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Volumn 18, Issue 3, 1998, Pages 287-289
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Prenatal diagnosis of Menkes disease
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Author keywords
[No Author keywords available]
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Indexed keywords
ADENOSINE TRIPHOSPHATASE;
COPPER;
DNA;
AMNIOTIC FLUID CELL;
CHORION VILLUS;
COPPER METABOLISM;
DIAGNOSTIC PROCEDURE;
DNA DETERMINATION;
GENE MUTATION;
HETEROZYGOTE DETECTION;
HIGH RISK PREGNANCY;
HUMAN;
MENKES SYNDROME;
NEUTRON ACTIVATION ANALYSIS;
PRENATAL DIAGNOSIS;
PRIORITY JOURNAL;
SHORT SURVEY;
ADENOSINE TRIPHOSPHATASES;
CARRIER PROTEINS;
CATION TRANSPORT PROTEINS;
FEMALE;
FETAL DISEASES;
HETEROZYGOTE DETECTION;
HUMANS;
MENKES KINKY HAIR SYNDROME;
MUTATION;
PREGNANCY;
PRENATAL DIAGNOSIS;
RECOMBINANT FUSION PROTEINS;
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EID: 0031935585
PISSN: 01973851
EISSN: None
Source Type: Journal
DOI: 10.1002/(SICI)1097-0223(199803)18:3<287::AID-PD352>3.0.CO;2-7 Document Type: Short Survey |
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Times cited : (17)
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References (16)
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