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Results of search for 'au:"Fryns, J.-P."', page 12 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
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Chromosome Aberrations
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221.
Skin pigmentation anomalies in ring chromosome 13.
[electronic resource]
by
Fryns, J P
Devriendt, K
Legius, E
Producer:
19980922
In:
Genetic counseling (Geneva, Switzerland)
vol. 9
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222.
Follow-up of an adult with Keutel syndrome.
[electronic resource]
by
Devriendt, K
Holvoet, M
Fryns, J P
Producer:
19990720
In:
American journal of medical genetics
vol. 85
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223.
Conductive hearing loss and multiple pre- and supra-auricular skin defects: a variant example of the Branchio-Oculo-Facial syndrome.
[electronic resource]
by
Vantrappen, G
Feenstra, L
Fryns, J P
Producer:
20010208
In:
Genetic counseling (Geneva, Switzerland)
vol. 11
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224.
Polysyndactyly and trigonocephaly with partial agenesis of corpus callosum: an example of the variable clinical spectrum of the Acrocallosal syndrome?
[electronic resource]
by
Fryns, J P
Devriendt, K
Legius, E
Producer:
19970922
In:
Clinical dysmorphology
vol. 6
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225.
Increased nuchal translucency thickness in thrombocytopenia-absent-radius syndrome.
[electronic resource]
by
Witters, I
Claerhout, P
Fryns, J P
Producer:
20060203
In:
Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology
vol. 26
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226.
Skeletal dysplasias: 38 prenatal cases.
[electronic resource]
by
Witters, I
Moerman, Ph
Fryns, J P
Producer:
20090123
In:
Genetic counseling (Geneva, Switzerland)
vol. 19
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227.
Von Recklinghausen-neurofibromatosis: a study of the psychological profile.
[electronic resource]
by
Spaepen, A
Borghgraef, M
Fryns, J P
Producer:
19931217
In:
Birth defects original article series
vol. 28
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228.
On the occurrence of macroorchidism and mental handicap in the Aarskog syndrome.
[electronic resource]
by
Fryns, J P
Van den Berghe, H
Producer:
19900410
In:
Journal de genetique humaine
vol. 37
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229.
Fragile X expression and X inactivation. I. The expression of the fragile site at Xq27.3 is not suppressed on inactive X chromosomes separated from the active homologue.
[electronic resource]
by
Wöhrle, D
Fryns, J P
Steinbach, P
Producer:
19901226
In:
Human genetics
vol. 85
Online resources:
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230.
Is the expression of fra(2)(q13) age dependent?
[electronic resource]
by
Fryns, J P
Van den Berghe, H
Producer:
19890406
In:
Journal of medical genetics
vol. 25
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231.
Mid-trimester ultrasonographic diagnosis of early manifesting "adult" form of polycystic kidney disease.
[electronic resource]
by
Fryns, J P
Vandenberghe, K
Moerman, F
Producer:
19870211
In:
Human genetics
vol. 74
Online resources:
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232.
Ring chromosome 22 in a mentally retarded child and mosaic 45,XX,-15,-22,+t(15;22)(p11;q11)/46,XX,r(22)/46,XX karyotype in the mother.
[electronic resource]
by
Fryns, J P
Van den Berghe, H
Producer:
19790725
In:
Human genetics
vol. 47
Online resources:
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233.
Trisomy 18 syndrome.
[electronic resource]
by
Fryns, J P
Van den Berghe, H
Producer:
19781220
In:
Acta paediatrica Belgica
vol. 31
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234.
Trisomy 12p due to familial t(12p-,6q plus) translocation.
[electronic resource]
by
Fryns, J P
Van Den Berghe, H
Producer:
19750421
In:
Humangenetik
vol. 24
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235.
Progressive extrapyramidal disorder with primary hypogonadism and alopecia in sibs: a new syndrome?
[electronic resource]
by
Devriendt, K
Legius, E
Fryns, J P
Producer:
19960919
In:
American journal of medical genetics
vol. 62
Online resources:
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236.
Maternal serum positive triple test screening in a fetus with partial distal trisomy 7p associated with maternal 7p;18p translocation.
[electronic resource]
by
Witters, I
Moerman, P
Fryns, J P
Producer:
20021129
In:
Genetic counseling (Geneva, Switzerland)
vol. 13
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237.
Unusual chromosomal mosaicism in Wolf-Hirschhorn syndrome: del(4)(p16)/der(4)(qter-q31.3::pter-qter).
[electronic resource]
by
Syrrou, M
Borghgraef, M
Fryns, J P
Producer:
20020115
In:
American journal of medical genetics
vol. 104
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238.
The prenatal diagnosis of spinal muscular atrophy.
[electronic resource]
by
Matthijs, G
Devriendt, K
Fryns, J P
Producer:
19980929
In:
Prenatal diagnosis
vol. 18
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239.
Prenatal echographic diagnosis of laryngeal atresia as part of a multiple congenital anomalies (MCA) syndrome.
[electronic resource]
by
Witters, I
Moerman, P
Fryns, J P
Producer:
20010208
In:
Genetic counseling (Geneva, Switzerland)
vol. 11
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240.
The XYY syndrome: a follow-up study on 38 boys.
[electronic resource]
by
Geerts, M
Steyaert, J
Fryns, J P
Producer:
20040224
In:
Genetic counseling (Geneva, Switzerland)
vol. 14
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