Results
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21.
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Alternative splicing in the fragile X gene FMR1. [electronic resource] by
- Verkerk, A J
- de Graaff, E
- De Boulle, K
- Eichler, E E
- Konecki, D S
- Reyniers, E
- Manca, A
- Poustka, A
- Willems, P J
- Nelson, D L
Producer: 19931105
In:
Human molecular genetics vol. 2
Availability: No items available.
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22.
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A point mutation in the FMR-1 gene associated with fragile X mental retardation. [electronic resource] by
- De Boulle, K
- Verkerk, A J
- Reyniers, E
- Vits, L
- Hendrickx, J
- Van Roy, B
- Van den Bos, F
- de Graaff, E
- Oostra, B A
- Willems, P J
Producer: 19930611
In:
Nature genetics vol. 3
Availability: No items available.
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23.
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Refinement of the multiple exostoses locus (EXT2) to a 3-cM interval on chromosome 11. [electronic resource] by
- Wuyts, W
- Ramlakhan, S
- Van Hul, W
- Hecht, J T
- van den Ouweland, A M
- Raskind, W H
- Hofstede, F C
- Reyniers, E
- Wells, D E
- de Vries, B
Producer: 19951012
In:
American journal of human genetics vol. 57
Availability: No items available.
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24.
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Transgenic mouse model for the fragile X syndrome. [electronic resource] by
- Kooy, R F
- D'Hooge, R
- Reyniers, E
- Bakker, C E
- Nagels, G
- De Boulle, K
- Storm, K
- Clincke, G
- De Deyn, P P
- Oostra, B A
- Willems, P J
Producer: 19961213
In:
American journal of medical genetics vol. 64
Availability: No items available.
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25.
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Assignment of a second locus for multiple exostoses to the pericentromeric region of chromosome 11. [electronic resource] by
- Wu, Y Q
- Heutink, P
- de Vries, B B
- Sandkuijl, L A
- van den Ouweland, A M
- Niermeijer, M F
- Galjaard, H
- Reyniers, E
- Willems, P J
- Halley, D J
Producer: 19940523
In:
Human molecular genetics vol. 3
Availability: No items available.
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26.
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Multiplex ligation-dependent probe amplification to detect subtelomeric rearrangements in routine diagnostics. [electronic resource] by
- Rooms, L
- Reyniers, E
- Wuyts, W
- Storm, K
- van Luijk, R
- Scheers, S
- Wauters, J
- van den Ende, J
- Biervliet, M
- Eyskens, F
- van Goethem, G
- Laridon, A
- Ceulemans, B
- Courtens, W
- Kooy, R F
Producer: 20060612
In:
Clinical genetics vol. 69
Availability: No items available.
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27.
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Familial mental retardation syndrome ATR-16 due to an inherited cryptic subtelomeric translocation, t(3;16)(q29;p13.3). [electronic resource] by
- Holinski-Feder, E
- Reyniers, E
- Uhrig, S
- Golla, A
- Wauters, J
- Kroisel, P
- Bossuyt, P
- Rost, I
- Jedele, K
- Zierler, H
- Schwab, S
- Wildenauer, D
- Speicher, M R
- Willems, P J
- Meitinger, T
- Kooy, R F
Producer: 20000309
In:
American journal of human genetics vol. 66
Availability: No items available.
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28.
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L1 knockout mice show dilated ventricles, vermis hypoplasia and impaired exploration patterns. [electronic resource] by
- Fransen, E
- D'Hooge, R
- Van Camp, G
- Verhoye, M
- Sijbers, J
- Reyniers, E
- Soriano, P
- Kamiguchi, H
- Willemsen, R
- Koekkoek, S K
- De Zeeuw, C I
- De Deyn, P P
- Van der Linden, A
- Lemmon, V
- Kooy, R F
- Willems, P J
Producer: 19980619
In:
Human molecular genetics vol. 7
Availability: No items available.
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29.
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Positional cloning of a gene involved in hereditary multiple exostoses. [electronic resource] by
- Wuyts, W
- Van Hul, W
- Wauters, J
- Nemtsova, M
- Reyniers, E
- Van Hul, E V
- De Boulle, K
- de Vries, B B
- Hendrickx, J
- Herrygers, I
- Bossuyt, P
- Balemans, W
- Fransen, E
- Vits, L
- Coucke, P
- Nowak, N J
- Shows, T B
- Mallet, L
- van den Ouweland, A M
- McGaughran, J
- Halley, D J
- Willems, P J
Producer: 19970204
In:
Human molecular genetics vol. 5
Availability: No items available.
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30.
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Distal myopathy with upper limb predominance caused by filamin C haploinsufficiency. [electronic resource] by
- Guergueltcheva, V
- Peeters, K
- Baets, J
- Ceuterick-de Groote, C
- Martin, J J
- Suls, A
- De Vriendt, E
- Mihaylova, V
- Chamova, T
- Almeida-Souza, L
- Ydens, E
- Tzekov, C
- Hadjidekov, G
- Gospodinova, M
- Storm, K
- Reyniers, E
- Bichev, S
- van der Ven, P F M
- Fürst, D O
- Mitev, V
- Lochmüller, H
- Timmerman, V
- Tournev, I
- De Jonghe, P
- Jordanova, A
Producer: 20120209
In:
Neurology vol. 77
Availability: No items available.
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