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Results of search for 'au:"Hoefnagels, M"'
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Authors
D'Hondt, F
Dereymaeker, A
Dereymaeker, A M
Dereymaker, A M
Fryns, J P
Heremans, G
Hoefnagels, M
Hoefnagels, M A
Hoefnagels, M H
Kleczkowska, A
Linderman, R G
Marien, J
Mertens, G
Van den Berghe, H
Volcke, P
de Vries, R A
van Leusen, R
van den Berghe, H
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Topics
Abnormalities, Multiple
Adolescent
Adult
Central Nervous System Diseases
Child
Child, Preschool
Chromosome Aberrations
Face
Female
Fragile X Syndrome
Genes, Dominant
Humans
Intellectual Disability
Male
Pedigree
Syndrome
abnormalities
complications
diagnosis
genetics
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Your search returned 9 results.
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1.
Biological Suppression of Seedborne Fusarium spp. During Cold Stratification of Douglas Fir Seeds.
[electronic resource]
by
Hoefnagels, M H
Linderman, R G
Publication details:
Plant disease
Sep 1999
In:
Plant disease
vol. 83
Online resources:
Available from publisher's website
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No items available.
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2.
[Three patients with weight loss as a result of sarcoidosis presenting as liver disease].
[electronic resource]
by
Hoefnagels, M A
van Leusen, R
de Vries, R A
Producer:
20040224
In:
Nederlands tijdschrift voor geneeskunde
vol. 147
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No items available.
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3.
Mental retardation, deafness, skeletal abnormalities, and coarse face with full lips: confirmation of the Fountain syndrome.
[electronic resource]
by
Fryns, J P
Dereymaeker, A
Hoefnagels, M
Van den Berghe, H
Producer:
19870514
In:
American journal of medical genetics
vol. 26
Online resources:
Available from publisher's website
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4.
Partial fra(X) phenotype with megalotestes in fra (X)-negative patients with acquired lesions of the central nervous system.
[electronic resource]
by
Fryns, J P
Dereymaeker, A
Hoefnagels, M
Volcke, P
Van den Berghe, H
Producer:
19860404
In:
American journal of medical genetics
vol. 23
Online resources:
Available from publisher's website
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5.
The Brachmann-de Lange syndrome in two siblings of normal parents.
[electronic resource]
by
Fryns, J P
Dereymaeker, A M
Hoefnagels, M
D'Hondt, F
Mertens, G
van den Berghe, H
Producer:
19870930
In:
Clinical genetics
vol. 31
Online resources:
Available from publisher's website
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6.
The Opitz hypertelorism-hypospadias syndrome. Further delineation of the spectrum of clinical findings.
[electronic resource]
by
Dereymaeker, A M
Fryns, J P
Hoefnagels, M
Heremans, G
Marien, J
Van den Berghe, H
Producer:
19871120
In:
Journal de genetique humaine
vol. 35
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7.
The Borjeson-Forssman-Lehmann syndrome. A family study.
[electronic resource]
by
Dereymaeker, A M
Fryns, J P
Hoefnagels, M
Heremans, G
Marien, J
van den Berghe, H
Producer:
19860725
In:
Clinical genetics
vol. 29
Availability:
No items available.
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8.
A genetic-diagnostic survey in an institutionalized population of 173 severely mentally retarded patients.
[electronic resource]
by
Fryns, J P
Kleczkowska, A
Dereymaeker, A
Hoefnagels, M
Heremans, G
Marien, J
van den Berghe, H
Producer:
19870212
In:
Clinical genetics
vol. 30
Online resources:
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9.
Partial 8p trisomy due to interstitial duplication: karyotype: 46, XX, inv dup(8) (p21.1----p22).
[electronic resource]
by
Fryns, J P
Kleczkowska, A
Dereymaker, A M
Hoefnagels, M
Heremans, G
Marien, J
van den Berghe, H
Producer:
19860219
In:
Clinical genetics
vol. 28
Online resources:
Available from publisher's website
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