(Q47636478)

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Maternal serum screening abnormality in a fetus associated with arthrogryposis multiplex congenita and amyoplasia

scientific article published in December 1997

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Europe PubMed Central

PubMed publication ID

9467818

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4 February 2018

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http://europepmc.org/abstract/MED/9467818

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Maternal serum screening abnormality in a fetus associated with arthrogryposis multiplex congenita and amyoplasia (English)

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Europe PubMed Central

PubMed publication ID

9467818

retrieved

4 February 2018

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http://europepmc.org/abstract/MED/9467818

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Chen CP

1

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Europe PubMed Central

PubMed publication ID

9467818

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4 February 2018

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http://europepmc.org/abstract/MED/9467818

Lin SP

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2

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Europe PubMed Central

PubMed publication ID

9467818

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4 February 2018

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http://europepmc.org/abstract/MED/9467818

publication date

1 December 1997

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9467818

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4 February 2018

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http://europepmc.org/abstract/MED/9467818

published in

Prenatal Diagnosis

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9467818

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4 February 2018

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http://europepmc.org/abstract/MED/9467818

volume

17

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Europe PubMed Central

PubMed publication ID

9467818

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4 February 2018

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http://europepmc.org/abstract/MED/9467818

issue

12

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Europe PubMed Central

PubMed publication ID

9467818

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4 February 2018

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http://europepmc.org/abstract/MED/9467818

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1187-1188

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Europe PubMed Central

PubMed publication ID

9467818

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4 February 2018

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cites work

Sonographic and maternal serum screening abnormalities in fetuses affected by spinal muscular atrophy

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https://api.crossref.org/works/10.1002%2F%28SICI%291097-0223%28199712%2917%3A12%3C1187%3A%3AAID-PD203%3E3.0.CO%3B2-A

retrieved

21 January 2018

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DOI

10.1002/(SICI)1097-0223(199712)17:12<1187::AID-PD203>3.0.CO;2-A

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9467818

retrieved

4 February 2018

reference URL

http://europepmc.org/abstract/MED/9467818

PubMed publication ID

9467818

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9467818

retrieved

4 February 2018

reference URL

http://europepmc.org/abstract/MED/9467818

(Q47636478)

Maternal serum screening abnormality in a fetus associated with arthrogryposis multiplex congenita and amyoplasia

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