Found: 12
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Genotype-Phenotype Associations in Patients with Severe Hyperinsulinism of Infancy.
- Published in:
- Pediatric & Developmental Pathology, 2007, v. 10, n. 1, p. 25, doi. 10.2350/06-04-0083.1
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- Publication type:
- Article
Aetiology of the Skeletal Dysmorphology Syndrome Campomelic Dysplasia: Expression of the Sox9 Gene during Chondrogenesis in Mouse Embryosa.
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- Annals of the New York Academy of Sciences, 1996, v. 785, n. 1, p. 350, doi. 10.1111/j.1749-6632.1996.tb56306.x
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- Publication type:
- Article
Analysis of the role of Amh and Fra1 in the Sry regulatory pathway.
- Published in:
- Molecular Reproduction & Development, 1996, v. 44, n. 2, p. 153, doi. 10.1002/(SICI)1098-2795(199606)44:2<153::AID-MRD3>3.0.CO;2-M
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- Publication type:
- Article
Sertoli-Leydig Cell Tumor of the Ovary, a Rare Cause of Precocious Puberty in a 12-Month-Old Infant
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- Journal of Clinical Endocrinology & Metabolism, 2002, v. 87, n. 1, p. 49, doi. 10.1210/jcem.87.1.8162
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- Publication type:
- Article
Further evidence of linkage at 7p22 with familial hyperaldosteronism type II
- Published in:
- 2005
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- Publication type:
- Abstract
No association between primary aldosteronism and two CYP11B2 polymorphisms in a well-characterized Australian sample
- Published in:
- 2005
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- Publication type:
- Abstract
Characterization of pilQ, a new gene required for the biogenesis of type 4 fimbriae in Pseudomonas aeruginosa.
- Published in:
- Molecular Microbiology, 1993, v. 9, n. 4, p. 857, doi. 10.1111/j.1365-2958.1993.tb01744.x
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- Publication type:
- Article
Genetic Forms of Primary Aldosteronism.
- Published in:
- High Blood Pressure & Cardiovascular Prevention, 2007, v. 14, n. 2, p. 75, doi. 10.2165/00151642-200714020-00004
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- Publication type:
- Article
Genetic Forms of Primary Aldosteronism.
- Published in:
- High Blood Pressure & Cardiovascular Prevention, 2007, v. 14, n. 2, p. 75, doi. 10.2165/00151642-200714020-00004
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- Publication type:
- Article
No evidence for coding region mutations in the retinoblastoma-associated Kruppel-associated box protein gene ( RBaK) causing familial hyperaldosteronism type II.
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- 2006
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- Publication type:
- Letter
Genomic structure of the human gene for protein kinase A regulatory subunit R1-beta (PRKAR1B) on 7p22: no evidence for mutations in familial hyperaldosteronism type II in a large affected kindred.
- Published in:
- Clinical Endocrinology, 2004, v. 61, n. 6, p. 716, doi. 10.1111/j.1365-2265.2004.02155.x
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- Publication type:
- Article
Combined pituitary hormone deficiency in Australian children: clinical and genetic correlates.
- Published in:
- Clinical Endocrinology, 2003, v. 58, n. 6, p. 785, doi. 10.1046/j.1365-2265.2003.01781.x
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- Publication type:
- Article