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Results of search for 'au:"Fryns, J.-P."', page 8 of 56
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Authors
Borghgraef, M
Cassiman, J J
De Smet, L
Devriendt, K
Fryns, J P
Fryns, J-P
Kleczkowska, A
Legius, E
Lukusa, T
Moerman, P
Petit, P
Schrander-Stumpel, C
Swillen, A
Van Den Berghe, H
Van den Berghe, H
Vandenberghe, K
Vermeesch, J R
Vogels, A
Witters, I
van den Berghe, H
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Topics
Abnormalities, Multiple
Adolescent
Adult
Child
Child, Preschool
Chromosome Aberrations
Chromosome Deletion
Female
Humans
Infant
Infant, Newborn
Intellectual Disability
Karyotyping
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Phenotype
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abnormalities
diagnosis
genetics
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141.
The neurobiology of autism.
[electronic resource]
by
Potgieter, S T
Fryns, J P
Producer:
19991227
In:
Genetic counseling (Geneva, Switzerland)
vol. 10
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142.
Kabuki syndrome: description of a 2-year old Roumanian boy and review of the literature.
[electronic resource]
by
Ioan, D M
Fryns, J P
Producer:
20070621
In:
Genetic counseling (Geneva, Switzerland)
vol. 18
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143.
Factors which contribute to cytogenetic frequency of expression in families of fragile X females.
[electronic resource]
by
Fisch, G S
Fryns, J P
Producer:
19920716
In:
American journal of medical genetics
vol. 43
Online resources:
Available from publisher's website
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144.
Lens dislocation and optic nerve hypoplasia in ring chromosome 21 mosaicism.
[electronic resource]
by
Meire, F M
Fryns, J P
Producer:
19950309
In:
Annales de genetique
vol. 37
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145.
Retinitis pigmentosa in a young man with Noonan syndrome: further evidence that Noonan syndrome (NS) and the cardio-facio-cutaneous syndrome (CFC) are variable manifestations of the same entity?
[electronic resource]
by
Lorenzetti, M E
Fryns, J P
Producer:
19970219
In:
American journal of medical genetics
vol. 65
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146.
Structural chromosome rearrangements in couples with recurrent fetal wastage.
[electronic resource]
by
Fryns, J P
Van Buggenhout, G
Producer:
19990415
In:
European journal of obstetrics, gynecology, and reproductive biology
vol. 81
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147.
Windblown foot: a particular presentation of Proteus syndrome?
[electronic resource]
by
De Smet, L
Fryns, J P
Producer:
20060404
In:
Genetic counseling (Geneva, Switzerland)
vol. 16
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148.
Symbrachydactyly in Turner's syndrome.
[electronic resource]
by
De Smet, L
Fryns, J P
Producer:
19960325
In:
Genetic counseling (Geneva, Switzerland)
vol. 6
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149.
Inverted nipples in Robinow syndrome.
[electronic resource]
by
Lorenzetti, M H
Fryns, J P
Producer:
19960731
In:
Genetic counseling (Geneva, Switzerland)
vol. 7
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150.
Oligodontia in partial trisomy 9q syndrome.
[electronic resource]
by
Bailleul-Forestier, I
Fryns, J P
Producer:
20070508
In:
Genetic counseling (Geneva, Switzerland)
vol. 17
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151.
Unilateral radio-ulnar synostosis and idic-Y chromosome.
[electronic resource]
by
De Smet, L
Fryns, J P
Producer:
20090330
In:
Genetic counseling (Geneva, Switzerland)
vol. 19
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152.
On the association of Poland anomaly and primary microcephaly.
[electronic resource]
by
Fryns, J P
de Smet, L
Producer:
19950427
In:
Clinical dysmorphology
vol. 3
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153.
Proteus syndrome and unilateral congenital windblown hand deformity.
[electronic resource]
by
De Smet, L
Fryns, J P
Producer:
19940527
In:
American journal of medical genetics
vol. 49
Online resources:
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154.
Aarskog syndrome: severe neurological deficit with spastic hemiplegia resulting from perinatal cerebrovascular accidents in two non-related males.
[electronic resource]
by
Fryns, J P
Descheemaeker, M J
Producer:
19951130
In:
Clinical genetics
vol. 48
Online resources:
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155.
Congenital hydrocephalus: nosology and guidelines for clinical approach and genetic counselling.
[electronic resource]
by
Schrander-Stumpel, C
Fryns, J P
Producer:
19980723
In:
European journal of pediatrics
vol. 157
Online resources:
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156.
Costello syndrome in two siblings and minor manifestations in their mother. Further evidence for autosomal dominant inheritance?
[electronic resource]
by
Ioan, D M
Fryns, J P
Producer:
20030212
In:
Genetic counseling (Geneva, Switzerland)
vol. 13
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157.
Symbrachydactyly involving both the hand and foot.
[electronic resource]
by
De Smet, L
Fryns, J P
Producer:
19991103
In:
Clinical genetics
vol. 56
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158.
Congenital scalp defects associated with postaxial polydactyly.
[electronic resource]
by
Fryns, J P
Van den Berghe, H
Producer:
19791024
In:
Human genetics
vol. 49
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159.
8q24.12 Interstitial deletion in trichorhinophalangeal syndrome type I.
[electronic resource]
by
Fryns, J P
Van den Berghe, H
Producer:
19861125
In:
Human genetics
vol. 74
Online resources:
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160.
An asymmetric type of chondrodysplasia in an adult male. Another example of postzygotic mutation for an autosomal dominant gene?
[electronic resource]
by
Fryns, J P
van den Berghe, H
Producer:
19870212
In:
Clinical genetics
vol. 30
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