369 results on '"Higgins, Joseph"'
Search Results
102. A universal design approach for in situ bioremediation developed from multiple project sites
103. PROBLEM SOLVING AND SOCIAL POSITION AMONG EMOTIONALLY DISTURBED BOYS
104. A Nonverbal Learning Disability in a Case of Central Hypoventilation Syndrome without aPHOX2BGene Mutation
105. Temporal and Spatial Mouse Brain Expression of Cereblon, An Ionic Channel Regulator Involved in Human Intelligence
106. Correction of tracking errors without sensory feedback
107. Correction of false moves in pursuit tracking
108. Faculty Opinions recommendation of Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities.
109. Faculty Opinions recommendation of Oligosaccharyltransferase-subunit mutations in nonsyndromic mental retardation.
110. Pharmacologic properties of AG-012986, a pan-cyclin-dependent kinase inhibitor with antitumor efficacy
111. Faculty Opinions recommendation of DRD3 variant and risk of essential tremor.
112. Hybridize and personalize
113. The impact of a genetics education program on physicians’ knowledge and genetic counseling referral patterns
114. Faculty Opinions recommendation of BKCa-Cav channel complexes mediate rapid and localized Ca2+-activated K+ signaling.
115. Faculty Opinions recommendation of Molecular and imaging correlates of the fragile X-associated tremor/ataxia syndrome.
116. Faculty Opinions recommendation of A functional variant of the dopamine D3 receptor is associated with risk and age-at-onset of essential tremor.
117. Faculty Opinions recommendation of A new detection method for ATRX gene mutations using a mismatch-specific endonuclease.
118. Faculty Opinions recommendation of Genetic analysis of the GABRA1 gene in patients with essential tremor.
119. Faculty Opinions recommendation of Expression of human PQBP-1 in Drosophila impairs long-term memory and induces abnormal courtship.
120. X-linked oligophrenic vermian dysgenesis
121. Integrated physical map of the human essential tremor gene region (ETM2) on chromosome 2p24.3‐p24.2
122. State of the art review: Molecular diagnosis of inherited movement disorders. Movement Disorders Society task force on molecular diagnosis
123. Ultrasonography of the Scrotum
124. Genetics in practice
125. Posterior column ataxia and retinitis pigmentosa: A distinct clinical and genetic disorder
126. Psychosocial factors and the onset of genetic diseases: Dominantly inherited Alzheimer's disease and ataxia—A preliminary investigation
127. Cost/Benefit Analysis of Marine Corps Range Scheduling Systems
128. Evidence that a gene for essential tremor maps to chromosome 2p in four families
129. COMPUTED TOMOGRAPHY MANIFESTATIONS OF METASTATIC CARCINOID SYNDROME WITH RADIO-PHARMACEUTICAL RECEPTOR AND PATHOLOGIC CORRELATION
130. Molecular Characterization of Pyruvate Carboxylase Deficiency in Two Consanguineous Families
131. A gene (ETM) for essential tremor maps to chromosome 2p22‐p25
132. Should spinocerebellar ataxia type 5 be called Lincoln ataxia?
133. CT Patterns of Nodular Hepatic and Splenic Sarcoidosis: A Review of the Literature
134. MOLECULAR CHARACTERIZATION OF PYRUVATE CARBOXYLASE (PC) DEFICIENCY IN TWO CONSANGUINEOUS FAMILIES. † 636
135. Lack of mutations in the biotin-binding region of the pyruvate carboxylase (PC) gene in a family with partial PC deficiency
136. Preserved cognitive processes in cerebellar degeneration
137. MRI, Clinical, and Biochemical Features of Partial Pyruvate Carboxylase Deficiency
138. Dysregulation of large-conductance Ca2+-activated K+ channel expression in nonsyndromal mental retardation due to a cereblon p.R419X mutation.
139. A mutation in a novel ATP-dependent Lon protease gene in a kindred with mild mental retardation.
140. State of the art review: Molecular diagnosis of inherited movement disorders. Movement Disorders Society task force on molecular diagnosis.
141. Optimizing tools fine-tune analog
142. Albumin clearance from alveoli: tissue permeation vs. airway displacement.
143. Fibrinogen clearance from alveoli.
144. Neurological Complications of Hemolytic-Uremic Syndrome.
145. Social Effectiveness and Problem-Solving Thinking of Reformatory Inmates.
146. Prospective Evaluation of Patients with Bowel Wall Thickening.
147. An autosomal recessive disorder with posterior column ataxia and retinitis pigmentosa.
148. Control of movement in Parkinson's disease.
149. Localization of Interaction Sites in Multi-Component Transfer Systems: Theorems Derived from Analogues.
150. ANALYSIS OF SEQUENTIAL REACTIONS.
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