902 results on '"Chitty, Lyn S."'
Search Results
102. 34 - Diagnosis and Management of Fetal Skeletal Abnormalities
103. 22 - Noninvasive Prenatal Diagnosis for Single-Gene Disorders
104. Twenty years of progress in the diagnosis and management of foetal urinary tract conditions.
105. International Society for Prenatal Diagnosis Updated Position Statement on the use of genome-wide sequencing for prenatal diagnosis.
106. A new decade, fond farewells and a new era for Prenatal Diagnosis
107. The clinical utility of microarray technologies applied to prenatal cytogenetics in the presence of a normal conventional karyotype: a review of the literature
108. Right or wrong? Looking through the retrospectoscope to analyse predictions made a decade ago in prenatal diagnosis and fetal surgery
109. Congenital Lung Disease
110. Contributors
111. The 2012 Malcolm Ferguson-Smith Young Investigator Award
112. The clinical implementation of non-invasive prenatal diagnosis for single-gene disorders: challenges and progress made
113. Noninvasive prenatal testing: the paradigm is shifting rapidly
114. Safe, accurate, prenatal diagnosis of thanatophoric dysplasia using ultrasound and free fetal DNA
115. Post-mortem apparent resolution of fetal ventriculomegaly: evidence from magnetic resonance imaging
116. Fetal Skeletal Abnormalities
117. Contributors
118. Fetal forearm anomalies: prenatal diagnosis, associations and management strategy
119. CONTRIBUTORS
120. PRENATAL DIAGNOSIS OF FETAL RENAL ABNORMALITIES
121. What's out there for parents? A systematic review of online information about prenatal microarray and exome sequencing.
122. Service users and care providersʼ experiences of tertiary combined fetal medicine clinics
123. Fetal sex determination using cell-free fetal DNA: service usersʼ experiences of and preferences for service delivery
124. The 2011 Malcolm Ferguson-Smith Young Investigator Award
125. Routine testing of fetal D status in RhD- women using cffDNA: Womenʼs preferences and needs: P1-63
126. Will the introduction of non-invasive prenatal diagnosis for Downʼs syndrome influence informed choice?: 9-3
127. Noninvasive prenatal testing for aneuploidy–ready for prime time?
128. The 2010 Malcolm Ferguson-Smith Young Investigator Award
129. Fetal therapy: progress made and lessons learnt
130. Incremental cost of non-invasive prenatal diagnosis versus invasive prenatal diagnosis of fetal sex in England†
131. Early prenatal diagnosis of skeletal anomalies
132. First trimester screening - new directions for antenatal care?
133. Cell-Free DNA in Pediatric Solid Organ Transplantation Using a New Detection Method of Separating Donor-Derived from Recipient Cell-Free DNA
134. The 2019 Malcolm Ferguson‐Smith Young Investigator Award
135. The role of sonographic phenotyping in delivering an efficient noninvasive prenatal diagnosis service forFGFR3‐related skeletal dysplasias
136. Couples experiences of receiving uncertain results following prenatal microarray or exome sequencing: A mixed‐methods systematic review
137. Current controversies in prenatal diagnosis 2: The 59 genes ACMG recommends reporting as secondary findings when sequencing postnatally should be reported when detected on fetal (and parental) sequencing
138. Development and mixed-methods evaluation of an online animation for young people about genome sequencing
139. List of contributors
140. The routine fetal anomaly scan
141. Noninvasive Prenatal Diagnosis for Cystic Fibrosis: Implementation, Uptake, Outcome, and Implications
142. Noninvasive Prenatal Diagnosis of Single-Gene Diseases: The Next Frontier
143. Molecular prenatal diagnosis: the impact of modern technologies
144. The evolution of prenatal diagnosis
145. “The communication and support from the health professional is incredibly important”: A qualitative study exploring the processes and practices that support parental decision‐making about postmortem examination
146. Delivering genome sequencing in clinical practice: an interview study with healthcare professionals involved in the 100 000 Genomes Project
147. Congenital Lung Disease
148. Contributors
149. Cell-free fetal DNA and RNA in maternal blood: implications for safer antenatal testing
150. The challenge of imaging the fetal central nervous system: an aid to prenatal diagnosis, management and prognosis
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