Results
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109.
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The gene for hereditary bullous dystrophy, X-linked macular type, maps to the Xq27.3-qter region. [electronic resource] by
- Wijker, M
- Ligtenberg, M J
- Schoute, F
- Defesche, J C
- Pals, G
- Bolhuis, P A
- Ropers, H H
- Hulsebos, T J
- Menko, F H
- van Oost, B A
Producer: 19950524
In:
American journal of human genetics vol. 56
Availability: No items available.
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110.
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111.
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112.
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Linkage homogeneity near the fragile X locus in normal and fragile X families. [electronic resource] by
- Suthers, G K
- Mulley, J C
- Voelckel, M A
- Dahl, N
- Väisänen, M L
- Steinbach, P
- Glass, I A
- Schwartz, C E
- van Oost, B A
- Thibodeau, S N
Producer: 19911017
In:
Genomics vol. 10
Availability: No items available.
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113.
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Characterization of a highly polymorphic dinucleotide repeat 150 KB proximal to the fragile X site. [electronic resource] by
- Riggins, G J
- Sherman, S L
- Oostra, B A
- Sutcliffe, J S
- Feitell, D
- Nelson, D L
- van Oost, B A
- Smits, A P
- Ramos, F J
- Pfendner, E
Producer: 19920716
In:
American journal of medical genetics vol. 43
Availability: No items available.
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114.
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Brief report: reverse mutation in myotonic dystrophy. [electronic resource] by
- Brunner, H G
- Jansen, G
- Nillesen, W
- Nelen, M R
- de Die, C E
- Höweler, C J
- van Oost, B A
- Wieringa, B
- Ropers, H H
- Smeets, H J
Producer: 19930218
In:
The New England journal of medicine vol. 328
Availability: No items available.
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115.
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Genetic mapping of new DNA probes at Xq27 defines a strategy for DNA studies in the fragile X syndrome. [electronic resource] by
- Suthers, G K
- Mulley, J C
- Voelckel, M A
- Dahl, N
- Väisänen, M L
- Steinbach, P
- Glass, I A
- Schwartz, C E
- van Oost, B A
- Thibodeau, S N
Producer: 19910403
In:
American journal of human genetics vol. 48
Availability: No items available.
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116.
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Influence of sex of the transmitting parent as well as of parental allele size on the CTG expansion in myotonic dystrophy (DM). [electronic resource] by
- Brunner, H G
- Brüggenwirth, H T
- Nillesen, W
- Jansen, G
- Hamel, B C
- Hoppe, R L
- de Die, C E
- Höweler, C J
- van Oost, B A
- Wieringa, B
Producer: 19931119
In:
American journal of human genetics vol. 53
Availability: No items available.
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117.
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Identification of four novel mutations in the COL4A5 gene of patients with Alport syndrome. [electronic resource] by
- Lemmink, H H
- Schröder, C H
- Brunner, H G
- Nelen, M R
- Zhou, J
- Tryggvason, K
- Haagsma-Schouten, W A
- Roodvoets, A P
- Rascher, W
- van Oost, B A
Producer: 19931028
In:
Genomics vol. 17
Availability: No items available.
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118.
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119.
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Identification of a two base pair deletion in five unrelated families with adrenoleukodystrophy: a possible hot spot for mutations. [electronic resource] by
- Kemp, S
- Ligtenberg, M J
- van Geel, B M
- Barth, P G
- Wolterman, R A
- Schoute, F
- Sarde, C O
- Mandel, J L
- van Oost, B A
- Bolhuis, P A
Producer: 19940901
In:
Biochemical and biophysical research communications vol. 202
Availability: No items available.
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120.
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Myotonic dystrophy. Predictive value of normal results on clinical examination. [electronic resource] by
- Brunner, H G
- Smeets, H J
- Nillesen, W
- van Oost, B A
- van den Biezenbos, J B
- Joosten, E M
- Pinckers, A J
- Hamel, B C
- Theeuwes, A G
- Wieringa, B
Producer: 19911226
In:
Brain : a journal of neurology vol. 114 ( Pt 5)
Availability: No items available.
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