Sequence variants identification at the KCNQ1OT1:TSS differentially Methylated region in isolated omphalocele cases.

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Sequence variants identification at the KCNQ1OT1:TSS differentially Methylated region in isolated omphalocele cases.

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2017 nî lūn-bûn

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2017年の論文

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2017年論文

@yue

2017年論文

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2017年論文

@zh-hk

2017年論文

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2017年論文

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2017年论文

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2017年论文

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Sequence variants identificati ...... in isolated omphalocele cases.

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Sequence variants identificati ...... in isolated omphalocele cases.

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Sequence variants identificati ...... in isolated omphalocele cases.

@en

Sequence variants identificati ...... in isolated omphalocele cases.

@nl

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Sequence variants identificati ...... in isolated omphalocele cases.

@en

Sequence variants identificati ...... in isolated omphalocele cases.

@nl

P1476

Sequence variants identificati ...... in isolated omphalocele cases.

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P2093

Ernesto Leva

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Fabio Mosca

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Faustina Lalatta

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Laura Fontana

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Leda Paganini

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Lidia Pezzani

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Lorena Canazza

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Lorenzo Colombo

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Marco Baccarin

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Maria Francesca Bedeschi

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Beckwith-Wiedemann and IMAGe syndromes: two very different diseases caused by mutations on the same gene

The vascular pathogenesis of gastroschisis: intrauterine interruption of the omphalomesenteric artery.

Clinical risk factors for gastroschisis and omphalocele in humans: a review of the literature.

Syndromes and disorders associated with omphalocele (III): single gene disorders, neural tube defects, diaphragmatic defects and others.

Self-reported maternal cigarette smoke exposure during the periconceptional period and the risk for omphalocoele.

Familial omphalocele: considerations in genetic counseling.

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scholarly article

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10.1186/S12881-017-0470-Z

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Silvia Tabano

Monica Miozzo

M Calvello

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2017-10-18T00:00:00Z

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1092273302

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