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Pallister-Killian syndrome in a Mexican mestizo patient. Case report
Pallister-Killian Syndrome [I(12p)]: First Pre-Natal Diagnosis Using Cordocentesis In The Second Trimester Confirmed By In Situ Hybridization.
Pallister-Killian syndrome: clinical, cytogenetic and molecular findings in 15 cases.
Partial Trisomy 8q And Partial Monosomy 15q Associated With Congenital Hydrocephalus, Diaphragmatic Hernia, Urinary Tract Anomalies, Congenital Heart Defect And Kyphoscoliosis.
Pentalogy of Cantrell: Case Report With Review of the Literature
Prevalence of selected congenital anomalies in the Czech Republic
Pulmonary Agenesis,
Pulmonary Agenesis, Microphthalmia, And Diaphragmatic Defect (PMD): New Syndrome Or Association?
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