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Results of search for 'au:"Fryns, J.-P."', page 4 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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Abnormalities, Multiple
Adolescent
Adult
Child
Child, Preschool
Chromosome Aberrations
Chromosome Deletion
Female
Humans
Infant
Infant, Newborn
Intellectual Disability
Karyotyping
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abnormalities
diagnosis
genetics
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61.
Ring chromosome 21 in a normal female.
[electronic resource]
by
Kleczkowska, A
Fryns, J P
Producer:
19840910
In:
Annales de genetique
vol. 27
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62.
Expression of fragile site at 10q25 in normal culture conditions.
[electronic resource]
by
Petit, P
Fryns, J P
Producer:
19830324
In:
American journal of human genetics
vol. 35
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63.
Hypohidrotic ectodermal dysplasia, central nervous system malformation, and distinct facial features: confirmation of a distinct entity?
[electronic resource]
by
Soekarman, D
Fryns, J P
Producer:
19930520
In:
Journal of medical genetics
vol. 30
Online resources:
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64.
46,XY/46,XX mosaicism and congenital pulmonary lymphangiectasis with chylothorax.
[electronic resource]
by
Fryns, J P
Moerman, P
Producer:
19940204
In:
American journal of medical genetics
vol. 47
Online resources:
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65.
Hematometra and sudden death after status epilepticus in the adolescent female with Fryns syndrome.
[electronic resource]
by
Dingens, M
Fryns, J P
Producer:
20000106
In:
Genetic counseling (Geneva, Switzerland)
vol. 10
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66.
Prenatal diagnosis of central nervous system abnormalities: diagnostic possibilities and limitations of fetal neurosonography.
[electronic resource]
by
Witters, I
Fryns, J P
Producer:
20000512
In:
Genetic counseling (Geneva, Switzerland)
vol. 11
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67.
Hypoplastic claviculae in the Kabuki (Niikawa-Kuroki) syndrome.
[electronic resource]
by
Fryns, J P
Devriendt, K
Producer:
19980710
In:
Genetic counseling (Geneva, Switzerland)
vol. 9
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68.
The Prader-Willi syndrome and the Angelman syndrome.
[electronic resource]
by
Vogels, A
Fryns, J P
Producer:
20030425
In:
Genetic counseling (Geneva, Switzerland)
vol. 13
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69.
Age at diagnosis, body mass index and physical morbidity in children and adults with the Prader-Willi syndrome.
[electronic resource]
by
Vogels, A
Fryns, J P
Producer:
20050421
In:
Genetic counseling (Geneva, Switzerland)
vol. 15
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70.
Mosaic normal/unbalanced karyotype and recurrent fetal wastage.
[electronic resource]
by
Kleczkowska, A
Fryns, J P
Producer:
19900808
In:
American journal of medical genetics
vol. 36
Online resources:
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71.
The fetal akinesia deformation sequence. A fetopathological approach.
[electronic resource]
by
Moerman, P
Fryns, J P
Producer:
19901220
In:
Genetic counseling (Geneva, Switzerland)
vol. 1
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72.
Wolf-Hirschhorn and Cri du Chat syndromes resulting from familial translocations: 3 further examples of the Bp monosomy epistatic effect.
[electronic resource]
by
Petit, P
Fryns, J P
Producer:
19910503
In:
Genetic counseling (Geneva, Switzerland)
vol. 1
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73.
Holoprosencephaly and postaxial polydactyly: another observation.
[electronic resource]
by
Moerman, P
Fryns, J P
Producer:
19881117
In:
Journal of medical genetics
vol. 25
Online resources:
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74.
Abdominal distension in Kaufman-McKusick syndrome.
[electronic resource]
by
Fryns, J P
Moerman, P
Producer:
19871001
In:
American journal of medical genetics
vol. 27
Online resources:
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75.
Severe progressive neurological disorder associated with hydrocephalus in a man with fragile X syndrome.
[electronic resource]
by
Schaap, C
Fryns, J P
Producer:
19941116
In:
American journal of medical genetics
vol. 51
Online resources:
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76.
The Kabuki make-up (Niikawa-Kuroki) syndrome and isolated transient hyperphosphatasemia.
[electronic resource]
by
Devriendt, K
Fryns, J P
Producer:
19941027
In:
Clinical genetics
vol. 45
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77.
Corpus callosum agenesis in Coffin-Lowry syndrome.
[electronic resource]
by
Soekarman, D
Fryns, J P
Producer:
19940812
In:
Genetic counseling (Geneva, Switzerland)
vol. 5
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78.
Genetic locus on chromosome 6p for multicystic renal dysplasia, pelvi-ureteral junction stenosis, and vesicoureteral reflux.
[electronic resource]
by
Devriendt, K
Fryns, J P
Producer:
19960419
In:
American journal of medical genetics
vol. 59
Online resources:
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79.
Pure distal monosomy 10q26 in a patient displaying clinical features of Prader-Willi syndrome during infancy and distinct behavioural phenotype in adolescence.
[electronic resource]
by
Lukusa, T
Fryns, J P
Producer:
20001121
In:
Genetic counseling (Geneva, Switzerland)
vol. 11
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80.
On the nosology of van der Woude syndrome and popliteal pterygium syndrome: implications for genetic counseling.
[electronic resource]
by
Fryns, J P
Devriendt, K
Producer:
20000512
In:
Genetic counseling (Geneva, Switzerland)
vol. 11
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