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Results of search for 'au:"Fryns, J.-P."', page 3 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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41.
Melorheostosis and somatic mosaicism.
[electronic resource]
by
Fryns, J P
Producer:
19960129
In:
American journal of medical genetics
vol. 58
Online resources:
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42.
Syndromic forms of hydrometrocolpos.
[electronic resource]
by
Fryns, J P
Producer:
19970522
In:
Prenatal diagnosis
vol. 17
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43.
Y-chromosome mosaicism with ring Y-chromosome/idic(Y)(p11.2) and "normal" ovarian development.
[electronic resource]
by
Fryns, J P
Producer:
20020221
In:
Annales de genetique
vol. 44
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44.
Partial trisomy 4p and Brachmann-de Lange syndrome.
[electronic resource]
by
Fryns, J P
Producer:
20010222
In:
American journal of medical genetics
vol. 95
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45.
Hypersplenism and portal hypertension with vena porta thrombosis in cartilage-hair hypoplasia (metaphyseal chondrodysplasia, McKusick type, MIM *250250)
[electronic resource]
by
Fryns, J P
Producer:
20010208
In:
Genetic counseling (Geneva, Switzerland)
vol. 11
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46.
Penile agenesis as an isolated malformation: a rare example of sexual ambiguity at birth.
[electronic resource]
by
Fryns, J P
Producer:
20010208
In:
Genetic counseling (Geneva, Switzerland)
vol. 11
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47.
Postaxial polydactyly as heterozygote manifestation in Ellis-Van Creveld syndrome?
[electronic resource]
by
Fryns, J P
Producer:
19910923
In:
American journal of medical genetics
vol. 39
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48.
[Unmanageable hair syndrome associated with epilepsy, deafness and phalangeal aplasia, or William's syndrome?].
[electronic resource]
by
Fryns, J P
Producer:
19881012
In:
Archives francaises de pediatrie
vol. 45
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49.
[Essential osteolysis with carpal and tarsal onset].
[electronic resource]
by
Fryns, J P
Producer:
19830826
In:
Journal de genetique humaine
vol. 30 Suppl 5
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50.
Maternal autosomal translocation t(5;18)(q12;q11) and Edward's syndrome in the fetus.
[electronic resource]
by
Fryns, J P
Producer:
19860311
In:
Clinical genetics
vol. 28
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51.
Prenatal diagnosis and long survival of Fryns syndrome.
[electronic resource]
by
Fryns, J P
Producer:
19950602
In:
Prenatal diagnosis
vol. 15
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52.
Osteopenia, abnormal dentition, hydrops fetalis and communicating hydrocephalus: unusual early clinical signs in Coffin-Lowry syndrome.
[electronic resource]
by
Fryns, J P
Producer:
19970314
In:
Clinical genetics
vol. 50
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53.
Neuroblastoma in patients with constitutional chromosomal changes.
[electronic resource]
by
Fryns, J P
Producer:
19960731
In:
Genetic counseling (Geneva, Switzerland)
vol. 7
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54.
Dolichomegasigmoid in Aarskog syndrome.
[electronic resource]
by
Fryns, J P
Producer:
19930203
In:
American journal of medical genetics
vol. 45
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55.
Syndrome of proximal interstitial deletion 4p15.
[electronic resource]
by
Fryns, J P
Producer:
19960130
In:
American journal of medical genetics
vol. 58
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56.
Gingival fibromatosis and partial duplication of the short arm of chromosome 2 (dup(2)(p13-->p21))
[electronic resource]
by
Fryns, J P
Producer:
19970917
In:
Annales de genetique
vol. 39
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57.
Progressive hydrocephalus in Noonan syndrome.
[electronic resource]
by
Fryns, J P
Producer:
19971209
In:
Clinical dysmorphology
vol. 6
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58.
Another holoprosencephaly locus at 7q21.2?
[electronic resource]
by
Fryns, J P
Producer:
19981001
In:
Journal of medical genetics
vol. 35
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59.
Genetic counseling and mental retardation: the role of special education in a multidisciplinary approach.
[electronic resource]
by
Borghgraef, M
Fryns, J P
Producer:
19931217
In:
Birth defects original article series
vol. 28
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60.
Schematic representation of NF-1 clinical features in French.
[electronic resource]
by
Legius, E
Fryns, J P
Producer:
19900614
In:
Neurofibromatosis
vol. 2
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