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Results of search for 'au:"Legius, E"', page 3 of 8
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Authors
Andersen, L B
Brems, H
Casaer, P
Cassiman, J J
Collins, F S
Cuppens, H
Descheemaeker, M J
Devriendt, K
Eggermont, E
Evers-Kiebooms, G
Fryns, J P
Glover, T W
Legius, E
Marynen, P
Matthijs, G
Moerman, P
Proesmans, W
Schollen, E
Van den Berghe, H
Vogels, A
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Abnormalities, Multiple
Adolescent
Adult
Base Sequence
Child
Child, Preschool
Female
Humans
Infant
Intellectual Disability
Male
Middle Aged
Molecular Sequence Data
Neurofibromatosis 1
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abnormalities
complications
diagnosis
genetics
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41.
Oculo-auriculo-vertebral spectrum malformation and contralateral absence of internal carotid artery.
[electronic resource]
by
Legius, E
Hellemans, M
Wilms, G
Tillemans, B
Fryns, J P
Producer:
19940330
In:
Genetic counseling (Geneva, Switzerland)
vol. 4
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42.
Marden-Walker phenotype: a diagnostic dilemma.
[electronic resource]
by
Soekarman, D
Volcke, P
Legius, E
Holvoet, M
Fryns, J P
Producer:
19960731
In:
Genetic counseling (Geneva, Switzerland)
vol. 7
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43.
Genetic abnormalities and male infertility. A comprehensive review.
[electronic resource]
by
Thielemans, B F
Spiessens, C
D'Hooghe, T
Vanderschueren, D
Legius, E
Producer:
19990415
In:
European journal of obstetrics, gynecology, and reproductive biology
vol. 81
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44.
The cardiofaciocutaneous syndrome: prenatal findings in two patients.
[electronic resource]
by
Witters, I
Denayer, E
Brems, H
Fryns, J P
Legius, E
Producer:
20080519
In:
Prenatal diagnosis
vol. 28
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45.
BRCA1/2 predictive testing and gender: uptake, motivation and psychological characteristics.
[electronic resource]
by
Denayer, L
Boogaerts, A
Philippe, K
Legius, E
Evers-Kiebooms, G
Producer:
20100318
In:
Genetic counseling (Geneva, Switzerland)
vol. 20
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46.
EEC syndrome without ectrodactyly: report of two new families.
[electronic resource]
by
Fryns, J P
Legius, E
Dereymaeker, A M
Van den Berghe, H
Producer:
19900515
In:
Journal of medical genetics
vol. 27
Online resources:
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47.
Neurofibromatosis type 1.
[electronic resource]
by
Legius, E
Descheemaeker, M J
Fryns, J P
Van den Berghe, H
Producer:
19950209
In:
Genetic counseling (Geneva, Switzerland)
vol. 5
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48.
NF2 gene deletion in a family with a mild phenotype.
[electronic resource]
by
López-Correa, C
Zucman-Rossi, J
Brems, H
Thomas, G
Legius, E
Producer:
20000218
In:
Journal of medical genetics
vol. 37
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49.
Two adult females with a distinct familial mental retardation syndrome: non-progressive neurological symptoms with ataxia and hypotonia, similar facial appearance, hypergonadotrophic hypogonadism, and retinal dystrophy.
[electronic resource]
by
Fryns, J P
Van Lingen, C
Devriendt, K
Legius, E
Raus, P
Producer:
19980630
In:
Journal of medical genetics
vol. 35
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50.
Increased frequency of chromosomal abnormalities in female partners of couples undergoing in vitro fertilization or intracytoplasmic sperm injection.
[electronic resource]
by
Schreurs, A
Legius, E
Meuleman, C
Fryns, J P
D'Hooghe, T M
Producer:
20000802
In:
Fertility and sterility
vol. 74
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51.
Neurofibromatosis type 1 in childhood: a study of the neuropsychological profile in 45 children.
[electronic resource]
by
Legius, E
Descheemaeker, M J
Spaepen, A
Casaer, P
Fryns, J P
Producer:
19940812
In:
Genetic counseling (Geneva, Switzerland)
vol. 5
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52.
Prophylactic salpingo-oophorectomy in 51 women with familial breast-ovarian cancer: importance of fallopian tube dysplasia.
[electronic resource]
by
Leunen, K
Legius, E
Moerman, P
Amant, F
Neven, P
Vergote, I
Producer:
20060517
In:
International journal of gynecological cancer : official journal of the International Gynecological Cancer Society
vol. 16
Online resources:
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53.
Medullary thyroid carcinoma in a child with a new RET mutation and a RET polymorphism.
[electronic resource]
by
Vandenbosch, K
Renard, M
Uyttebroeck, A
Sciot, R
Matthijs, G
Legius, E
Producer:
20050802
In:
Genetic counseling (Geneva, Switzerland)
vol. 16
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54.
Behavioural, academic and neuropsychological profile of normally gifted Neurofibromatosis type 1 children.
[electronic resource]
by
Descheemaeker, M-J
Ghesquière, P
Symons, H
Fryns, J P
Legius, E
Producer:
20050510
In:
Journal of intellectual disability research : JIDR
vol. 49
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55.
Prenatal indomethacin toxicity in one member of monozygous twins; a case report.
[electronic resource]
by
Demandt, E
Legius, E
Devlieger, H
Lemmens, F
Proesmans, W
Eggermont, E
Producer:
19900613
In:
European journal of obstetrics, gynecology, and reproductive biology
vol. 35
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56.
Alpha-1-proteinase inhibitor gene frequencies in Belgium.
[electronic resource]
by
Kimpen, J
Legius, E
Bosmans, E
Van Vaerenbergh, V
Ramon, A
Raus, J
Producer:
19911113
In:
Gene geography : a computerized bulletin on human gene frequencies
vol. 4
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57.
Syndrome of myxomas, spotty skin pigmentation, and endocrine overactivity (Carney complex).
[electronic resource]
by
Legius, E
Daenen, W
Vandenbergh, V
Verbeeck, G
Bex, M
Fryns, J P
Producer:
19990414
In:
Genetic counseling (Geneva, Switzerland)
vol. 9
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58.
Muscular hypertrophy of the oesophagus and "Alport-like" glomerular lesions in a boy.
[electronic resource]
by
Legius, E
Proesmans, W
Van Damme, B
Geboes, K
Lerut, T
Eggermont, E
Producer:
19900828
In:
European journal of pediatrics
vol. 149
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59.
Rickets due to dietary calcium deficiency.
[electronic resource]
by
Legius, E
Proesmans, W
Eggermont, E
Vandamme-Lobaerts, R
Bouillon, R
Smet, M
Producer:
19891102
In:
European journal of pediatrics
vol. 148
Online resources:
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60.
Patients with High-Grade Gliomas and Café-au-Lait Macules: Is Neurofibromatosis Type 1 the Only Diagnosis?
[electronic resource]
by
Guerrini-Rousseau, L
Suerink, M
Grill, J
Legius, E
Wimmer, K
Brugières, L
Producer:
20200113
In:
AJNR. American journal of neuroradiology
vol. 40
Online resources:
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