9780072325300

Case Studies Workbook to accompany Human Genetics

by
  • ISBN13:

    9780072325300

  • ISBN10:

    0072325305

  • Edition: 2nd
  • Format: Paperback
  • Copyright: 2000-08-25
  • Publisher: MCG (Manual)
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Summary

"Human Genetics, Seventh Edition," is a non-science majors human genetics text that clearly explains what genes are, how they function, how they interact with the environment, and how our understanding of genetics has changed since completion of the human genome project. It is a clear, modern, and exciting book for citizens who will be responsible for evaluating new medical options, new foods, and new technologies in the age of genomics..

Table of Contents

Acrocephalosyndactyly
1(2)
Acute Leukemia
3(2)
Alcoholism
5(2)
Anhidrotic Ectodermal Dysplasia
7(2)
Argininemia
9(2)
Bloom Syndrome
11(2)
Blue Diaper Syndrome
13(2)
BPES Syndrome
15(2)
Carnitine-acylcarnitine Translocase Deficiency
17(2)
Carnosinemia
19(2)
Charcot-Marie-Tooth Disease
21(2)
Chronic Granulomatous Disease
23(2)
Cleft Lip with or without Cleft Palate
25(2)
Combined Factors V and VIII Deficiency
27(2)
Complement Component 2 Deficiency
29(2)
DiGeorge Syndrome
31(2)
Dilated Cardiomyopathy
33(2)
Ehlers-Danlos Syndrome Type IV
35(2)
Enamel Hypoplasia
37(2)
Epidermolysis Bullosa
39(2)
Familial Mental Retardation (ATR-16)
41(2)
Fatal Familial Insomnia
43(2)
Fragile X Syndrome
45(4)
Gonadal Dysgenesis
49(2)
Gyrate Atrophy
51(2)
Hereditary Multiple Exostoses
53(2)
Huntington-Like Disorder
55(2)
Hypoxia-Inducible Factor I
57(2)
Lattice Corneal Dystrophy
59(2)
Leber Optic Atrophy
61(2)
Li-Fraumeni Family Cancer Syndrome
63(2)
Lysinuric Protein Intolerance
65(2)
Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome
67(2)
Menkes Syndrome
69(2)
Multiple Endocrine Neoplasia
71(2)
Multiple Pterygium Syndrome
73(2)
Muscle Chip
75(2)
Muscular Dystrophy
77(2)
Nephrolithiasis
79(2)
Open-Angle Glaucoma
81(2)
OSMED (OtoSpondyloMegaEpiphyseal Dysplasia)
83(2)
Pallister-Killian Syndrome
85(2)
Pelizaeus-Merzbacher Disease
87(2)
Prenatal Diagnosis
89(2)
Prenatal Microarray Screen
91(2)
Pseudohermaphroditism
93(2)
Russell-Silver Syndrome
95(2)
Schneckenbecken Dysplasia
97(2)
Smith-Lemli-Opitz Syndrome (RSH Syndrome)
99(2)
Tangier Disease
101(2)
Tay-Sachs Disease
103(2)
Thrombocytopenia and Absent Radius Syndrome
105(2)
Thyroid Cancer
107(2)
Townes-Brocks Syndrome
109(2)
Turner Syndrome
111(2)
Ulnar-Mammary Syndrome
113(2)
Venous Thrombosis
115(2)
Vestibular Schwannoma
117(2)
Von Hippel-Lindau Disease
119(2)
Von Willebrand Disease
121(2)
Appendix A, The Genetic Code 123(2)
Appendix B, Symbols in Pedigree Construction 125

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