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Results of search for 'au:"Fryns, J.-P."', page 20 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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381.
On the nosology of the "primary true microcephaly, chorioretinal dysplasia, lymphoedema" association.
[electronic resource]
by
Fryns, J P
Smeets, E
Van den Berghe, H
Producer:
19960228
In:
Clinical genetics
vol. 48
Online resources:
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382.
Prenatal diagnosis of trisomy 21 between 1991 and 1999 in the Leuven Centre for Human Genetics: effect of triple test screening.
[electronic resource]
by
Witters, I
Legius, E
Matthijs, G
Fryns, J P
Producer:
20030103
In:
Genetic counseling (Geneva, Switzerland)
vol. 13
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383.
Severe primary pulmonary hypoplasia ("acinar dysplasia") in sibs: a genetically determined mesodermal defect?
[electronic resource]
by
Moerman, P
Vanhole, C
Devlieger, H
Fryns, J P
Producer:
19990204
In:
Journal of medical genetics
vol. 35
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384.
Sporadic case of bilateral fusion of metacarpal 4 and 5.
[electronic resource]
by
Debeer, P H
De Smedt, M
Fryns, J-P
Producer:
20040928
In:
American journal of medical genetics. Part A
vol. 125A
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385.
The cardio-facio-cutaneous (CFC) syndrome: autosomal dominant inheritance in a large family.
[electronic resource]
by
Fryns, J P
Volcke, P
Van den Berghe, H
Producer:
19920701
In:
Genetic counseling (Geneva, Switzerland)
vol. 3
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386.
Cohen syndrome: fertility in a female patient.
[electronic resource]
by
Fryns, J P
Lemmens, F
van den Berghe, H
Producer:
19920312
In:
Clinical genetics
vol. 40
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387.
Congenital scalp defect with distal limb reduction anomalies.
[electronic resource]
by
Fryns, J P
Corbeel, L
Van den Berghe, H
Producer:
19780218
In:
European journal of pediatrics
vol. 126
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388.
Martin-Bell phenotype in males with acquired central nervous system lesions. 15 males diagnosed during a systematic etiological study of 274 mentally retarded males.
[electronic resource]
by
Fryns, J P
Volcke, P
Van Den Berghe, H
Producer:
19910503
In:
Genetic counseling (Geneva, Switzerland)
vol. 1
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389.
Cardio-facio-cutaneous (CFC) syndrome: report of a new patient.
[electronic resource]
by
Chrzanowska, K
Fryns, J P
Van den Berghe, H
Producer:
19900123
In:
American journal of medical genetics
vol. 33
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390.
47,XXY karyotype in a patient with Beckwith-Wiedemann syndrome.
[electronic resource]
by
Fryns, J P
Kleczkowska, A
Van den Berghe, H
Producer:
19861107
In:
Annales de genetique
vol. 29
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391.
Autosomal whole arm translocations in man. A patient with t(5p7p;5q7q) type rearrangement and review of the literature.
[electronic resource]
by
Kleczkowska, A
Fryns, J P
van den Berghe, H
Producer:
19861118
In:
Clinical genetics
vol. 30
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392.
Psychological findings in three children with ring 15 chromosome.
[electronic resource]
by
Borghgraef, M
Fryns, J P
Van den Berghe, H
Producer:
19890228
In:
Journal of mental deficiency research
vol. 32 ( Pt 4)
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393.
8-trisomy syndrome.
[electronic resource]
by
Fryns, J P
Boussuyt, C
van den Berghe, H
Producer:
19770630
In:
Acta paediatrica Belgica
vol. 30
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394.
Osteodysplasty a rare skeletal dysplasia.
[electronic resource]
by
Fryns, J P
Maertens, R
Van Den Berghe, H
Producer:
19790816
In:
Acta paediatrica Belgica
vol. 32
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395.
Gonadoblastoma and Y-chromosome fluorescence.
[electronic resource]
by
Lukusa, T
Fryns, J P
van den Berghe, H
Producer:
19860725
In:
Clinical genetics
vol. 29
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396.
Diaphragmatic defects, craniofacial dysmorphism, cleft palate and distal limb deformities. - a new lethal syndrome.
[electronic resource]
by
Goddeeris, P
Fryns, J P
van den Berghe, H
Producer:
19801024
In:
Journal de genetique humaine
vol. 28
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397.
Internal male pseudohermaphroditism in a 6 week old child.
[electronic resource]
by
Lukusa, T
Fryns, J P
Van den Berghe, H
Producer:
19870330
In:
European journal of pediatrics
vol. 145
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398.
Macrocephaly, distinct craniofacial appearance and spastic paraplegia: an autosomal recessive subtype of complicated spastic paraplegia.
[electronic resource]
by
Fryns, J P
Hellemans, M
Van den Berghe, H
Producer:
19941004
In:
Clinical genetics
vol. 45
Online resources:
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399.
Personality profile in adult female fragile X carriers: assessed with the Minnesota Multiphasic Personality Profile (MMPI).
[electronic resource]
by
Steyaert, J
Decruyenaere, M
Borghgraef, M
Fryns, J P
Producer:
19941116
In:
American journal of medical genetics
vol. 51
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400.
Autism and genetics: high incidence of specific genetic syndromes in 21 autistic adolescents and adults living in two residential homes in Belgium.
[electronic resource]
by
Swillen, A
Hellemans, H
Steyaert, J
Fryns, J P
Producer:
19961203
In:
American journal of medical genetics
vol. 67
Online resources:
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