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	41.	[Familial incidence of pericentric inversion of X chromosome]. [electronic resource] by Niebuhr, E Seemanová, E Losan, F Producer: 19750523 In: Ceskoslovenska pediatrie vol. 29 Availability: No items available. Save to lists Add to cart (remove)
	42.	[Manifestations of genetic burden in prenatal and postnatal periods]. [electronic resource] by Seemanová, E Macek, M Goetz, P Producer: 19720919 In: Ceskoslovenska pediatrie vol. 27 Availability: No items available. Save to lists Add to cart (remove)
	43.	Incidence of phenylketonuria and other inborn errors of the amino acid metabolism in the normal and mentally retarded population. [electronic resource] by Hyánek, J Homolka, J Seemanová, E Producer: 19740503 In: Review of Czechoslovak medicine vol. 20 Availability: No items available. Save to lists Add to cart (remove)
	44.	Autosomal dominant insulin resistance syndrome due to postbinding defect. [electronic resource] by Seemanová, E Rüdiger, H W Dreyer, M Producer: 19930208 In: American journal of medical genetics vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	45.	Morfan: a new syndrome characterized by mental retardation, pre- and postnatal overgrowth, remarkable face and acanthosis nigricans in 5-year-old boy. [electronic resource] by Seemanová, E Rüdiger, H W Dreyer, M Producer: 19930506 In: American journal of medical genetics vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	46.	[Childhood obesity as a symptom of genetic syndromes]. [electronic resource] by Seemanová, E Rüdiger, H W Dreyer, M Producer: 19890830 In: Ceskoslovenska pediatrie vol. 44 Availability: No items available. Save to lists Add to cart (remove)
	47.	[The Ellis-van Creveld syndrome in a boy (author's transl)]. [electronic resource] by Seemanová, E Kopecký, A Salichová, J Handzel, J Producer: 19790927 In: Casopis lekaru ceskych vol. 118 Availability: No items available. Save to lists Add to cart (remove)
	48.	[Hereditary incidence of cerebellar atrophy]. [electronic resource] by Krejcová, H Filipová, M Seemanová, E Jirásek, A Producer: 19760108 In: Ceskoslovenska neurologie a neurochirurgie vol. 38 Availability: No items available. Save to lists Add to cart (remove)
	49.	[Use of expert systems in the clinical genetics of polydactyly and progressive muscular dystrophies]. [electronic resource] by Maríková, T Seemanová, E Hrycejová, I Krautwurmová, H Producer: 19880311 In: Ceskoslovenska pediatrie vol. 42 Availability: No items available. Save to lists Add to cart (remove)
	50.	[Autosomal recessive pseudohypertonic muscular dystrophy with mental retardation. Report on 2 siblings]. [electronic resource] by Lesný, I Seemanová, E Kocura, P Prosková, M Producer: 19850103 In: Ceskoslovenska neurologie a neurochirurgie vol. 47 Availability: No items available. Save to lists Add to cart (remove)
	51.	[Familial incidence of Down's disease]. [electronic resource] by Goetz, P Svagrová, E Seemanová, E Macek, M Producer: 19730405 In: Ceskoslovenska pediatrie vol. 28 Availability: No items available. Save to lists Add to cart (remove)
	52.	[Fatal syndrome of multiple malformations in 3 siblings]. [electronic resource] by Povýsilová, V Macek, M Salichová, J Seemanová, E Producer: 19760823 In: Ceskoslovenska pediatrie vol. 31 Availability: No items available. Save to lists Add to cart (remove)
	53.	Duffy locus linkage and HLA antigens in hereditary motor-sensory neuropathy. [electronic resource] by Nevsímalová, S Prazák, J Herzog, P Seemanová, E Producer: 19910610 In: Schweizer Archiv fur Neurologie und Psychiatrie (Zurich, Switzerland : 1985) vol. 142 Availability: No items available. Save to lists Add to cart (remove)
	54.	[The "osteoporosis-pseudoglioma" syndrome]. [electronic resource] by Lomícková, H Seemanová, E Snobl, O Zoban, P Producer: 19841128 In: Ceskoslovenska oftalmologie vol. 40 Availability: No items available. Save to lists Add to cart (remove)
	55.	[Duffy blood groups and HLA antigens in hereditary motor-sensory neuropathy]. [electronic resource] by Nevsímalová, S Prazák, J Herzog, P Seemanová, E Producer: 19900613 In: Ceskoslovenska neurologie a neurochirurgie vol. 52 Availability: No items available. Save to lists Add to cart (remove)
	56.	Prenatal detection of a fetus hemizygous for the fragile X-chromosome. [electronic resource] by Schmidt, A Passarge, E Seemanová, E Macek, M Producer: 19830623 In: Human genetics vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	57.	The novel contiguous gene syndrome of myotubular myopathy (MTM1), male hypogenitalism and deletion in Xq28:report of the first familial case. [electronic resource] by Bartsch, O Kress, W Wagner, A Seemanova, E Producer: 19991015 In: Cytogenetics and cell genetics vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	58.	[Meckel's syndrome]. [electronic resource] by Seemanová, E Sevcíková, M Koubek, K Bresták, M Producer: 19760430 In: Ceskoslovenska pediatrie vol. 30 Availability: No items available. Save to lists Add to cart (remove)
	59.	[Our experience with genetic counseling]. [electronic resource] by Seemanová, E Saluchová, J Mocek, M Goetz, P Producer: 19740306 In: Ceskoslovenska pediatrie vol. 28 Availability: No items available. Save to lists Add to cart (remove)
	60.	X del(q) Turner's syndrome in a 30-month-old girl. [electronic resource] by Losan, F Macek, M Seemanová, E Zwinger, A Producer: 19771125 In: Human heredity vol. 27 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 133 results.