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Results of search for 'au:"D'Espallier, L"'
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Authors
Baert, A L
D'Espallier, L
Devriendt, K
Fryns, J P
Gilis, F
Marchal, G
Moerman, P
Ponette, E
Trimpeneers, F
Van den Berghe, H
Vandepitte, J
Wuyts, F
d'Espallier, L
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Topics
Adolescent
Adult
Anemia, Hypochromic
Brain
Central Nervous System
Child, Preschool
Chronic Disease
Ectoderm
Facial Bones
Female
Fragile X Syndrome
Genes, Dominant
Hemangioma
Heterozygote
Humans
Male
Pregnancy
complications
etiology
genetics
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English
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1.
Mental retardation, distinct craniofacial dysmorphism, and central nervous system malformation: confirmation of a syndrome.
[electronic resource]
by
Devriendt, K
D'Espallier, L
Fryns, J P
Producer:
19961010
In:
Journal of medical genetics
vol. 33
Online resources:
Available from publisher's website
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No items available.
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2.
Suggestively increased rate of infant death in children of fra(X) positive mothers.
[electronic resource]
by
Fryns, J P
Moerman, P
Gilis, F
d'Espallier, L
Van den Berghe, H
Producer:
19881108
In:
American journal of medical genetics
vol. 30
Online resources:
Available from publisher's website
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No items available.
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3.
Intestinal hemangioma causing anemia in a child.
[electronic resource]
by
Wuyts, F
Ponette, E
Marchal, G
Baert, A L
D'Espallier, L
Trimpeneers, F
Vandepitte, J
Producer:
19821218
In:
Journal belge de radiologie
vol. 65
Availability:
No items available.
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