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Volumn 19, Issue 7-8, 2003, Pages 440-443
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Molecular genetics of central nervous system malformations
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Author keywords
Central nervous system; Genetic diorders; In utero sampling procedures; Prenatal diagnosis
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Indexed keywords
1 ALKYL 2 ACETYLGLYCEROPHOSPHOCHOLINE ESTERASE;
CELL ADHESION MOLECULE;
GENE PRODUCT;
PROTEIN EMX2;
SONIC HEDGEHOG PROTEIN;
TRANSCRIPTION FACTOR;
UNCLASSIFIED DRUG;
AGYRIA;
AMNIOCENTESIS;
ARTICLE;
CENTRAL NERVOUS SYSTEM MALFORMATION;
DIAGNOSTIC ACCURACY;
DISEASE SEVERITY;
FETUS;
GENE MUTATION;
GENETIC ASSOCIATION;
GENETIC REGULATION;
HOLOPROSENCEPHALY;
HUMAN;
HYDROCEPHALUS;
KARYOTYPING;
MOLECULAR GENETICS;
NERVOUS SYSTEM DEVELOPMENT;
PATHOGENESIS;
PRENATAL DIAGNOSIS;
PRIORITY JOURNAL;
SCHIZENCEPHALY;
AMNIOCENTESIS;
AMNIOTIC FLUID;
CENTRAL NERVOUS SYSTEM;
CHORIONIC VILLI;
CYTOGENETICS;
DNA MUTATIONAL ANALYSIS;
FAMILY HEALTH;
FEMALE;
FETUS;
GESTATIONAL AGE;
HUMANS;
MUTATION;
NERVOUS SYSTEM MALFORMATIONS;
PREGNANCY;
PRENATAL DIAGNOSIS;
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EID: 0141855240
PISSN: 02567040
EISSN: None
Source Type: Journal
DOI: 10.1007/s00381-003-0785-2 Document Type: Article |
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Times cited : (3)
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References (0)
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