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Results of search for 'au:"Smeets, D F"', page 1 of 3
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Authors
Assman-Hulsmans, C F
Beck, J L
Brunner, H G
Govaerts, L C
Hamel, B C
Haraldsson, A
Hopman, A H
Hustinx, T W
Jap, P H
Kremer, H
Merkx, G F
Mieloo, H
Poels, L G
Ramaekers, F C
Ropers, H H
Scheres, J M
Smeets, D F
Smeets, D F C M
Smits, A P
Weemaes, C M
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Topics
Abnormalities, Multiple
Adolescent
Adult
Child
Child, Preschool
Chromosome Aberrations
Chromosome Fragility
Female
Humans
Infant
Intellectual Disability
Karyotyping
Male
Middle Aged
Pedigree
Phenotype
Syndrome
Translocation, Genetic
abnormalities
genetics
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English
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1.
Low level of mosaicism for a balanced translocation as a case of unbalanced offspring.
[electronic resource]
by
Smeets, D F
Producer:
19930203
In:
American journal of medical genetics
vol. 45
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2.
Neither age nor sex influence the expression of folate sensitive common fragile sites on human chromosomes.
[electronic resource]
by
Smeets, D F
Merkx, G
Producer:
19910123
In:
Human genetics
vol. 86
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3.
Common fragile sites in man and three closely related primate species.
[electronic resource]
by
Smeets, D F
van de Klundert, F A
Producer:
19900521
In:
Cytogenetics and cell genetics
vol. 53
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4.
Frequent occurrence of translocations of the short arm of chromosome 15 to other D-group chromosomes.
[electronic resource]
by
Smeets, D F
Merkx, G F
Hopman, A H
Producer:
19910702
In:
Human genetics
vol. 87
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5.
The fragile site on chromosome 3.
[electronic resource]
by
Smeets, D F
Scheres, J M
Hustinx, T W
Producer:
19841025
In:
Human genetics
vol. 67
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6.
Heritable fragility at 11q13 and 12q13.
[electronic resource]
by
Smeets, D F
Scheres, J M
Hustinx, T W
Producer:
19851119
In:
Clinical genetics
vol. 28
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7.
The most common fragile site in man is 3p14.
[electronic resource]
by
Smeets, D F
Scheres, J M
Hustinx, T W
Producer:
19860505
In:
Human genetics
vol. 72
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8.
Chromosome 15p marker D15Z1 frequently maps to the short arm of other D-group chromosomes.
[electronic resource]
by
Smeets, D F
Merkx, G F
Hopman, A H
Producer:
19920304
In:
Human genetics
vol. 88
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9.
Nijmegen Breakage syndrome: a progress report.
[electronic resource]
by
Weemaes, C M
Smeets, D F
van der Burgt, C J
Producer:
19950224
In:
International journal of radiation biology
vol. 66
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10.
Immunological studies in Bloom's syndrome. A follow-up report.
[electronic resource]
by
Weemaes, C M
Bakkeren, J A
Haraldsson, A
Smeets, D F
Producer:
19920521
In:
Annales de genetique
vol. 34
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11.
Evidence for specificity of the DA/DAPI technique.
[electronic resource]
by
Merkx, G F
Hopman, A H
Akkermans-Scholten, A C
Smeets, D F
Producer:
19910116
In:
Cytogenetics and cell genetics
vol. 54
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12.
Variants of Nijmegen breakage syndrome and ataxia telangiectasia.
[electronic resource]
by
Weemaes, C M
Smeets, D F
Horstink, M
Haraldsson, A
Bakkeren, J A
Producer:
19940527
In:
Immunodeficiency
vol. 4
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13.
Submicroscopic interstitial deletion of the X chromosome explains a complex genetic syndrome dominated by Norrie disease.
[electronic resource]
by
Gal, A
Wieringa, B
Smeets, D F
Bleeker-Wagemakers, L
Ropers, H H
Producer:
19861104
In:
Cytogenetics and cell genetics
vol. 42
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14.
A phenotypical male infant with 46,X,der(Y)t(X;Y)(?;p11) de novo.
[electronic resource]
by
Govaerts, L C
Draaisma, J M
vd Blij-Philipsen, M
Smeets, D F
Producer:
19970610
In:
Annales de genetique
vol. 40
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15.
Penetrance estimate of the fra(X) gene using Pointer versus direct estimate.
[electronic resource]
by
de Haan, A F
Smits, A P
Smeets, D F
van Oost, B A
Producer:
19920716
In:
American journal of medical genetics
vol. 43
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16.
Unique mosaicism of structural chromosomal rearrangement: is chromosome 18 preferentially involved?
[electronic resource]
by
de Pater, J M
Smeets, D F C M
Scheres, J M J C
Producer:
20031224
In:
American journal of medical genetics. Part A
vol. 119A
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17.
Down-Turner syndrome: case report and review.
[electronic resource]
by
Van Buggenhout, G J
Hamel, B C
Trommelen, J C
Mieloo, H
Smeets, D F
Producer:
19950224
In:
Journal of medical genetics
vol. 31
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18.
Absent thumb, immune disorder, and congenital anemia presenting with hydrops fetalis.
[electronic resource]
by
Semmekrot, B A
Haraldsson, A
Weemaes, C M
Smeets, D F
Geven, W B
Brunner, H G
Producer:
19920818
In:
American journal of medical genetics
vol. 42
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19.
Late-onset ataxia telangiectasia in two brothers presenting with juvenile resting tremor.
[electronic resource]
by
Hiel, J A
Weemaes, C M
Smeets, D F
Van de Vlasakker, C J
Horstink, M W
Producer:
19941214
In:
Movement disorders : official journal of the Movement Disorder Society
vol. 9
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20.
Absence of karyotype abnormalities in patients with familial urothelial cell carcinoma.
[electronic resource]
by
Aben, K K
Macville, M V
Smeets, D F
Schoenberg, M P
Witjes, J A
Kiemeney, L A
Producer:
20010405
In:
Urology
vol. 57
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