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190 results on '"Rozensztrauch A"'

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154. La«tete Moris».

171. ASPEKTY INTENSYWNEJ TERAPII NOWORODKA Z WRODZONYM ZAROŚNIĘCIEM PRZEŁYKU.

172. Is c.1431-12G>A A common European mutation of SPINK5?report of a patient with Netherton Syndrome

173. URAZ CZASZKOWO-MÓZGOWY U DZIECKA. OPIS PRZYPADKU.

174. PFAPA SYNDROME IN CHILDREN.

183. Establishment of a condition-specific quality-of-life questionnaire for children born with esophageal atresia aged 2–7 across 14 countries

184. The influence of gestational diabetes mellitus on the developing baby

185. Parent's attitude to vaccinations

186. The Role of the Reanalysis of Genetic Test Results in the Diagnosis of Dysmorphic Syndrome Caused by Inherited xq24 Deletion including the UBE2A and CXorf56 Genes.

187. The Impact of Congenital Esophageal Atresia on the Family Functioning.

188. Changing facial features in a child with GAPO syndrome caused by novel mutation in the ANTXR1 gene and uniparental disomy of chromosome 2.

189. The Quality of Life of Polish Children with Cerebral Palsy and the Impact of the Disease on the Family Functioning.

190. Is c.1431-12G>A A common European mutation of SPINK5? report of a patient with Netherton Syndrome.

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