Call Number (LC) | Title | Results |
---|---|---|
RB155 .T736 2016eb | Translational Cardiometabolic Genomic Medicine / | 1 |
RB155 .T74 1996 |
The troubled helix : social and psychological implications of the new human genetics / The Troubled Helix : Social and Psychological Implications of the New Human Genetics / |
3 |
RB155 .V53 2012 | Victor McKusick and the development of medical genetics | 1 |
RB155 .W33 1985 | The new genetics and clinical practice / | 1 |
RB155 .W35 1993 | Genetic variation and human disease : principles and evolutionary approaches / | 2 |
RB155 .W48 | Family skeletons / | 1 |
RB155 .W54 1991 | Exons, introns, and talking genes : the science behind the Human Genome Project / | 1 |
RB155 .W75 2007 | ||
RB155 .Y685 2006 | Designer evolution : a transhumanist manifesto / | 1 |
RB155 .Z54 2010 | A statistical approach to genetic epidemiology / | 1 |
RB155 ebook | Genética humana : fundamentos para el estudio de los efectos sociales derivados de los avances en genética humana : monografías / | 1 |
RB155.5 |
Chimeric RNA : methods and protocols / Transports of Delight : an Aromatic Journey in Verse from East to West on the Wings of Perfume. Jews and Genes : the Genetic Future in Contemporary Jewish Thought. Uniparental disomy (UPD) in clinical genetics : a guide for clinicians and patients / Mobilizing mutations : human genetics in the age of patient advocacy / Epstein's inborn errors of development : the molecular basis of clinical disorders of morphogenesis / Genomics of rare diseases understanding rare disease genetics / The power of the gene : the origin and impact of genetic disorders / Analysis of triplet repeat disorders / Clinical trials of genetic therapy with antisense DNA and DNA vectors / A probabilistic model of the genotype/phenotype relationship : does life play the dice? / Alagille Syndrome : Pathogenesis and Clinical Management / Mitochondria as targets for phytochemicals in cancer prevention and therapy Chimerism : a clinical guide / Signs and symptoms of genetic conditions : a handbook / The chromosome 22q11.2 deletion syndrome a multidisciplinary approach to diagnosis and treatment / NF-[kappa]B-related genetic diseases / Nonsense mutation correction in human diseases : an approach for targeted medicine / Von Hippel-Lindau disease : a comprehensive guide to diagnosis, treatment, and management / Rare genetic disorders advancements in diagnosis and treatment / Chimera research : methods and protocols / The genetics of African populations in health and disease / Familial chylomicronemia syndrome : raising awareness of a rare genetic disease / SEX CHROMOSOME ABNORMALITIES AND HUMAN BEHAVIOR : psychological studies. Genetic Privacy : an Evaluation of the Ethical and Legal Landscape / Un nuevo reto para los derechos fundamentales. Critrios clínicos de enfermedades genéticas Noonan Syndrome : characteristics and interventions / Epigenetics and Dermatology. |
29 |
RB155.5 .A4 2009 | Congenital diseases and syndromes an illustrated radiological guide / | 1 |
RB155.5 .A48 2006eb | Alternative splicing and disease | 1 |
RB155.5 .A53 2010 | Analysis of complex disease association studies : a practical guide / | 1 |
RB155.5 .A53 2011 | Analysis of complex disease association studies a practical guide / | 1 |
RB155.5 .B57 1990 | Genome : the story of the most astonishing scientific adventure of our time--the attempt to map all the genes in the human body / | 2 |
RB155.5 .B67 1980 | ||
RB155.5 .B67 1989 | Chromosomal variation in man : a catalog of chromosomal variants and anomalies / | 1 |
RB155.5 .B67 1991 | Chromosomal variation in man : a catalog of chromosomal variants and anomalies / | 1 |