Suchergebnisse - "Linhares, Natália D"

PubPharm (12)

1

Letter by Linhares et al Regarding Article, "Cardiomyopathy and Preeclampsia : Shared Genetics?"

enthalten in: Circulation | 2019

von Linhares, N. | Conceição, I. | Luizon, M.

CommentOn: Circulation. 2018 Nov 20;138(21):2359-2366. - PMID 30021846

2

Genetic deletion of the alamandine receptor MRGD leads to dilated cardiomyopathy in mice

enthalten in: American journal of physiology. Heart and circulatory physiology | 2019

von Oliveira, A. | Melo, M. | Motta-Santos, D. | +16

3

X chromosome dosage and presence of SRY shape sex-specific differences in DNA methylation at an autosomal region in human cells

enthalten in: Biology of sex differences | 2018

von Ho, B. | Greenlaw, K. | Al Tuwaijri, A. | +13

4

X chromosome dosage and presence of SRY shape sex-specific differences in DNA methylation at an autosomal region in human cells

enthalten in: Biology of sex differences | 2018

von Ho, B. | Greenlaw, K. | Al Tuwaijri, A. | +13

5

X chromosome dosage and presence of SRY shape sex-specific differences in DNA methylation at an autosomal region in human cells

enthalten in: Biology of sex differences | 2018

von Ho, B. | Greenlaw, K. | Al Tuwaijri, A. | +13

6

"Exome sequencing identifies a novel homozygous variant in NDRG4 in a family with infantile myofibromatosis (Linhares et al., 2014)" turns out to be EBV+ leiomyomatosis caused by CARMIL2 mutations

enthalten in: European journal of medical genetics | 2018

von Linhares, N. | Freire, M. | Cardenas, R. | +3

CommentOn: Eur J Med Genet. 2014 Nov-Dec;57(11-12):643-8. - PMID 25241110

7

Familial STAG2 germline mutation defines a new human cohesinopathy

enthalten in: NPJ genomic medicine | 2017

von Soardi, F. | Machado-Silva, A. | Linhares, N. | +14

8

Inherited Xq13.2-q21.31 duplication in a boy with recurrent seizures and pubertal gynecomastia : Clinical, chromosomal and aCGH characterization

enthalten in: Meta gene | 2016

von Linhares, N. | Valadares, E. | da Costa, S. | +5

9

Subtelomeric 6p25 deletion/duplication : Report of a patient with new clinical findings and genotype-phenotype correlations

enthalten in: European journal of medical genetics | 2015

von Linhares, N. | Svartman, M. | Rodrigues, T. | +2

10

Dental developmental abnormalities in a patient with subtelomeric 7q36 deletion syndrome may confirm a novel role for the SHH gene

enthalten in: Meta gene | 2014

von Linhares, N. | Svartman, M. | Salgado, M. | +4