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Volumn 18, Issue 2, 1998, Pages 169-172
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Prenatal diagnosis of Charcot-Marie-Tooth disease
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Author keywords
[No Author keywords available]
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Indexed keywords
CELL NUCLEUS DNA;
CONNEXIN 32;
MYELIN PROTEIN;
AMNION CELL;
CHROMOSOME 17P;
FEMALE;
FLUORESCENCE IN SITU HYBRIDIZATION;
GENE LOCUS;
GENE MAPPING;
GENE MUTATION;
HEREDITARY MOTOR SENSORY NEUROPATHY;
HUMAN;
NERVE CONDUCTION;
POLYMERASE CHAIN REACTION;
PRENATAL DIAGNOSIS;
PRIORITY JOURNAL;
PULSED FIELD GEL ELECTROPHORESIS;
SHORT SURVEY;
CHARCOT-MARIE-TOOTH DISEASE;
FEMALE;
HUMANS;
IN SITU HYBRIDIZATION, FLUORESCENCE;
MULTIGENE FAMILY;
MUTATION;
PREGNANCY;
PRENATAL DIAGNOSIS;
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EID: 0031908908
PISSN: 01973851
EISSN: None
Source Type: Journal
DOI: 10.1002/(SICI)1097-0223(199802)18:2<169::AID-PD287>3.0.CO;2-1 Document Type: Short Survey |
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Times cited : (9)
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References (16)
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