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Results of search for 'au:"Fryns, J.-P."', page 6 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
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Infant, Newborn
Intellectual Disability
Karyotyping
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abnormalities
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genetics
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101.
Thrombocytopenia in the Brachmann-de Lange syndrome.
[electronic resource]
by
Fryns, J P
Vinken, L
Producer:
19940708
In:
American journal of medical genetics
vol. 49
Online resources:
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102.
Pure de novo 17q25.3 micro duplication characterized by micro array CGH in a dysmorphic infant with growth retardation, developmental delay and distal arthrogryposis.
[electronic resource]
by
Lukusa, T
Fryns, J P
Producer:
20100514
In:
Genetic counseling (Geneva, Switzerland)
vol. 21
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103.
Unknown syndrome: abnormal facies, hypothyroidism, and severe retardation: a second patient.
[electronic resource]
by
Fryns, J P
Moerman, P
Producer:
19881117
In:
Journal of medical genetics
vol. 25
Online resources:
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104.
Population cytogenetics of autosomal fragile sites.
[electronic resource]
by
Fryns, J P
Petit, P
Producer:
19870608
In:
Clinical genetics
vol. 31
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105.
Apparently new autosomal recessive syndrome of mental retardation, distal limb deficiencies, oral involvement, and possible renal defect.
[electronic resource]
by
Buttiens, M
Fryns, J P
Producer:
19871001
In:
American journal of medical genetics
vol. 27
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106.
New lethal acrofacial dysostosis syndrome.
[electronic resource]
by
Fryns, J P
Kleckowska, A
Producer:
19910802
In:
American journal of medical genetics
vol. 39
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107.
Mucosal neuromata syndrome (MEN type IIb (III)).
[electronic resource]
by
Fryns, J P
Chrzanowska, K
Producer:
19890406
In:
Journal of medical genetics
vol. 25
Online resources:
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108.
Autism and ring chromosome 18 mosaicism.
[electronic resource]
by
Fryns, J P
Kleczkowska, A
Producer:
19921008
In:
Clinical genetics
vol. 42
Online resources:
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109.
Mental retardation, short stature, minor skeletal anomalies, craniofacial dysmorphism and macrodontia in two sisters and their mother. Another variant example of the KBG syndrome?
[electronic resource]
by
Fryns, J P
Haspeslagh, M
Producer:
19841003
In:
Clinical genetics
vol. 26
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110.
Two pericentric inversions inv(7)(p15;q32) and inv(9)(p11;q13) in a male with absence of vas deferens.
[electronic resource]
by
Petit, P
Fryns, J P
Producer:
19831028
In:
Human genetics
vol. 64
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111.
[Lethal skeletal dysplasias: delineation of a new distinct entity with spondylocostal dysostosis, multiple internal abnormalities and Dandy-Walker cyst].
[electronic resource]
by
Fryns, J P
Moerman, P
Producer:
19851219
In:
Journal de genetique humaine
vol. 33
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112.
Velo-facio-skeletal syndrome versus Aarskog syndrome.
[electronic resource]
by
Fryns, J P
Devriendt, K
Producer:
19970718
In:
American journal of medical genetics
vol. 64
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113.
Neurodevelopmental changes with age in Ullrich-Turner syndrome.
[electronic resource]
by
Swillen, A
Fryns, J P
Producer:
19960805
In:
American journal of medical genetics
vol. 61
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114.
Miller postaxial acrofacial dysostosis syndrome. Follow-up data of a family and confirmation of autosomal recessive inheritance.
[electronic resource]
by
Chrzanowska, K
Fryns, J P
Producer:
19931021
In:
Clinical genetics
vol. 43
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115.
Anophthalmia/microphtalmia associated with right lateral facial cleft/microtia.
[electronic resource]
by
Fryns, J P
Witters, I
Producer:
20020128
In:
Genetic counseling (Geneva, Switzerland)
vol. 12
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116.
The velocardiofacial syndrome: a review.
[electronic resource]
by
Vogels, A
Fryns, J P
Producer:
20030103
In:
Genetic counseling (Geneva, Switzerland)
vol. 13
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117.
Mental retardation, sparse hair, facial dysmorphism with a prominent lower lip, and lipodystrophy. A variant example of Nicolaides-Baraitser syndrome?
[electronic resource]
by
Witters, I
Fryns, J P
Producer:
20031104
In:
Genetic counseling (Geneva, Switzerland)
vol. 14
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118.
Popliteal pterygium and multiple pterygium syndromes.
[electronic resource]
by
Fryns, J P
Moerman, P
Producer:
20010726
In:
American journal of medical genetics
vol. 100
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119.
Syndrome of facial, oral, and digital anomalies due to 7q21.2-->q22.1 duplication.
[electronic resource]
by
Lukusa, T
Fryns, J P
Producer:
19990310
In:
American journal of medical genetics
vol. 80
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120.
X-linked mental retardation with marfanoid habitus.
[electronic resource]
by
Fryns, J P
Buttiens, M
Producer:
19880202
In:
American journal of medical genetics
vol. 28
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