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101. De Novo Heterozygous Mutations in SMC3 Cause a Range of Cornelia de Lange Syndrome-Overlapping Phenotypes

102. Ring chromosome 4 mosaicism coincidence of oligomeganephronia and signs of Seckel syndrome

105. Voice Abnormalities in Short Stature Syndromes

106. Phenotype of patients with peroxisomal disorders subdivided into sixteen complementation groups

107. Isolation of Decidual Lymphocytes From Chorionic Villus Samples: Phenotypic Analysis and Growth in Vitro

108. Clinical Report: Germline Mosaicism in Cornelia de Lange Syndrome

109. Detection of ≥1Mb microdeletions and microduplications in a single cell using custom oligonucleotide arrays

110. NIPBL rearrangements in Cornelia de Lange syndrome: evidence for replicative mechanism and genotype–phenotype correlation

111. HDAC8 mutations in Cornelia de Lange syndrome affect the cohesin acetylation cycle

112. Study of W boson production in PbPb and pp collisions at √sNN=2.76 TeV

113. Causes of death and autopsy findings in a large study cohort of individuals with Cornelia de Lange syndrome and review of the literature

114. Molecular Technologies Open New Clinical Genetic Vistas

115. Science Translational Medicine Podcast: 12 January 2011

117. Growth manifestations in the Brachmann-de Lange syndrome

118. Facial Diagnosis of Mild and Variant CdLS: Insights from a Dysmorphologist Survey

119. De NovoHeterozygous Mutations inSMC3Cause a Range of Cornelia de Lange Syndrome-Overlapping Phenotypes

120. Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies

121. Confirmation of a cryptic unbalanced translocation using whole chromosome fluorescencein situ hybridization

122. A Randomized Comparison of Transcervical and Transabdominal Chorionic-Villus Sampling

123. Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance

124. Placental mosaicism in a case of 46,XY, −22, +t(22;22)(p11;q11) or i(22q) diagnosed at amniocentesis

125. Maternal uniparental disomy of chromosome 16 and body stalk anomaly

126. Noninvasive prenatal diagnosis of fetal aneuploidies and Mendelian disorders: new innovative strategies

128. New X-linked mental retardation disorder with Dandy-Walker malformation, basal ganglia disease, and seizures

129. Prenatal Diagnosis

130. De novo direct Tandem duplication of the short arm of chromosome 7(p21.1-p14.2)

131. Ophthalmologic Findings in the Cornelia de Lange Syndrome

132. Cornelia de Lange syndrome: clinical review, diagnostic and scoring systems, and anticipatory guidance

133. Bromosilane, Iodosilane, and Trisilylamine

136. Psychosocial correlates of pregnant women's attitudes toward prenatal maternal serum screening and invasive diagnostic testing: beyond traditional risk status

137. Dubowitz syndrome in a boy without developmental delay: Further evidence for phenotypic variability

138. Chromosome Rearrangements in Cornelia de Lange Syndrome (CdLS): Report of a der(3)t(3;12)(p25.3;p13.3) in Two Half Sibs With Features of CdLS and Review of Reported CdLS Cases With Chromosome Rearrangements

139. Elevated first-trimester nuchal translucency increases the risk of congenital heart defects

140. Late first-trimester placental disruption and subsequent gestational hypertension/preeclampsia

141. Precocious sister chromatid separation (PSCS) in Cornelia de Lange syndrome

142. Limb defects and chorionic villus sampling

143. Late first-trimester invasive prenatal diagnosis: results of an international randomized trial

144. Role of autophagy genetic variants for the risk of Candida infections

145. Fetal cells and DNA in maternal blood

146. First-trimester screening for trisomies 21 and 18

147. Probing the fetal genome: progress in non-invasive prenatal diagnosis

148. The safety and efficacy of chorionic villus sampling for early prenatal diagnosis of cytogenetic abnormalities

149. Procedural risks versus theology: chorionic villus sampling for Orthodox Jews at less than 8 weeks' gestation

150. Preparation of Metaphase Spreads from Chorionic Villus Samples

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