Your search returned 34 results.

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	1.	[Concern with systematic registration of medical data]. [electronic resource] by Ayme, S Addor, M C Producer: 20001128 In: Schweizerische medizinische Wochenschrift vol. 130 Availability: No items available. Save to lists Add to cart (remove)
	2.	[Trisomy 21 and its prenatal detection in the Canton of Vaud (1980-1996)]. [electronic resource] by Pescia, G Addor, M C Producer: 20001128 In: Schweizerische medizinische Wochenschrift vol. 130 Availability: No items available. Save to lists Add to cart (remove)
	3.	[The abnormal child: several definitions]. [electronic resource] by Addor, M C Schorderet, D F Producer: 20000912 In: Revue medicale de la Suisse romande vol. 120 Availability: No items available. Save to lists Add to cart (remove)
	4.	[Data on selected prenatal malformations in the EUROCAT study. Results of Zurich Canton from 1988 to 1997]. [electronic resource] by Achermann, S Addor, M C Schinzel, A Producer: 20001128 In: Schweizerische medizinische Wochenschrift vol. 130 Availability: No items available. Save to lists Add to cart (remove)
	5.	[Turner syndrome]. [electronic resource] by Monney, C Pescia, G Addor, M C Producer: 20001128 In: Schweizerische medizinische Wochenschrift vol. 130 Availability: No items available. Save to lists Add to cart (remove)
	6.	[Genetic aspects of fetal hydrops and cystic hygroma]. [electronic resource] by Fokstuen, S Pescia, G Addor, M C Producer: 19950209 In: Revue medicale de la Suisse romande vol. 114 Availability: No items available. Save to lists Add to cart (remove)
	7.	[The Vaud register of congenital abnormalities]. [electronic resource] by Addor, M C Pescia, G Marguerat, P Producer: 19930625 In: Revue medicale de la Suisse romande vol. 113 Availability: No items available. Save to lists Add to cart (remove)
	8.	Registration of congenital anomalies in Switzerland by EUROCAT. [electronic resource] by Addor, M C Pescia, G Schorderet, D F Producer: 20001128 In: Schweizerische medizinische Wochenschrift vol. 130 Availability: No items available. Save to lists Add to cart (remove)
	9.	[Hereditary multicentric osteolysis]. [electronic resource] by Addor, M C Pescia, G Egloff, D Quéloz, J Producer: 19861118 In: Journal de genetique humaine vol. 34 Availability: No items available. Save to lists Add to cart (remove)
	10.	[When genetic amniocentesis is misleading: apropos of a case of Jeune's syndrome]. [electronic resource] by Addor, M C Pescia, G Burgener, F Marguerat, P Producer: 19810922 In: Revue medicale de la Suisse romande vol. 101 Availability: No items available. Save to lists Add to cart (remove)
	11.	Screening for foetal malformations: performance of routine ultrasonography in the population of the Swiss Canton of Vaud. [electronic resource] by Vial, Y Tran, C Addor, M C Hohlfeld, P Producer: 20020220 In: Swiss medical weekly vol. 131 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	[Familial study of vesico-ureteral reflux]. [electronic resource] by Addor, M C Pescia, G Guignard, J P Genton, N Producer: 19840817 In: Journal de genetique humaine vol. 32 Availability: No items available. Save to lists Add to cart (remove)
	13.	An uncommon G375C substitution in a newborn with achondroplasia. [electronic resource] by Addor, M C Gudinchet, F Truttmann, A Schorderet, D F Producer: 20001121 In: Genetic counseling (Geneva, Switzerland) vol. 11 Availability: No items available. Save to lists Add to cart (remove)
	14.	Partial trisomy 20q in a newborn with dextrocardia. [electronic resource] by Addor, M C Castagne, C Micheli, J L Schorderet, D F Producer: 20030425 In: Genetic counseling (Geneva, Switzerland) vol. 13 Availability: No items available. Save to lists Add to cart (remove)
	15.	Two brothers with atypical syndactylies, cerebellar atrophy and severe mental retardation. [electronic resource] by Schorderet, D F Addor, M C Maeder, Ph Roulet, E Junier, L Producer: 20030425 In: Genetic counseling (Geneva, Switzerland) vol. 13 Availability: No items available. Save to lists Add to cart (remove)
	16.	A characteristic EEG pattern in 4p-syndrome: case report and review of the literature. [electronic resource] by Zankl, A Addor, M C Maeder-Ingvar, M M Schorderet, D F Producer: 20010419 In: European journal of pediatrics vol. 160 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	[Fluorescent in situ hybridization (FISH). Diagnostic aide in certain chromosomal anomalies]. [electronic resource] by Zankl, A Addor, M C Thonney, F Gaide, A C Schorderet, D F Producer: 20000912 In: Revue medicale de la Suisse romande vol. 120 Availability: No items available. Save to lists Add to cart (remove)
	18.	A new case of Pfeiffer syndrome with mutation in FGFR2. [electronic resource] by Addor, M C Gudinchet, F Laurini, R N Pescia, G Schorderet, D F Producer: 19980326 In: Genetic counseling (Geneva, Switzerland) vol. 8 Availability: No items available. Save to lists Add to cart (remove)
	19.	[Alpha-fetoprotein and chromosome aberrations: what else? Results of a prospective study concerning 15,533 pregnancies]. [electronic resource] by Marguerat, P Weihs, D Pescia, G Gaide, A C Addor, M C Nguyen The, H Producer: 19930625 In: Revue medicale de la Suisse romande vol. 113 Availability: No items available. Save to lists Add to cart (remove)
	20.	Fatal outcome in a female monozygotic twin with X-linked hypohydrotic ectodermal dysplasia (XLHED) due to a de novo t(X;9) translocation with probable disruption of the EDA gene. [electronic resource] by Zankl, A Addor, M C Cousin, P Gaide, A C Gudinchet, F Schorderet, D F Producer: 20011004 In: European journal of pediatrics vol. 160 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 34 results.