Found: 14
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Allelic variations in the human growth hormone-1 gene promoter of growth hormone-deficient patients and normal controls.
- Published in:
- European Journal of Endocrinology, 1997, v. 137, n. 5, p. 474, doi. 10.1530/eje.0.1370474
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- Publication type:
- Article
Opportunity for verbalization does not improve visual change detection performance: A state-trace analysis.
- Published in:
- Behavior Research Methods, 2017, v. 49, n. 3, p. 853, doi. 10.3758/s13428-016-0741-1
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- Publication type:
- Article
An R package for state-trace analysis.
- Published in:
- Behavior Research Methods, 2012, v. 44, n. 3, p. 644, doi. 10.3758/s13428-012-0232-y
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- Publication type:
- Article
An Exon Splice Enhancer Mutation Causes Autosomal Dominant GH Deficiency.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2002, v. 87, n. 2, p. 847, doi. 10.1210/jcem.87.2.8236
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- Publication type:
- Article
Familial Dwarfism due to a Novel Mutation of the Growth Hormone-Releasing Hormone Receptor Gene.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 1999, v. 84, n. 3, p. 917, doi. 10.1210/jcem.84.3.5599
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- Publication type:
- Article
The effect of perceptual information on output interference.
- Published in:
- Psychonomic Bulletin & Review, 2019, v. 26, n. 1, p. 269, doi. 10.3758/s13423-018-1521-y
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- Publication type:
- Article
Dynamic memory searches: Selective output interference for the memory of facts.
- Published in:
- Psychonomic Bulletin & Review, 2015, v. 22, n. 6, p. 1798, doi. 10.3758/s13423-015-0840-5
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- Publication type:
- Article
High frequency of BMPR2 exonic deletions/duplications in familial pulmonary arterial hypertension.
- Published in:
- 2006
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- Publication type:
- journal article
High Frequency of BMPR2 Exonic Deletions/Duplications in Familial Pulmonary Arterial Hypertension.
- Published in:
- American Journal of Respiratory & Critical Care Medicine, 2006, v. 174, n. 5, p. 590, doi. 10.1164/rccm.200602-165OC
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- Publication type:
- Article
Serotonin Transporter Polymorphisms in Familial and Idiopathic Pulmonary Arterial Hypertension.
- Published in:
- American Journal of Respiratory & Critical Care Medicine, 2006, v. 173, n. 7, p. 798, doi. 10.1164/rccm.200509-1361OC
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- Publication type:
- Article
Pulmonary Veno-occlusive Disease Caused by an Inherited Mutation in Bone Morphogenetic Protein Receptor II.
- Published in:
- American Journal of Respiratory & Critical Care Medicine, 2003, v. 167, n. 6, p. 889, doi. 10.1164/rccm.200208-861OC
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- Publication type:
- Article
Multilocus Analysis of Hypertension: A Hierarchical Approach.
- Published in:
- Human Heredity, 2004, v. 57, n. 1, p. 28, doi. 10.1159/000077387
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- Publication type:
- Article
Isolated growth hormone (GH) deficiency due to compound heterozygosity for two new mutations in the GH-releasing hormone receptor gene.
- Published in:
- Clinical Endocrinology, 2001, v. 54, n. 5, p. 681, doi. 10.1046/j.1365-2265.2001.01273.x
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- Publication type:
- Article
A Novel Mechanism of Aberrant Pre-mRNA Splicing in Humans.
- Published in:
- Human Molecular Genetics, 1997, v. 6, n. 6, p. 909, doi. 10.1093/hmg/6.6.909
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- Publication type:
- Article