Pesquisas alternativas:
carlos patino » carlos patricio (Expandir a Pesquisa), carlos pardo (Expandir a Pesquisa)
chan carlos » juan carlos (Expandir a Pesquisa), jean carlos (Expandir a Pesquisa), san carlos (Expandir a Pesquisa)
gli complex » gi complex (Expandir a Pesquisa), gdi complex (Expandir a Pesquisa), gpi complex (Expandir a Pesquisa)
comer can » omer can (Expandir a Pesquisa), comer dan (Expandir a Pesquisa), comes can (Expandir a Pesquisa)
can newts » can new (Expandir a Pesquisa), can newly (Expandir a Pesquisa)
case non » cause non (Expandir a Pesquisa), case note (Expandir a Pesquisa), use non (Expandir a Pesquisa)
oil chan » oil can (Expandir a Pesquisa), gil chan (Expandir a Pesquisa), oil than (Expandir a Pesquisa)
l comer » al comer (Expandir a Pesquisa), el comer (Expandir a Pesquisa), all comer (Expandir a Pesquisa)
_ gli » _ glia (Expandir a Pesquisa), _ glp (Expandir a Pesquisa), _ glu (Expandir a Pesquisa)
l oil » _ oil (Expandir a Pesquisa)
A mostrar 1 - 20 resultados de 30 para a pesquisa '(( j l comer can newts ) OR ((( _ gli complex case non ) OR ( l oil chan carlos patino ))))*', tempo de pesquisa: 1.86seg Refinar resultados
A novel GLI3 mutation affecting the zinc finger domain leads to preaxial-postaxial polydactyly-syndactyly complex
Non-canonical Hedgehog Signaling Pathway in Cancer: Activation of GLI Transcription Factors Beyond Smoothened

A recessive homozygous p.Asp92Gly SDHD mutation causes prenatal cardiomyopathy and a severe mitochondrial complex II deficiency
Polycystic kidney and hepatic disease 1 gene mutations in von Meyenburg complexes: Case report

Complex medical history of a patient with a compound heterozygous mutation in C1QC
Relationship between ADD1 Gly460Trp gene polymorphism and essential hypertension in Madeira Island

Local amino acid sequence patterns dominate the heterogeneous phenotype for the collagen connective tissue disease Osteogenesis Imperfecta resulting from Gly mutations
Significant association of rare variant p.Gly8Ser in cardiac sodium channel β4-subunit SCN4B with atrial fibrillation

Structural changes in DNA-binding proteins on complexation
Genotype-phenotype correlations of TGFBI p.Leu509Pro, p.Leu509Arg, p.Val613Gly, and the allelic association of p.Met502Val-p.Arg555Gln mutations

Rare Functional Variants in Genome–wide Association Identified Candidate Genes for Non-syndromic Clefts in the African Population
The Effectiveness of Afatinib in a Patient with Advanced Lung Adenocarcinoma Harboring Rare G719X and S768I Mutations

A malignant pheochromocytoma in a child with von Hippel-Lindau mutation
A210 NEONATAL INFLAMMATORY SKIN AND BOWEL DISEASE CAUSED BY A HOMOZYGOUS EGFR MUTATION: A CASE REPORT AND REVIEW OF THE MEDICAL LITERATURE.

MON-472 Potentially Pathogenic Variants Identified in Patients with Hypopituitarism by Molecular Inversion Probe Sequencing (MIPS), a New Molecular Approach for Low Cost Gene Panel Sequencing
Exact and Effective Pair-Wise Potential for Protein-Ligand Interactions Obtained from a Semiempirical Energy Partition

La Mostra d’Oltremare nella Napoli occidentale
Dietro al microfono. Intellettuali italiani alla Radio svizzera (1930-1980)

The “Essential Practice of Religion” Doctrine in India and its application in Pakistan and Malaysia
Molecular Defects in the Motor Adaptor BICD2 Cause Proximal Spinal Muscular Atrophy with Autosomal-Dominant Inheritance

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