Skip to main content
مکتبة رقمیه للعلوم الطبيه
Your cart is empty.
Cart
Lists
Your lists
Log in to create your own lists
Log in to your account
Your cookies
Search history
Search the catalog by:
Library catalog
Title
Author
Subject
ISBN
ISSN
Series
Call number
Search the catalog by keyword
Advanced search
Authority search
Tag cloud
Library
Log in to your account
Home
Advanced search
Results of search for 'au:"Van Oost, B A"', page 5 of 7
Refine your search
Availability
Limit to records with available items
Authors
Barth, P G
Bolhuis, P A
Breen, M
Brunner, H G
Dreesen, J C
Everts, R E
Monnens, L A
Oostra, B A
Ropers, H H
Rothuizen, J
Ruitenbeek, W
Smeets, H J
Smits, A P
Van Oost, B A
Versteeg, S A
Wieringa, B
van Bennekom, C A
van Oost, B A
van den Berg, L
van den Ouweland, A M
Show more
Show less
Topics
Adult
Animals
Base Sequence
Chromosome Mapping
DNA
Dogs
Female
Genetic Linkage
Genetic Markers
Humans
Male
Molecular Sequence Data
Mutation
Pedigree
Point Mutation
Polymerase Chain Reaction
X Chromosome
analysis
genetics
metabolism
Show more
Show less
Languages
Dutch
English
German
Your search returned 128 results.
Sort
First
Previous
1
2
3
4
5
6
7
Next
Last
Sort by:
Relevance
Popularity (most to least)
Popularity (least to most)
Author (A-Z)
Author (Z-A)
Call number (0-9 to A-Z)
Call number (Z-A to 9-0)
Publication/Copyright date: Newest to oldest
Publication/Copyright date: Oldest to newest
Acquisition date: Newest to oldest
Acquisition date: Oldest to newest
Title (A-Z)
Title (Z-A)
Unhighlight
Highlight
Select all
Clear all
Select titles to:
Add to cart
Add to list
New list
Place hold
Results
81.
Confirmation of X-linked inheritance and provisional mapping of the keratosis follicularis spinulosa decalvans gene on Xp in a large Dutch family.
[electronic resource]
by
Oosterwijk, J C
Nelen, M
Van Zandvoort, P M
Van Osch, L D
Oranje, A P
Wittebol-Post, D
Van Oost, B A
Producer:
19920629
In:
Ophthalmic paediatrics and genetics
vol. 13
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
82.
Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber hereditary optic neuropathy and hereditary spastic dystonia.
[electronic resource]
by
De Vries, D D
Went, L N
Bruyn, G W
Scholte, H R
Hofstra, R M
Bolhuis, P A
van Oost, B A
Producer:
19960718
In:
American journal of human genetics
vol. 58
Availability:
No items available.
Save to lists
Add to cart
(remove)
83.
DXS539, a polymorphic DNA marker proximal of the fragile-X gene.
[electronic resource]
by
Dreesen, J C
van den Hurk, J A
Smits, A P
van den Ouweland, A M
Markslag, P W
van Oost, B A
Producer:
19930419
In:
Human genetics
vol. 91
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
84.
Refined genetic and comparative physical mapping of the canine copper toxicosis locus.
[electronic resource]
by
van de Sluis, B
Kole, S
van Wolferen, M
Holmes, N G
Pearson, P L
Rothuizen, J
van Oost, B A
Wijmenga, C
Producer:
20000728
In:
Mammalian genome : official journal of the International Mammalian Genome Society
vol. 11
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
85.
The canine sarcoglycan delta gene: BAC clone contig assembly, chromosome assignment and interrogation as a candidate gene for dilated cardiomyopathy in Dobermann dogs.
[electronic resource]
by
Stabej, P
Leegwater, P A J
Imholz, S
Versteeg, S A
Zijlstra, C
Stokhof, A A
Domanjko-Petriè, A
van Oost, B A
Producer:
20060123
In:
Cytogenetic and genome research
vol. 111
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
86.
Linkage analysis of keratosis follicularis spinulosa decalvans, and regional assignment to human chromosome Xp21.2-p22.2.
[electronic resource]
by
Oosterwijk, J C
Nelen, M
van Zandvoort, P M
van Osch, L D
Oranje, A P
Wittebol-Post, D
van Oost, B A
Producer:
19920420
In:
American journal of human genetics
vol. 50
Availability:
No items available.
Save to lists
Add to cart
(remove)
87.
Benign familial hematuria due to mutation of the type IV collagen alpha4 gene.
[electronic resource]
by
Lemmink, H H
Nillesen, W N
Mochizuki, T
Schröder, C H
Brunner, H G
van Oost, B A
Monnens, L A
Smeets, H J
Producer:
19961104
In:
The Journal of clinical investigation
vol. 98
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
88.
A 4-base pair deletion in the mitochondrial cytochrome b gene associated with parkinsonism/MELAS overlap syndrome.
