Literature DB >> 23550868

Prenatal diagnosis of Pfeiffer syndrome prior to 20 weeks' gestation.

J L Gómez-Gómez1, A M Fernández-Alonso, I Moreno-Ortega, L Mas-Greño, J Berenguel-Martínez, G Fiol-Ruiz.   

Abstract

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Year:  2013        PMID： 23550868     DOI： 10.3109/01443615.2012.753424

Source DB:  PubMed          Journal:  J Obstet Gynaecol        ISSN： 0144-3615            Impact factor:   1.246


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  3 in total

1.  Ultrasound and MR imaging findings in prenatal diagnosis of craniosynostosis syndromes.

Authors:  Eva I Rubio; Anna Blask; Dorothy I Bulas
Journal:  Pediatr Radiol       Date:  2016-02-25

2.  Prenatal Diagnosis of Pfeiffer Syndrome Patient with FGFR2 C.940-1G>C Variant: A Case Report.

Authors:  Laura Torres-Canchala; Daniela Castaño; Nathalia Silva; Ana María Gómez; Alejandro Victoria; Harry Pachajoa
Journal:  Appl Clin Genet       Date:  2020-08-11

3.  De Novo Heterozygous Mutation in FGFR2 Causing Type II Pfeiffer Syndrome.

Authors:  Rafat Mosalli; Alfia Fatma; Mohammed A Almatrafi; Mayada Mazroua; Bosco Paes
Journal:  Case Rep Genet       Date:  2022-06-28
  3 in total

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