Prenatal and postnatal findings in five cases of Fryns syndrome

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Neuroimaging Findings in Pediatric Genetic Skeletal Disorders: A Review.Fryns Syndrome Associated with Recessive Mutations in PIGN in two Separate Families.

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Prenatal and postnatal findings in five cases of Fryns syndrome

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wetenschappelijk artikel

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наукова стаття, опублікована в липні 2014

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Prenatal and postnatal findings in five cases of Fryns syndrome

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Prenatal and postnatal findings in five cases of Fryns syndrome

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Prenatal and postnatal findings in five cases of Fryns syndrome

@en

Prenatal and postnatal findings in five cases of Fryns syndrome

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Prenatal and postnatal findings in five cases of Fryns syndrome

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Prenatal and postnatal findings in five cases of Fryns syndrome

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Prenatal and postnatal findings in five cases of Fryns syndrome

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Ernesto Leva

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Fabrizio Ciralli

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Faustina Lalatta

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Giulia Maria Baffero

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Isabella Fabietti

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Maria Francesca Bedeschi

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Roberto Fogliani

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Tommaso Rizzuti

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P2860

Fryns syndrome: a variable MCA syndrome with diaphragmatic defects, coarse face, and distal limb hypoplasia

Fryns syndrome phenotype caused by chromosome microdeletions at 15q26.2 and 8p23.1

Discordant phenotype in monozygotic twins with Fryns syndrome.

The syndrome of diaphragmatic hernia, abnormal face and distal limb anomalies (Fryns syndrome): report of two sibs with further delineation of this multiple congenital anomaly (MCA) syndrome.

Fryns syndrome survivors and neurologic outcome.

Congenital diaphragmatic hernia, coarse facies, and acral hypoplasia: Fryns syndrome.

Fryns syndrome: case report and review of the literature.

Fryns syndrome: a lethal birth defect with variable phenotypic expressions in siblings.

Cardiovascular malformations in Fryns syndrome: is there a pathogenic role for neural crest cells?

Fryns syndrome in children with congenital diaphragmatic hernia.

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1227-1230

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scholarly article

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10.1002/PD.4447

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P478

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Fabio Mosca

Angela Peron

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2014-07-22T00:00:00Z

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24996149

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Prenatal and postnatal findings in five cases of Fryns syndrome

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P2860

P2860

Prenatal and postnatal findings in five cases of Fryns syndrome

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type

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698