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Results of search for 'au:"Smeets, E"', page 1 of 4
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Authors
Abraham-Inpijn, L
Bevers, E M
Bos, A A
Buurman, W A
Claessens, F
Comfurius, P
Curfs, L
Devlieger, H
Eggermont, E
Fryns, J P
Geutjens, J
Kleczkowska, A
Leeuwenberg, J F
Smeets, E
Smeets, E E J
Smeets, E F
Smeets, E H
Thiry, P
Van den Berghe, H
Zwaal, R F
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Abnormalities, Multiple
Adult
Animals
Female
Humans
Infant, Newborn
Intellectual Disability
Karyotyping
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Middle Aged
Netherlands
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abnormalities
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diagnosis
genetics
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1.
Benchmarking initiatives in the water industry.
[electronic resource]
by
Parena, R
Smeets, E
Producer:
20020117
In:
Water science and technology : a journal of the International Association on Water Pollution Research
vol. 44
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2.
"Cataplexy" in Coffin-Lowry syndrome.
[electronic resource]
by
Fryns, J P
Smeets, E
Producer:
19981113
In:
Journal of medical genetics
vol. 35
Online resources:
Available from publisher's website
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3.
Performance of a three-part dif impedance cytometer (Sysmex E-4000) in comparison with a cytochemical cytometer (Technicon H 6000).
[electronic resource]
by
Smeets, E H
van Wersch, J W
Producer:
19890323
In:
Journal of clinical chemistry and clinical biochemistry. Zeitschrift fur klinische Chemie und klinische Biochemie
vol. 26
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4.
Partial distal trisomy 3p. A partial autosomal trisomy without major dysmorphic features.
[electronic resource]
by
Smeets, E
Vandenbossche, L
Fryns, J P
Producer:
20010726
In:
Genetic counseling (Geneva, Switzerland)
vol. 12
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5.
Automation of the prothrombin time assay on a centrifugal analyser using two different chromogenic substrate reagents.
[electronic resource]
by
Smeets, E H
van Wersch, J W
Producer:
19890505
In:
Journal of clinical chemistry and clinical biochemistry. Zeitschrift fur klinische Chemie und klinische Biochemie
vol. 26
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6.
A NADH-dependent transketolase assay in erythrocyte hemolysates.
[electronic resource]
by
Smeets, E H
Muller, H
de Wael, J
Producer:
19720125
In:
Clinica chimica acta; international journal of clinical chemistry
vol. 33
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7.
Regional Proteus syndrome and somatic mosaicism.
[electronic resource]
by
Smeets, E
Fryns, J P
Cohen, M M
Producer:
19940808
In:
American journal of medical genetics
vol. 51
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8.
Rett Syndrome.
[electronic resource]
by
Smeets, E E J
Pelc, K
Dan, B
Publication details:
Molecular syndromology
Apr 2012
In:
Molecular syndromology
vol. 2
Online resources:
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9.
Melkersson-Rosenthal syndrome and de novo autosomal t(9;21)(p11;p11) translocation.
[electronic resource]
by
Smeets, E
Fryns, J P
Van den Berghe, H
Producer:
19941027
In:
Clinical genetics
vol. 45
Online resources:
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10.
Wolf-Hirschhorn syndrome with cryptic 4p16.3 deletion and balanced/unbalanced mosaicism in the mother.
[electronic resource]
by
Fryns, J P
Smeets, E
Devriendt, K
Petit, P
Producer:
19980917
In:
Annales de genetique
vol. 41
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11.
The Floating-Harbor syndrome: report of another patient and differential diagnosis with Shprintzen syndrome.
[electronic resource]
by
Smeets, E
Fryns, J P
Van den Berghe, H
Producer:
19961217
In:
Genetic counseling (Geneva, Switzerland)
vol. 7
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12.
On the nosology of the "primary true microcephaly, chorioretinal dysplasia, lymphoedema" association.
[electronic resource]
by
Fryns, J P
Smeets, E
Van den Berghe, H
Producer:
19960228
In:
Clinical genetics
vol. 48
Online resources:
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13.
The 24-hour pattern of urinary MHPG excretion in depressives and normals.
[electronic resource]
by
Van Bemmel, A L
Smeets, E H
Van Diest, R
Producer:
19890112
In:
Acta psychiatrica Scandinavica
vol. 78
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14.
New progress in placentography and renography by scanning with technetium-99m labelled compounds.
[electronic resource]
by
Woldring, M G
Smeets, E H
van Zanten, A K
Producer:
19681005
In:
Nuclear-Medizin
vol. 6
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15.
Detecting the medically compromised patient in dentistry by means of the medical risk-related history. A survey of 29,424 dental patients in The Netherlands.
[electronic resource]
by
Smeets, E C
de Jong, K J
Abraham-Inpijn, L
Producer:
19981014
In:
Preventive medicine
vol. 27
Online resources:
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16.
Acute medical complications in 277 general dental practices.
[electronic resource]
by
Smeets, E C
Keur, I
Oosting, J
Abraham-Inpijn, L
Producer:
19990603
In:
Preventive medicine
vol. 28
Online resources:
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17.
Small terminal 10q26 deletion in a male patient with Noonan-like stigmata: diagnosis by cytogenetic and FISH analysis.
[electronic resource]
by
Lukusa, T
Smeets, E
Vermeesch, J R
Fryns, J P
Producer:
20030425
In:
Genetic counseling (Geneva, Switzerland)
vol. 13
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18.
Contribution of different phospholipid classes to the prothrombin converting capacity of sonicated lipid vesicles.
[electronic resource]
by
Smeets, E F
Comfurius, P
Bevers, E M
Zwaal, R F
Producer:
19970306
In:
Thrombosis research
vol. 81
Online resources:
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19.
Noonan phenotype in the basal cell nevus syndrome.
[electronic resource]
by
Grubben, C
Fryns, J P
Smeets, E
Van den Berghe, H
Producer:
19920113
In:
Genetic counseling (Geneva, Switzerland)
vol. 2
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20.
Distal 11q deletion: a specific clinical entity.
[electronic resource]
by
Fryns, J P
Kleczkowska, A
Smeets, E
Van den Berghe, H
Producer:
19880212
In:
Helvetica paediatrica acta
vol. 42
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