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Results of search for 'au:"Seemanová, E"', page 4 of 7
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Authors
Bartsch, O
Benesová, D
Dolezal, A
Dreyer, M
Goetz, P
Hoza, J
Hyánek, J
Kapras, J
Kress, W
Lesný, I
Losan, F
Macek, M
Nevsímalová, S
Passarge, E
Rüdiger, H W
Salichová, J
Schmidt, A
Seemanova, E
Seemanová, E
Sperling, K
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Abnormalities, Multiple
Adolescent
Adult
Child
Child, Preschool
Chromosome Aberrations
Chromosome Disorders
Female
Humans
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Infant, Newborn
Intellectual Disability
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diagnosis
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g d
German
Your search returned 133 results.
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61.
[The Saldin-Noonan syndrome].
[electronic resource]
by
Seemanová, E
Endler, P
Benesová, D
Svobodová, J
Salichová, J
Producer:
19781227
In:
Casopis lekaru ceskych
vol. 117
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62.
[Increased risk of malignancies in heterozygotes in families of patients with Nijmegen breakage syndrome].
[electronic resource]
by
Seemanová, E
Jarolím, P
Seeman, P
Varon, R
Sperling, K
Producer:
20060411
In:
Casopis lekaru ceskych
vol. 145
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63.
[The fragile chromosome X syndrome].
[electronic resource]
by
Seemanová, E
Passarge, E
Schmidt, A
Hyánek, J
Salichová, J
Producer:
19830119
In:
Casopis lekaru ceskych
vol. 121
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64.
Genetic linkage study between the loci for Duchenne and Becker muscular dystrophy and nine X-chromosomal DNA markers.
[electronic resource]
by
Wilichowski, E
Krawczak, M
Seemanova, E
Hanefeld, F
Schmidtke, J
Producer:
19870305
In:
Human genetics
vol. 75
Online resources:
Available from publisher's website
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65.
[Differential diagnosis of progressive muscular dystrophies using an expert computer system].
[electronic resource]
by
Maríková, T
Seemanová, E
Marík, V
Zdráhal, Z
Zicha, D
Producer:
19850319
In:
Casopis lekaru ceskych
vol. 124
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66.
[Screening for fragile X syndrome in handicapped boys].
[electronic resource]
by
Steinbicker, V
Missbach, D
Goetz, P
Subrt, I
Seemanová, E
Producer:
19921123
In:
Kinderarztliche Praxis
vol. 60
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67.
Clinical and biochemical characterization of syndromes associated with defects of the insulin receptor.
[electronic resource]
by
Dreyer, M
Seemanová, E
Schmidt-Preuss, U
Rüdiger, H W
Producer:
19961206
In:
Acta Universitatis Carolinae. Medica
vol. 38
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68.
Fetal face syndrome with mental retardation.
[electronic resource]
by
Seemanová, E
Jirásek, J E
Sevcíková, M
Jodl, J
Kreisinger, J
Producer:
19741004
In:
Humangenetik
vol. 23
Online resources:
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69.
[Amniocentesis in the prenatal diagnosis of inborn chromosomal and metabolic defects (author's transl)].
[electronic resource]
by
Zwinger, A
Jirásek, J E
Seemanová, E
Macek, M
Dyková, H
Producer:
19750523
In:
Ceskoslovenska gynekologie
vol. 39
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70.
[Larsen's syndrome].
[electronic resource]
by
Kuklík, M
Seemanová, E
Jodl, J
Handzel, J
Klán, Z
Benesová, D
Producer:
19790925
In:
Ceskoslovenska pediatrie
vol. 34
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71.
The Zimmermann-Laband syndrome.
[electronic resource]
by
Pfeiffer, R A
Seemanova, E
Süss, J
Müssig, D
Tietze, H U
Producer:
19920326
In:
Klinische Padiatrie
vol. 204
Online resources:
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72.
Familial microcephaly with normal intelligence, immunodeficiency, and risk for lymphoreticular malignancies: a new autosomal recessive disorder.
[electronic resource]
by
Seemanová, E
Passarge, E
Beneskova, D
Houstĕk, J
Kasal, P
Sevcíková, M
Producer:
19850528
In:
American journal of medical genetics
vol. 20
Online resources:
Available from publisher's website
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73.
X-chromosomal recessive microcephaly with epilepsy, spastic tetraplegia and absent abdominal reflexes. New variety of "Paine syndrome"?
[electronic resource]
by
Seemanová, E
Lesný, I
Hyánek, J
Brachfeld, K
Rössler, M
Prosková, M
Producer:
19740528
In:
Humangenetik
vol. 20
Online resources:
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74.
[The TAR syndrome in 3 unrelated children].
[electronic resource]
by
Seemanová, E
Spicáková, V
Kulovaný, E
Salichová, J
Veprek, P
Zwinger, A
Producer:
19860214
In:
Ceskoslovenska pediatrie
vol. 40
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75.
[Cystinuria and lysinuria in Down's syndrome].
[electronic resource]
by
Hyánek, J
Goetz, P
Hoza, J
Kubík, M
Seemanová, E
Sedlácková, M
Producer:
19710106
In:
Casopis lekaru ceskych
vol. 109
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76.
[Prenatal diagnosis of glycogenosis II.--Pompe's disease].
[electronic resource]
by
Macek, M
Tomásová, H
Hug, G
Reinsteinová, H
Seemanová, E
Salichová, J
Producer:
19780127
In:
Ceskoslovenska pediatrie
vol. 32
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77.
[Gonosomal recessive heredity of microcephaly with epilepsy and spastic quadruparesis. New variant of the so called Paine's dyndrome?].
[electronic resource]
by
Seemanová, E
Lesný, I
Hyánek, J
Brachfeld, K
Rössler, M
Prosková, M
Producer:
19740306
In:
Ceskoslovenska pediatrie
vol. 28
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78.
[Child of a mother with hyperphenylalaninemia].
[electronic resource]
by
Hyánek, J
Hoza, J
Dolezal, A
Vinsová, N
Seemanová, E
Rejmanová, E
Producer:
19721221
In:
Ceskoslovenska pediatrie
vol. 27
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79.
Hypocretin deficiency in Prader-Willi syndrome.
[electronic resource]
by
Nevsimalova, S
Vankova, J
Stepanova, I
Seemanova, E
Mignot, E
Nishino, S
Producer:
20050310
In:
European journal of neurology
vol. 12
Online resources:
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80.
[The 47,XXX syndrome in a family with the fragile X chromosome syndrome].
[electronic resource]
by
Seemanová, E
Schmidt, A
Subrt, I
Passarge, E
Macek, M
Nedomová, V
Producer:
19851004
In:
Casopis lekaru ceskych
vol. 124
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