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Results of search for 'au:"Fryns, J.-P."', page 1 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
Male
Phenotype
Pregnancy
Syndrome
abnormalities
diagnosis
genetics
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English
French
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1.
[Balanced chromosome abnormalities with abnormal phenotype].
[electronic resource]
by
Fryns, J P
Producer:
19880725
In:
Journal de genetique humaine
vol. 36
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2.
The female and the fragile X. A study of 144 obligate female carriers.
[electronic resource]
by
Fryns, J P
Producer:
19860404
In:
American journal of medical genetics
vol. 23
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3.
Autosomal dominant simple microphthalmos: incomplete penetrance and variable expression in a large family.
[electronic resource]
by
Fryns, J P
Producer:
19950918
In:
Journal of medical genetics
vol. 32
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4.
Major central nervous system malformation in "micromelic dwarfism with cone epiphyses, metaphyseal dysplasia and vertebral segmentation defects".
[electronic resource]
by
Fryns, J P
Producer:
19970318
In:
American journal of medical genetics
vol. 68
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5.
Trichorhinophalangeal syndrome type 2: another syndromic form of hydrometrocolpos.
[electronic resource]
by
Fryns, J P
Producer:
19980212
In:
American journal of medical genetics
vol. 73
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6.
Trisomy 9p and tetrasomy 9p: a unique, clinically recognisable syndrome.
[electronic resource]
by
Fryns, J P
Producer:
19981202
In:
Genetic counseling (Geneva, Switzerland)
vol. 9
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7.
Mental status and psychosocial functioning in XYY males.
[electronic resource]
by
Fryns, J P
Producer:
19980610
In:
Prenatal diagnosis
vol. 18
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8.
Meier-Gorlin syndrome: the adult phenotype.
[electronic resource]
by
Fryns, J P
Producer:
19981015
In:
Clinical dysmorphology
vol. 7
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9.
X-linked mental retardation with marfanoid habitus.
[electronic resource]
by
Fryns, J P
Producer:
19910521
In:
American journal of medical genetics
vol. 38
Online resources:
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10.
Fountain's syndrome: mental retardation, sensorineural deafness, skeletal abnormalities, and coarse face with full lips.
[electronic resource]
by
Fryns, J P
Producer:
19891226
In:
Journal of medical genetics
vol. 26
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11.
The Prader-Willi syndrome and the Sotos syndrome: syndromes or sequences?
[electronic resource]
by
Fryns, J P
Producer:
19881122
In:
Clinical genetics
vol. 33
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12.
Fryns syndrome: a variable MCA syndrome with diaphragmatic defects, coarse face, and distal limb hypoplasia.
[electronic resource]
by
Fryns, J P
Producer:
19870720
In:
Journal of medical genetics
vol. 24
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13.
The concurrence of the blepharophimosis, ptosis, epicanthus inversus syndrome (BPES) and Langer type of mesomelic dwarfism in the same patient. Evidence of the location of Langer type of mesomelic dwarfism at 3q22.3-q23?
[electronic resource]
by
Fryns, J P
Producer:
19951214
In:
Clinical genetics
vol. 48
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14.
Previously apparently undescribed syndrome: shallow orbits, ptosis, coloboma, trigonocephaly, gyral malformations, and mental and growth retardation.
[electronic resource]
by
Fryns, J P
Producer:
19961227
In:
American journal of medical genetics
vol. 64
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15.
Acalvaria and occipital scalp defects.
[electronic resource]
by
Fryns, J P
Producer:
19940708
In:
American journal of medical genetics
vol. 49
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16.
Serpentine fibula syndrome: a variant clinical presentation of Hajdu-Cheney syndrome?
[electronic resource]
by
Fryns, J P
Producer:
19970922
In:
Clinical dysmorphology
vol. 6
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17.
MCA/MR syndrome with severe pre- and postnatal growth retardation, deep mental retardation, distinct facial appearance with nasal hypoplasia, cleft palate and retino-choroidal coloboma in two unrelated female patients.
[electronic resource]
by
Fryns, J P
Producer:
20010215
In:
Genetic counseling (Geneva, Switzerland)
vol. 11
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18.
Follow-up of 16q deletions.
[electronic resource]
by
Fryns, J P
Producer:
19910125
In:
American journal of medical genetics
vol. 37
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19.
[Posterolateral diaphragmatic hernia and Brachmann-de-Lange syndrome].
[electronic resource]
by
Fryns, J P
Producer:
19870901
In:
Archives francaises de pediatrie
vol. 44
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20.
Congenital scalp defects with distal limb reduction anomalies.
[electronic resource]
by
Fryns, J P
Producer:
19871110
In:
Journal of medical genetics
vol. 24
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