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Items: 4

1.

Pattern of congenital anomalies in newborn: a hospital-based study.

El Koumi MA, Al Banna EA, Lebda I.

Pediatr Rep. 2013 Feb 5;5(1):e5. doi: 10.4081/pr.2013.e5. Print 2013 Feb 5.

2.

Prediction, prevention and personalisation of medication for the prenatal period: genetic prenatal tests for both rare and common diseases.

Dundar M, Uzak AS, Erdogan M, Akbarova Y.

EPMA J. 2011 Jun;2(2):181-95. doi: 10.1007/s13167-011-0080-3. Epub 2011 May 6.

3.

Prenatal diagnosis of skeletal dysplasia due to FGFR3 gene mutations: a 9-year experience : prenatal diagnosis in FGFR3 gene.

Trujillo-Tiebas MJ, Fenollar-Cortés M, Lorda-Sánchez I, Díaz-Recasens J, Carrillo Redondo A, Ramos-Corrales C, Ayuso C.

J Assist Reprod Genet. 2009 Aug;26(8):455-60. doi: 10.1007/s10815-009-9339-1. Epub 2009 Sep 30.

4.

Impact of prenatal diagnosis by ultrasound on the prevalence of congenital anomalies at birth in southern France.

Julian-Reynier C, Philip N, Scheiner C, Aurran Y, Chabal F, Maron A, Gombert A, Aymé S.

J Epidemiol Community Health. 1994 Jun;48(3):290-6.

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