DOCUMENT RESOURCES FOR EVERYONE
Documents tagged
Documents A Short Note on Trisomy 13: Patau’s Syndrome and It’s Diagnosis

Corresponding author Greg Atkinson, Department of Genetics, University of Cambridge, United State. Email: atkinson. [email protected]. Citation Atkinson G (2022) A Short Note

Documents Patau Syndrome (Trisomy 13): Autopsy Case

NIHAL KILINCAbstract Background: Patau syndrome has been estimated to occur in 1 in 12.000-29.000 live births, and the risk is increased with advanced maternal age advanced

Documents Alobar holoprosencephaly and Trisomy 13 (Patau syndrome)

Redalyc.Alobar holoprosencephaly and Trisomy 13 (Patau syndrome)São Paulo Dias Costa, Andressa; Schultz, Regina; Rosemberg, Sérgio Alobar holoprosencephaly

Documents Arhinia

Arhinia Patient Information Series – What you should know, what you should ask. What is Arhinia ? Arhinia is an extremely rare problem of the nose. Babies with arhinia

Documents Congenital partial arhinia: a rare malformation of the nose coexisting with holoprosencephaly

Mizanpaj 54-4.inddThe Turkish Journal of Pediatrics 2012; 54: 440-443 Case Report Congenital partial arhinia: a rare malformation of the nose coexisting with holoprosencephaly

Documents Hydranencephaly: cerebral spinal fluid instead of cerebral mantles

Hydranencephaly: cerebral spinal fluid instead of cerebral mantlesREVIEW Open Access Hydranencephaly: cerebral spinal fluid instead of cerebral mantles Piero Pavone1*, Andrea

Documents Absence of the Septum Pellucidum: A Useful Sign in the Diagnosis of Congenital Brain Malformations

David Norman2 This article appears in the November/Decem­ ber 1988 issue of AJNR and the February 1989 issue of AJR, Received October 23, 1987; accepted after re­