre, L Khau Van Kien, P Madinier-Chappat, N Nivelon-Chevallier, A Beer, F LeMerrer, M Producer: 20000309 In: American journal of medical genetics vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Meckel-Gruber syndrome: prenatal diagnosis at 10 menstrual weeks using embryoscopy. [electronic resource] by Dumez, Y Dommergues, M Gubler, M C Bunduki, V Narcy, F LeMerrer, M Mandelbrot, L Berkowitz, R Producer: 19940616 In: Prenatal diagnosis vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Prenatal diagnosis of sporadic Apert syndrome: a sequential diagnostic approach combining three-dimensional computed tomography and molecular biology. [electronic resource] by Mahieu-Caputo, D Sonigo, P Amiel, J Simon, I Aubry, M C Lemerrer, M Delezoïde, A L Gigarel, N Dommergues, M Dumez, Y Producer: 20010208 In: Fetal diagnosis and therapy vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Mazabraud syndrome in two patients: clinical overlap with McCune-Albright syndrome. [electronic resource] by Faivre, L Nivelon-Chevallier, A Kottler, M L Robinet, C Khau Van Kien, P Lorcerie, B Munnich, A Maroteaux, P Cormier-Daire, V LeMerrer, M Producer: 20010607 In: American journal of medical genetics vol. 99 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Fibrodysplasia ossificans progressiva, a heritable disorder of severe heterotopic ossification, maps to human chromosome 4q27-31. [electronic resource] by Feldman, G Li, M Martin, S Urbanek, M Urtizberea, J A Fardeau, M LeMerrer, M Connor, J M Triffitt, J Smith, R Muenke, M Kaplan, F S Shore, E M Producer: 20000309 In: American journal of human genetics vol. 66 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	CHARGE syndrome: report of 47 cases and review. [electronic resource] by Tellier, A L Cormier-Daire, V Abadie, V Amiel, J Sigaudy, S Bonnet, D de Lonlay-Debeney, P Morrisseau-Durand, M P Hubert, P Michel, J L Jan, D Dollfus, H Baumann, C Labrune, P Lacombe, D Philip, N LeMerrer, M Briard, M L Munnich, A Lyonnet, S Producer: 19980811 In: American journal of medical genetics vol. 76 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)