[electronic resource]
by
De Coo, I F
Renier, W O
Ruitenbeek, W
Ter Laak, H J
Bakker, M
Schägger, H
Van Oost, B A
Smeets, H J
Producer:
19990127
In:
Annals of neurology
vol. 45
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
89.
Multipoint linkage analysis of DXS369 and DXS304 in fragile X families.
[electronic resource]
by
van Oost, B A
Smits, A
Dreesen, J C
Smeets, D
Perdon, L
van Bennekom, C A
Dahl, N
Bakker, E
Oostra, B A
Producer:
19910521
In:
American journal of medical genetics
vol. 38
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
90.
The gene for spondyloepiphyseal dysplasia (SEDL) maps to Xp22 between DXS16 and DXS92.
[electronic resource]
by
Heuertz, S
Nelen, M
Wilkie, A O
Le Merrer, M
Delrieu, O
Larget-Piet, L
Tranebjaerg, L
Bick, D
Hamel, B
Van Oost, B A
Producer:
19940204
In:
Genomics
vol. 18
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
91.
Two polymorphisms at the DXS539 locus.
[electronic resource]
by
van den Hurk, J A
Dreesen, J C
van den Berg, H
van Bennekom, C A
van den Ouweland, A M
van Oost, B A
Producer:
19910611
In:
Nucleic acids research
vol. 19
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
92.
A radiation hybrid map of the X-chromosome of the dog (Canis familiaris).
[electronic resource]
by
Everts, R E
van Wolferen, M E
Versteeg, S A
Zijlstra, C
Engelen, J J M
Bosma, A A
Rothuizen, J
van Oost, B A
Producer:
20030404
In:
Cytogenetic and genome research
vol. 98
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
93.
Myotonic dystrophy is closely linked to the gene for muscle-type creatine kinase (CKMM).
[electronic resource]
by
Brunner, H G
Korneluk, R G
Coerwinkel-Driessen, M
MacKenzie, A
Smeets, H
Lambermon, H M
van Oost, B A
Wieringa, B
Ropers, H H
Producer:
19890512
In:
Human genetics
vol. 81
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
94.
Prenatal exclusion of choroideremia.
[electronic resource]
by
van den Hurk, J A
van Zandvoort, P M
Brunsmann, F
Pawlowitzki, I H
Holzgreve, W
Szabo, P
Cremers, F P
van Oost, B A
Producer:
19930208
In:
American journal of medical genetics
vol. 44
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
95.
Prader-Willi syndrome and Angelman syndrome in cousins from a family with a translocation between chromosomes 6 and 15.
[electronic resource]
by
Smeets, D F
Hamel, B C
Nelen, M R
Smeets, H J
Bollen, J H
Smits, A P
Ropers, H H
van Oost, B A
Producer:
19920327
In:
The New England journal of medicine
vol. 326
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
96.
Myopathology and a mitochondrial DNA deletion in the Pearson marrow and pancreas syndrome.
[electronic resource]
by
de Vries, D D
Buzing, C J
Ruitenbeek, W
van der Wouw, M P
Sperl, W
Sengers, R C
Trijbels, J M
van Oost, B A
Producer:
19930212
In:
Neuromuscular disorders : NMD
vol. 2
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
97.
The gene for X-linked myotubular myopathy is located in an 8 Mb region at the border of Xq27.3 and Xq28.
[electronic resource]
by
Janssen, E A
Hensels, G W
van Oost, B A
Hamel, B C
Kemp, S
Baas, F
Weber, J W
Barth, P G
Bolhuis, P A
Producer:
19950411
In:
Neuromuscular disorders : NMD
vol. 4
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
98.
Clinical phenotype of nephrogenic diabetes insipidus in females heterozygous for a vasopressin type 2 receptor mutation.
[electronic resource]
by
van Lieburg, A F
Verdijk, M A
Schoute, F
Ligtenberg, M J
van Oost, B A
Waldhauser, F
Dobner, M
Monnens, L A
Knoers, N V
Producer:
19950817
In:
Human genetics
vol. 96
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
99.
Fine mapping of the human biglycan (BGN) gene within the Xq28 region employing a hybrid cell panel.
[electronic resource]
by
Traupe, H
van den Ouweland, A M
van Oost, B A
Vogel, W
Vetter, U
Warren, S T
Rocchi, M
Darlison, M G
Ropers, H H
Producer:
19920730
In:
Genomics
vol. 13
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
100.
Analysis of the inheritance of white spotting and the evaluation of KIT and EDNRB as spotting loci in Dutch boxer dogs.
[electronic resource]
by
van Hagen, M A E
van der Kolk, J
Barendse, M A M
Imholz, S
Leegwater, P A J
Knol, B W
van Oost, B A
Producer:
20041214
In:
The Journal of heredity
vol. 95
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
First
Previous
1
2
3
4
5
6
7
Next
Last