Resultados de procura - Collins, Julianne S

Detecting Polymorphisms and Mutations in Candidate Genes por Collins, Julianne S., Schwartz, Charles E.

Ligazón do recurso Ligazón do recurso

Detailed Assessment of the Ear in Cornelia de Lange Syndrome: Comparison with a Control Sample Using the New Dysmorphology Guidelines por Hunter, Alasdair GW, Collins, Julianne S, Deardorff, Matthew A, Krantz, Ian D

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Bootstrap calibration of TRANSMIT for informative missingness of parental genotype data por Allen, Andrew S, Collins, Julianne S, Rathouz, Paul J, Selander, Craig L, Satten, Glen A

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Effect of population stratification on the identification of significant single-nucleotide polymorphisms in genome-wide association studies por Sarasua, Sara M, Collins, Julianne S, Williamson, Dhelia M, Satten, Glen A, Allen, Andrew S

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Long Term Maintenance of Neural Tube Defects Prevention in a High Prevalence State por Collins, Julianne S., Atkinson, Kristy K., Dean, Jane H., Best, Robert G., Stevenson, Roger E.

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Evidence that SIZN1 is a Candidate X-Linked Mental Retardation Gene por Cho, Ginam, Bhat, Shambhu S, Gao, Jinsong, Collins, Julianne S, Rogers, R. Curtis, Simensen, Richard J, Schwartz, Charles E, Golden, Jeffrey A, Srivastava, Anand K

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Prevalence of SHANK3 variants in patients with different subtypes of autism spectrum disorders por Boccuto, Luigi, Lauri, Maria, Sarasua, Sara M, Skinner, Cindy D, Buccella, Daniela, Dwivedi, Alka, Orteschi, Daniela, Collins, Julianne S, Zollino, Marcella, Visconti, Paola, DuPont, Barb, Tiziano, Danilo, Schroer, Richard J, Neri, Giovanni, Stevenson, Roger E, Gurrieri, Fiorella, Schwartz, Charles E

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