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Results of search for 'au:"Oostra, R"', page 1 of 3
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Authors
Baljet, B
Beenen, L F M
Bilardo, C M
Bleeker-Wagemakers, E M
Bolhuis, P A
Dijkstra, P F
Duijst, W L J M
Hennekam, R C
Kerkhoffs, G M M J
Maas, M
Nikoskelainen, E
Norby, S
Oostra, R
Oostra, R J
Pajkrt, E
Poulton, J
Rosenberg, T
Van den Bogert, C
Wijburg, F A
van Rijn, R R
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Topics
Abnormalities, Multiple
Adolescent
Adult
Aged
Child
DNA Mutational Analysis
DNA, Mitochondrial
Female
History, 19th Century
Humans
Infant, Newborn
Male
Middle Aged
Museums
Netherlands
Optic Atrophies, Hereditary
Pedigree
Point Mutation
diagnosis
genetics
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Languages
Dutch
English
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1.
A primer for proficiency testing.
[electronic resource]
by
Oostra, R
Producer:
19860930
In:
MLO: medical laboratory observer
vol. 18
Availability:
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2.
Seldom-run tests: are you reliable or liable?
[electronic resource]
by
Oostra, R
Producer:
19870814
In:
MLO: medical laboratory observer
vol. 19
Availability:
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3.
On the road with a consulting technologist.
[electronic resource]
by
Oostra, R
Hofer, B
Producer:
19860703
In:
MLO: medical laboratory observer
vol. 18
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4.
Six steps to deal with complaints about lab service.
[electronic resource]
by
Oostra, R
Young, L
Producer:
19890109
In:
MLO: medical laboratory observer
vol. 20
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5.
Digital data and the 19th century teratology collection.
[electronic resource]
by
Baljet, B
Oostra, R J
Producer:
20000517
In:
The Journal of audiovisual media in medicine
vol. 22
Online resources:
Available from publisher's website
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6.
No violins, no apologies necessary: considering a career as a rural hospital executive.
[electronic resource]
by
Kiecker, C J
Oostra, R
Producer:
19910122
In:
Healthcare executive
vol. 5
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7.
Historical aspects of the study of malformations in The Netherlands.
[electronic resource]
by
Baljet, B
Oostra, R J
Producer:
19980624
In:
American journal of medical genetics
vol. 77
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8.
Brachmann-de Lange syndrome "avant la lettre".
[electronic resource]
by
Oostra, R J
Baljet, B
Hennekam, R C
Producer:
19950131
In:
American journal of medical genetics
vol. 52
Online resources:
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9.
Severe acrofacial dysostosis with orofacial clefting and tetraphocomelia diagnosed in the plaster cast of a 100-year-old anatomical specimen.
[electronic resource]
by
Oostra, R J
Baljet, B
Hennekam, R C
Producer:
19980924
In:
American journal of medical genetics
vol. 78
Online resources:
Available from publisher's website
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10.
Congenital anomalies in the teratological collection of Museum Vrolik in Amsterdam, The Netherlands. IV: closure defects of the neural tube.
[electronic resource]
by
Oostra, R J
Baljet, B
Hennekam, R C
Producer:
19990107
In:
American journal of medical genetics
vol. 80
Online resources:
Available from publisher's website
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11.
[Severe complications following an adeno-tonsillectomy in a patient with Hunter's syndrome (MPS II)].
[electronic resource]
by
Oostra, R J
Beentjes, B I
Bakker, H D
Producer:
19920507
In:
Tijdschrift voor kindergeneeskunde
vol. 60
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12.
Mitochondrial DNA analysis as a diagnostic tool in singleton cases of Leber's hereditary optic neuropathy.
[electronic resource]
by
Oostra, R J
Bolhuis, P A
Bleeker-Wagemakers, E M
Producer:
19940331
In:
Ophthalmic paediatrics and genetics
vol. 14
Online resources:
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13.
Congenital anomalies in the teratological collection of Museum Vrolik in Amsterdam, The Netherlands. II: Skeletal dysplasias.
[electronic resource]
by
Oostra, R J
Baljet, B
Dijkstra, P F
Hennekam, R C
Producer:
19980624
In:
American journal of medical genetics
vol. 77
Availability:
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14.
Absence of the spleen(s) in conjoined twins: a diagnostic clue of laterality defects? Radiological study of historical specimens.
[electronic resource]
by
Oostra, R J
Keulen, N
Jansen, T
van Rijn, R R
Producer:
20121031
In:
Pediatric radiology
vol. 42
Online resources:
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15.
Smith-Lemli-Opitz syndrome diagnosed in a 130-year-old anatomical specimen.
[electronic resource]
by
Oostra, R J
Baljet, B
Schutgens, R B
Hennekam, R C
Producer:
19970410
In:
American journal of medical genetics
vol. 68
Online resources:
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16.
Congenital anomalies in the teratological collection of Museum Vrolik in Amsterdam, The Netherlands. III: primary field defects, sequences, and other complex anomalies.
[electronic resource]
by
Oostra, R J
Baljet, B
Verbeeten, B W
Hennekam, R C
Producer:
19990107
In:
American journal of medical genetics
vol. 80
Online resources:
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17.
Congenital anomalies in the teratological collection of Museum Vrolik in Amsterdam, The Netherlands. I: Syndromes with multiple congenital anomalies.
[electronic resource]
by
Oostra, R J
Baljet, B
Dijkstra, P F
Hennekam, R C
Producer:
19980624
In:
American journal of medical genetics
vol. 77
Availability:
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18.
Congenital anomalies in the teratological collection of Museum Vrolik in Amsterdam, The Netherlands. V: conjoined and acardiac twins.
[electronic resource]
by
Oostra, R J
Baljet, B
Verbeeten, B W
Hennekam, R C
Producer:
19990107
In:
American journal of medical genetics
vol. 80
Availability:
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19.
No evidence for 'skewed' inactivation of the X-chromosome as cause of Leber's hereditary optic neuropathy in female carriers.
[electronic resource]
by
Oostra, R J
Kemp, S
Bolhuis, P A
Bleeker-Wagemakers, E M
Producer:
19961203
In:
Human genetics
vol. 97
Online resources:
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20.
Relationship between bullet diameter and bullet defect diameter in human calvariums.
[electronic resource]
by
Kerkhoff, W
Mattijssen, E J A T
Zwanenburg, E A
Oostra, R J
Producer:
20200914
In:
International journal of legal medicine
vol. 134
Online resources:
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