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C12. Male Urogenital Diseases |
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C13. Female Urogenital Diseases and Pregnancy Complications (group results) |
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C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities: all > Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] > Congenital Abnormalities [MESH:D000013] > Nervous System Malformations [MESH:D009421] > Hereditary Sensory and Motor Neuropathy [MESH:D015417] > Charcot-Marie-Tooth Disease [MESH:D002607] (group results) |
Charcot-Marie-Tooth Disease, Axonal, Type 2a1 [MESH:C566138] (53)
Charcot-Marie-Tooth Disease, Axonal, Type 2A2 [MESH:C563757] (29)
Charcot-Marie-Tooth Disease, Axonal, Type 2n [MESH:C567653] (32)
Charcot-Marie-Tooth Disease, Demyelinating, Type 1e [MESH:C566136] (74)
Charcot-Marie-Tooth Disease, Dominant Intermediate B [MESH:C564703] (26)
Charcot-Marie-Tooth Disease, Dominant Intermediate C [MESH:C564257] (38)
Charcot-Marie-Tooth Disease, Dominant Intermediate D [MESH:C564333] (20)
Charcot-Marie-Tooth Disease, Recessive Intermediate A [MESH:C564256] (13)
Charcot-Marie-Tooth disease, Type 1C [MESH:C537984] (68)
Charcot-Marie-Tooth disease, Type 1D [MESH:C537985] (104)
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C17. Skin and Connective Tissue Diseases: all > Connective Tissue Diseases [MESH:D003240] (group results) |
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D06. Hormones, Hormone Substitutes, and Hormone Antagonists (group results) |
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E. Analytical, Diagnostic and Therapeutic Techniques and Equipment (group results) |
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I. Anthropology, Education, Sociology and Social Phenomena |
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C17. Skin and Connective Tissue Diseases: Connective Tissue Diseases [MESH:D003240] |
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Z. Exceptions (4) |
MESH:C014024
| 2,4,5,2',4',5'-hexachlorobiphenyl C014024 | | | | | | | |
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MESH:C029790
| 2,2',3',4,4',5-hexachlorobiphenyl C029790 | | | | | | | |
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MESH:D004054
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MESH:D009532
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