Your search returned 280 results.

Results
	121.	[Prenatal diagnosis of hemophilia A during the first trimester of pregnancy]. [electronic resource] by Vidaud, M Daffos, F Lescs, M C Parquet-Gernez, A Rosa, J Goossens, M Producer: 19860513 In: Presse medicale (Paris, France : 1983) vol. 15 Availability: No items available. Save to lists Add to cart (remove)
	122.	Functional analysis of Sox10 mutations found in human Waardenburg-Hirschsprung patients. [electronic resource] by Kuhlbrodt, K Schmidt, C Sock, E Pingault, V Bondurand, N Goossens, M Wegner, M Producer: 19981015 In: The Journal of biological chemistry vol. 273 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	123.	Molecular cloning and complete primary sequence of human erythrocyte porphobilinogen deaminase. [electronic resource] by Raich, N Romeo, P H Dubart, A Beaupain, D Cohen-Solal, M Goossens, M Producer: 19861001 In: Nucleic acids research vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	124.	Spectrum of growth hormone receptor mutations and associated haplotypes in Laron syndrome. [electronic resource] by Amselem, S Duquesnoy, P Duriez, B Dastot, F Sobrier, M L Valleix, S Goossens, M Producer: 19930702 In: Human molecular genetics vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	125.	Psoralen-modified oligonucleotide primers improve detection of mutations by denaturing gradient gel electrophoresis and provide an alternative to GC-clamping. [electronic resource] by Costes, B Girodon, E Ghanem, N Chassignol, M Thuong, N T Dupret, D Goossens, M Producer: 19930702 In: Human molecular genetics vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	126.	Twenty-four novel hemophilia B mutations revealed by rapid scanning of the whole factor IX gene in a French population sample. [electronic resource] by Ghanem, N Costes, B Martin, J Vidaud, M Rothschild, C Foyer-Gazengel, C Goossens, M Producer: 19940913 In: European journal of human genetics : EJHG vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	127.	Nine novel growth hormone receptor gene mutations in patients with Laron syndrome. [electronic resource] by Sobrier, M L Dastot, F Duquesnoy, P Kandemir, N Yordam, N Goossens, M Amselem, S Producer: 19970311 In: The Journal of clinical endocrinology and metabolism vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	128.	Exclusion of linkage between the collagenase gene and generalized recessive dystrophic epidermolysis bullosa phenotype. [electronic resource] by Hovnanian, A Duquesnoy, P Amselem, S Blanchet-Bardon, C Lathrop, M Dubertret, L Goossens, M Producer: 19911213 In: The Journal of clinical investigation vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	129.	Frequent occurrence of the CFTR intron 8 (TG)n 5T allele in men with congenital bilateral absence of the vas deferens. [electronic resource] by Costes, B Girodon, E Ghanem, N Flori, E Jardin, A Soufir, J C Goossens, M Producer: 19960223 In: European journal of human genetics : EJHG vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	130.	Human beta-globin gene polymorphisms characterized in DNA extracted from ancient bones 12,000 years old. [electronic resource] by Béraud-Colomb, E Roubin, R Martin, J Maroc, N Gardeisen, A Trabuchet, G Goosséns, M Producer: 19960201 In: American journal of human genetics vol. 57 Availability: No items available. Save to lists Add to cart (remove)
	131.	Mild clinical phenotype associated with R1158X/S549R(T-->G) CFTR genotype. [electronic resource] by Frossard, P M Abdelaziz, S A Hertecant, J Girodon, E Goossens, M Dawson, K P Producer: 20010125 In: Clinical genetics vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	132.	Exhaustive screening of exon 10 CFTR gene mutations and polymorphisms by denaturing gradient gel electrophoresis: applications to genetic counselling in cystic fibrosis. [electronic resource] by Ghanem, N Fanen, P Martin, J Conteville, P Yahia-Cherif, Z Vidaud, M Goossens, M Producer: 19920413 In: Molecular and cellular probes vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	133.	Molecular cloning of a cDNA sequence complementary to porphobilinogen deaminase mRNA from rat. [electronic resource] by Grandchamp, B Romeo, P H Dubart, A Raich, N Rosa, J Nordmann, Y Goossens, M Producer: 19841003 In: Proceedings of the National Academy of Sciences of the United States of America vol. 81 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	134.	Primary hyperparathyroidism in two cats. [electronic resource] by den Hertog, E Goossens, M M van der Linde-Sipman, J S Kooistra, H S Producer: 19970821 In: The veterinary quarterly vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	135.	Atypical sinusitis in adults must lead to looking for cystic fibrosis and primary ciliary dyskinesia. [electronic resource] by Coste, A Girodon, E Louis, S Prulière-Escabasse, V Goossens, M Peynègre, R Escudier, E Producer: 20040618 In: The Laryngoscope vol. 114 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	136.	Laron dwarfism and mutations of the growth hormone-receptor gene. [electronic resource] by Amselem, S Duquesnoy, P Attree, O Novelli, G Bousnina, S Postel-Vinay, M C Goossens, M Producer: 19891023 In: The New England journal of medicine vol. 321 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	137.	Clinical evaluation of the CF(12)m cystic fibrosis DNA diagnostic kit. [electronic resource] by Houdayer, C Cazeneuve, C Cougoureux, E Magnier, C Tredano, M Aymard, P Goossens, M Feldmann, D Producer: 19980616 In: Clinical chemistry vol. 44 Availability: No items available. Save to lists Add to cart (remove)
	138.	[Prenatal diagnosis of hemoglobinopathies]. [electronic resource] by Dubart, A Goossens, M Beuzard, Y Monplaisir, N Testa, U Henrion, R Dumez, Y Rosa, J Producer: 19800712 In: Nouvelle revue francaise d'hematologie vol. Suppl Availability: No items available. Save to lists Add to cart (remove)
	139.	A 5' splice-region G----C mutation in exon 1 of the human beta-globin gene inhibits pre-mRNA splicing: a mechanism for beta+-thalassemia. [electronic resource] by Vidaud, M Gattoni, R Stevenin, J Vidaud, D Amselem, S Chibani, J Rosa, J Goossens, M Producer: 19890316 In: Proceedings of the National Academy of Sciences of the United States of America vol. 86 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	140.	[Prenatal diagnosis of human hemoglobinopathies]. [electronic resource] by Dubart, A Goossens, M Beuzard, Y Monplaisir, N Dumez, Y Dubuisson, J Henrion, R Rosa, J Producer: 19830311 In: Reproduction, nutrition, developpement vol. 20 Availability: No items available. Save to lists Add to cart (remove)

First
Previous
1
2
3
4
5
6
7
8
9
10
Next
Last

Refine your search

Availability

Authors

Topics

Languages

Your search returned 280 results.