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Results of search for 'au:"Barr, D G"', page 2 of 2
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Authors
Ahmed, S F
Al-Gazali, L I
BARR, D G
Barclay, R P
Barlow, K M
Barr, D G
Belton, N R
Bonthron, D T
Buckton, K E
Burt, A M
Darling, J A
Dixon, P H
Dunlop, N
Forfar, J O
Kelnar, C J
Kirk, J M
Laing, S C
Prader, A
Stirling, H F
Whitfield, M F
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Topics
Abnormalities, Multiple
Adolescent
Adult
Calcium
Child
Child, Preschool
Female
Humans
Infant
Infant, Newborn
Male
Phenotype
Pseudohypoparathyroidism
abnormalities
blood
complications
drug therapy
genetics
metabolism
therapeutic use
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Languages
English
Your search returned 28 results.
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21.
Outcome in tyrosinaemia type II.
[electronic resource]
by
Barr, D G
Kirk, J M
Laing, S C
Producer:
19911223
In:
Archives of disease in childhood
vol. 66
Online resources:
Available from publisher's website
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22.
Parental consanguinity in the blepharophimosis, heart defect, hypothyroidism, mental retardation syndrome (Young-Simpson syndrome).
[electronic resource]
by
Bonthron, D T
Barlow, K M
Burt, A M
Barr, D G
Producer:
19930520
In:
Journal of medical genetics
vol. 30
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23.
Short report: Hyperammonaemia in critically ill septic infants.
[electronic resource]
by
McEwan, P
Simpson, D
Kirk, J M
Barr, D G
McKenzie, K J
Producer:
20010719
In:
Archives of disease in childhood
vol. 84
Online resources:
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24.
Rhizomelic chondrodysplasia punctata with isolated DHAP-AT deficiency.
[electronic resource]
by
Barr, D G
Kirk, J M
al Howasi, M
Wanders, R J
Schutgens, R B
Producer:
19930504
In:
Archives of disease in childhood
vol. 68
Online resources:
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25.
Chronic hypoparathyroidism in two generations.
[electronic resource]
by
Barr, D G
Prader, A
Esper, U
Rampini, S
Marrian, V J
Forfar, J O
Producer:
19720528
In:
Helvetica paediatrica acta
vol. 26
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26.
Organisation of the human PAX4 gene and its exclusion as a candidate for the Wolcott-Rallison syndrome.
[electronic resource]
by
Bonthron, D T
Dunlop, N
Barr, D G
El Sanousi, A A
Al-Gazali, L I
Producer:
19980630
In:
Journal of medical genetics
vol. 35
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27.
Neurogenic chronic idiopathic intestinal pseudo-obstruction, patent ductus arteriosus, and thrombocytopenia segregating as an X linked recessive disorder.
[electronic resource]
by
FitzPatrick, D R
Strain, L
Thomas, A E
Barr, D G
Todd, A
Smith, N M
Scobie, W G
Producer:
19971006
In:
Journal of medical genetics
vol. 34
Online resources:
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28.
GNAS1 mutational analysis in pseudohypoparathyroidism.
[electronic resource]
by
Ahmed, S F
Dixon, P H
Bonthron, D T
Stirling, H F
Barr, D G
Kelnar, C J
Thakker, R V
Producer:
19990111
In:
Clinical endocrinology
vol. 49
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