Assessment of copy number variations in 120 patients with Poland syndrome.

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Anaesthesia for chest wall reconstruction in a patient with Poland syndrome: CARE-compliant case report and literature review.

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Assessment of copy number variations in 120 patients with Poland syndrome.

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2016 nî lūn-bûn

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2016年の論文

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2016年論文

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2016年論文

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2016年論文

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2016年论文

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name

Assessment of copy number variations in 120 patients with Poland syndrome.

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Assessment of copy number variations in 120 patients with Poland syndrome.

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Assessment of copy number variations in 120 patients with Poland syndrome.

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Assessment of copy number variations in 120 patients with Poland syndrome.

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Assessment of copy number variations in 120 patients with Poland syndrome.

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Assessment of copy number variations in 120 patients with Poland syndrome.

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P1476

Assessment of copy number variations in 120 patients with Poland syndrome

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Anwar Baban

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Carlotta Maria Vaccari

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Elisa Tassano

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Filippo Senes

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Ilaria Musante

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Margherita Lerone

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Maria Francesca Bedeschi

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Maria Grazia Calevo

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Maria Teresa Divizia

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Maria Victoria Romanini

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P2860

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

Laminin α4 deficient mice exhibit decreased capacity for adipose tissue expansion and weight gain

Involvement of mouse Rev3 in tolerance of endogenous and exogenous DNA damage

Genetic inactivation of the transcription factor TIF-IA leads to nucleolar disruption, cell cycle arrest, and p53-mediated apoptosis

Smooth-muscle contraction without smooth-muscle myosin

Deletion of the laminin alpha4 chain leads to impaired microvessel maturation

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies

CNVs conferring risk of autism or schizophrenia affect cognition in controls

Cytoscape 2.8: new features for data integration and network visualization

Thrombocytopenia-absent radius (TAR) syndrome due to compound inheritance for a 1q21.1 microdeletion and a low-frequency noncoding RBM8A SNP: a new familial case.

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s12881-016-0351-x

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scholarly article

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10.1186/S12881-016-0351-X

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P478

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Simone Bossi

Aldamaria Puliti

Nunzio Catena

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2016-11-25T00:00:00Z

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1011673438

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Assessment of copy number variations in 120 patients with Poland syndrome.

about

P2860

P2860

Assessment of copy number variations in 120 patients with Poland syndrome.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P6179

P698

P932

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P6179

P698

P932