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Differential diagnosis of Smith-Magenis syndrome: 1p36 deletion syndrome

Greenwood Genetic Center; Universidade Estadual Paulista (Unesp); Universidade do Estado do Rio de Janeiro (UERJ); Clemson University (2011-05-01)

Differential diagnosis of Smith-Magenis syndrome: 1p36 deletion syndrome

Greenwood Genetic Center; Universidade Estadual Paulista (Unesp); Universidade do Estado do Rio de Janeiro (UERJ); Clemson University (2011-05-01)

Angiotensin-converting enzyme and apolipoproteins genes polymorphism in coronary artery disease

Mansur, AP; Annicchino-Bizzacchi, J; Favarato, D; Avakian, SD; Cesar, LAM; Ramires, JAF (Clinical Cardiology Publ CoMahwahEUA, 2000)

[polymorphisms Gstm1 And Gstt1 And Sporadic Breast Cancer Mammographic Features].

Morais, Lívia Martins Tavares Scianni; Cardoso Filho, Cássio; Lourenço, Gustavo Jacob; Shinzato, Julia Yoriko; Zeferino, Luiz Carlos; Lima, Carmen Sílvia Passos; Gurgel, Maria Salete Costa ()

Deletion 22q11.2: Report of a complex meiotic mechanism of origin

Belangero, Sintia Iole [UNIFESP]; Hacker, April M.; Bellucco, Fernanda T. S.; Kulikowski, Leslie Domenici; Christofolini, Denise Maria; Cernach, Mirlene C.; Melaragno, Maria Isabel; Emanuel, Beverly S. (Wiley-Blackwell, 2007-08-01)

We report on the case of a patient with a typical de novo 3 Mb 22q11.2 deletion. Haplotype reconstruction of the family, using polymorphic markets flanking the deleted region, demonstrated a complex mechanism of origin of ...

Channel Glass-based Detection of Human Short Insertion/ Deletion Polymorphisms by Tandem Hybridization

Betanzos Cabrera, Gabriel (2008)

The development and critical evaluation of newtechnologies for identifying genetic polymorphisms willrapidly accelerate the discovery and diagnosis of diseaserelatedgenes. We report a novel way for distinguishing anew class ...

Angiotensin converting enzyme polymorphism in type 2 diabetes mellitus

Universidade Estadual Paulista (Unesp) (2014)

This study was undertaken to assess the frequency of angiotensin converting enzyme (ACE) insertion/deletion (I/D) polymorphism in patients with type 2 diabetes mellitus. A total of 162 patients with type 2 diabetes and 160 ...

Effect of hypertension on angiotensin-(1-7) levels in rats with different angiotensin-I converting enzyme polymorphism

Ocaranza, MP; Palomera, C; Roman, M; Bargetto, J; Lavandero, S; Jalil, JE (PERGAMON-ELSEVIER SCIENCE LTD, 2006)

To determine circulating angiotensin-(1-7) [Ang-(1,7)] levels in rats with different angiotensin converting enzyme (ACE) genotypes and to evaluate the effect of hypertension on levels of this heptapeptide, plasma levels ...

Chimerism Interpretation With A Highly Sensitive Quantitative Pcr Method: 6 Months Median Latency Before Chimerism Drop Below 0.1%

Vicente; DC; Laranjeira; ABA; Miranda; ECM; Yunes; JA; de Souza; CA (NATURE PUBLISHING GROUPLONDON, 2016)

Chimerism Interpretation With A Highly Sensitive Quantitative Pcr Method: 6 Months Median Latency Before Chimerism Drop Below 0.1%

Vicente; D. C.; Laranjeira; A. B. A.; Miranda; E. C. M.; Yunes; J. A.; de Souza; C. A. (Nature Publishing GroupLondon, 2016)

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Differential diagnosis of Smith-Magenis syndrome: 1p36 deletion syndrome

Differential diagnosis of Smith-Magenis syndrome: 1p36 deletion syndrome

Angiotensin-converting enzyme and apolipoproteins genes polymorphism in coronary artery disease

[polymorphisms Gstm1 And Gstt1 And Sporadic Breast Cancer Mammographic Features].

Deletion 22q11.2: Report of a complex meiotic mechanism of origin

Channel Glass-based Detection of Human Short Insertion/ Deletion Polymorphisms by Tandem Hybridization

Angiotensin converting enzyme polymorphism in type 2 diabetes mellitus

Effect of hypertension on angiotensin-(1-7) levels in rats with different angiotensin-I converting enzyme polymorphism

Chimerism Interpretation With A Highly Sensitive Quantitative Pcr Method: 6 Months Median Latency Before Chimerism Drop Below 0.1%

Chimerism Interpretation With A Highly Sensitive Quantitative Pcr Method: 6 Months Median Latency Before Chimerism Drop Below 0.1%