Information technology will profoundly affect how medicine is practised and healthcare delivered. Past attempts to develop an IT strategy in the National Health Service have been plagued by failure and scandals. It is vital to learn from such mistakes, and to this end experts and practitioners report on aspects of IT in the NHS to set a new agenda for the millennium.
OKA M , KATABUCHI H , MUNEMURA M , MIZUMOTO J , MAEYAMA M : An unusual case of male pseudohermaphroditism ... JACOBS PA , BAIKIE AG , COURT BROWN WM , FORREST H , ROY JR , STEARD JSS , LENNOX B : Chromosomal sex in the syndrome of ...
For centuries the Cromptons have had their portraits painted by the Millers. But when Alix Miller accepts a commision from Lee Crompton to paint his portrait, she little suspects that it will change her life.
Tempel , B. L. , Y. N. Jan , and L. Y. Jan. 1988. Cloning of a probable potassium channel gene from mouse brain . Nature . 332 : 837-9 . Tenenholz , T. C. , R. S. Rogowski , J. H. Collins , M. P. Blaustein , and D. J. Weber . 1997 .
1. Deformations and Disruptions2. Teratogenic Agents3. Chromosomal Syndromes: Common and/or Well-Known Syndromes4. Chromosomal Syndromes: Unusual Variants5. Metabolic Disorders6. Syndromes Affecting Bone: The Osteogenesis Imperfectas7. Syndromes Affecting Bone: Chondrodysplasias and Chondrodystrophies8....
Emery and Rimoin's Principles and Practice of Medical Genetics
Genetic testing and screening Current guidelines for genetic testing Suggested criteria for the introduction of genetic tests Current guidelines for genetic screening Criteria for genetic screening Review of current decision - making ...
The book reviews the pathophysiology and genetics of the disorder, discusses recent molecular advances and its impact on diagnostics, and describes management challenges and strategies. The text also touches upon future treatment options.
VCFS is also referred to as Velo Cardio Facial Syndrome, CHARGE Syndrome, Shprintzen Syndrome, DiGeorge Sequence, Pierre Robin Sequence, Potter Sequence.
Presents clinical, biochemical, and genetic information concerning those metabolic anomalies grouped under inborn errors of metabolism.
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