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Clinical report
Noonan syndrome: Severe phenotype and PTPN11 mutations
Síndrome de Noonan: fenotipo grave y mutaciones en el gen PTPN11
Pilar Carrasco Salasa,
Corresponding author
, Gertrudis Gómez-Molinab, Páxedes Carreto-Albab, Reyes Granell-Escobarb, Ignacio Vázquez-Ricoa, Antonio León-Justela
a Human Genetics Unit, Juan Ramón Jiménez Hospital, Huelva, Spain
b Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, Juan Ramón Jiménez Hospital, Huelva, Spain
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ISSN: 00257753
Original language: English
The statistics are updated each day
Year/Month Html Pdf Total
2023 March 8 0 8
2021 October 3 0 3
2019 November 1 0 1
2019 September 1 0 1
2019 February 3 6 9
2019 January 2 2 4

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