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Scholar Results 1 - 10 of about 101 related to SHAPIRO: New frontiers in genetic medicine. (0.09 sec) 

New frontiers in genetic medicine


LJ SHAPIRO, DE COMINGS, OW JONES, DL … - Annals of internal medicine, 1986 - Am Coll Physicians
Disorders determined wholly or in part by genetic factors constitute a
substantial number of human diseases. This realization has grown during the past
2 decades with the recognition of many specific heritable conditions and ...
Cited by 4 - Related articles - All 3 versions

The physician and the rights of mankind


PJ Paul… - JAMA, 1984 - Am Med Assoc
AT THE close of the 35th General Assembly of the World Medical Association in
Venice you proposed to come to Rome to meet with me. You are cordially welcomed
here in this house, so much the more since there exists a special affinity ...
Cited by 1 - Related articles

[CITATION] Recombinant DNA and the clinics.


RF Pettersson - Annals of clinical research, 1986 - ncbi.nlm.nih.gov
1: Ann Clin Res. 1986;18(5-6):217-9. Recombinant DNA and the clinics. Pettersson
RF. Mesh Terms: Chromosome Mapping; Cloning, Molecular ...
Cited by 1 - Related articles

Myotonic muscular dystrophy: From clinical description to molecular genetics


AD Roses - Archives of Internal Medicine, 1985 - archinte.highwire.org
Myotonic muscular dystrophy (DM) is the most prevalent of the human muscular
dystrophies. The disease is inherited as an autosomal dominant trait and is
charac- terized by variable penetrance and variable expressivity. Many ...
Cited by 1 - Related articles - All 4 versions

[CITATION] Achondroplasia due to DNA insertion into the type II collagen gene


СM Strom - Pediatr. Res, 1984
Cited by 2 - Related articles

[CITATION] Towards gene therapy for adenosine deaminase deficiency.


JW Belmont, J Henkel-Tigges, K Wager- … - Annals of clinical research, 1986 - ncbi.nlm.nih.gov
1: Ann Clin Res. 1986;18(5-6):322-6. Towards gene therapy for adenosine deaminase
deficiency. Belmont JW, Henkel-Tigges J, Wager-Smith K, Chang SM, Caskey CT. ...
Cited by 2 - Related articles

Direct alteration of a gene in the human genome


O Smithies - Journal of Inherited Metabolic Disease, 1986 - Springer
Direct alteration of a gene in the human genome requires an understanding of the
role of the gene in metabolism. A gene may need to be introduced into a specific
tissue or alternatively it may be possible to use accessible tissue such as ...
Cited by 3 - Related articles - All 2 versions

[CITATION] Cardiomyopathy associated with neuromuscular disorders


JR Moorman, AD Roses - Cardiomyopathy. Littleton, Mass, PSG Publishing Co, 1988
Cited by 2 - Related articles

[CITATION] Molecular genetic approaches to the analysis of inherited neurological disease.


DN Cooper - Annals of clinical research, 1986 - ncbi.nlm.nih.gov
1: Ann Clin Res. 1986;18(5-6):264-70. Molecular genetic approaches to the
analysis of inherited neurological disease. Cooper DN. ...
Cited by 2 - Related articles

Molecular genetics, basal ganglia disorders, and the clinical neurologist.


R Eldridge - Neurologic clinics, 1984 - ncbi.nlm.nih.gov
The emphasis of this article is on gene mapping, clinical neurogenetics, genetic
factors in common disease, and classification of the hereditary disorders of the
basal ganglia. This was influenced by the recent assignment for the ...
Cited by 2 - Related articles


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