Listing 1 - 10 of 38 | << page >> |
Sort by
|
Choose an application
Choose an application
Choose an application
Over 1200 entries to literature (mostly English-language journal articles). Intended for human cytogeneticists. Sources were Current contents, various genetics journals from 1970 to the present, and Excerpta medica and Index medicus for afew earlier references. Entries arranged under sections titled Structural variations and anomalies, Numerical anomalies, and Chromosomal breakage syndromes. Author, selected syndrome indexes.
Chromosome Aberrations --- Human chromosome abnormalities --- Human chromosomes --- Karyotypes --- bibliography. --- Chromosome Aberrations.
Choose an application
Medical genetics. --- Genetics, Medical. --- Chromosome Aberrations. --- Genetic Diseases, Inborn.
Choose an application
Chromosome aberrations --- Chromosome abnormalities --- Reference books, medical. --- Bibliography. --- Bibliography.
Choose an application
Chemical mutagenesis --- Chromosome aberrations --- Environmental pollution --- Mutagenesis --- Mutation --- Congresses --- Congresses. --- Chemical mutagenesis - Congresses --- Chromosome aberrations - Congresses --- Environmental pollution - Congresses --- Mutagenesis - Congresses --- Mutation - Congresses
Choose an application
Human chromosome abnormalities. --- Human genetics. --- Medical genetics. --- Genetics, Medical. --- Genetics, Medical --- Chromosome aberrations
Choose an application
Chromosome Aberrations --- B-Lymphocytes --- Gene Expression Regulation, Neoplastic --- Metabolism --- Congresses. --- B cells --- Tumors --- Congresses
Choose an application
This important new book provides a useful, easy-to-use guide to the clinical consultation in genetics. It covers the process of diagnosis, investigation, management, and counselling for patients. The authors have used their experience to devise a practical clinical approach to many common genetic referrals, both out-patient and ward-based. The most common Mendelian disorders, chromosomal disorders, congenital anomalies and syndromes are covered. In addition there are chapters on familial cancer and pregnancy-related topics such as fetal anomalies, teratogens, prenatal and pre-implantation diagnosis. The book also provides information on the less common situations, where management is particularly complex, or important genetic concepts are illustrated. Most of the topics fit onto a double-page spread ensuring that the book is an accessible, quick reference for the clinic or hospital consultation. Where available, diagnostic criteria for specific conditions are included as well as contact details for support groups. The book is well-illustrated and has an up-to-date bibliography and glossaries of terms used in genetics and dysmorphology. This accessible book is designed for use by consultants and trainees in clinical genetics, genetic counsellors and paediatricians, particularly those working in paediatric neurology, neonatology or child development.
Chromosome Aberrations --- Genetic Diseases, Inborn --- Genetic Predisposition to Disease --- Genetics, Medical --- Medical genetics
Choose an application
Human chromosome abnormalities --- Human chromosomes --- Chromosome Aberrations --- Chromosome Abnormalities --- Catalogs and collections. --- Catalogs and collections. --- indexes. --- indexes.
Listing 1 - 10 of 38 | << page >> |
Sort by
|