DNA diagnosis of hydatidiform mole using the polymerase chain reaction

Human Genetics

Volumn 87, Issue 2, 1991, Pages 216-218

  Fukuyama, Ryuichi ^a   Takata, Mizuho ^a   Kudoh, Jun ^a   Sakai, Kosuke ^a   Tamura, Shozo ^b   Shimizu, Nobuyoshi ^a  

^a KEIO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

PRIMER DNA;

ARTICLE; CLINICAL ARTICLE; DNA PROBE; HUMAN; HUMAN TISSUE; HYDATIDIFORM MOLE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL;

ALLELES; BASE SEQUENCE; ELECTROPHORESIS, POLYACRYLAMIDE GEL; FEMALE; HUMAN; HYDATIDIFORM MOLE; MOLECULAR SEQUENCE DATA; POLYMERASE CHAIN REACTION; PREGNANCY; UTERINE NEOPLASMS;

EID: 0025737317     PISSN: 03406717     EISSN: 14321203     Source Type: Journal    
DOI: 10.1007/BF00204186     Document Type: Article

References (15)

1. Rapid typing of tandemly repeated hypervariable loci by the polymerase chain reaction: application to the apolipoprotein B 3′ hypervariable region
2. Two patients with complete hydatidiform mole with 46, XY karyotype
3. Frequency of heterozygous complete hydatidiform moles, estimated by locus-specific minisatellite and Y chromosome-specific probes
4. Androgenetic origin of hydatidiform mole
5. An improved method for prenatal diagnosis of genetic diseases by analysis of amplified DNA sequence. Application to hemophilia A
6. Genetic aspects of gestational trophoblastic tumors
7. Death from pulmonary embolism associated with hydatidiform mole
8. Benign pulmonary metastasis from hydatidiform mole. Report case
9. Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase
10. Complete and partial hydatidiform moles: cytogenetic and morphological aspects
11. Acute pulmonary complications of molar pregnancy
12. The polymerase chain reaction: an improved method for the analysis of nucleic acids
13. Malignant potential of homozygous and heterozygous complete moles
14. Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy
15. Direct gene analysis of chorionic villi: a possible technique for first-trimester antenatal diagnosis of haemoglobinopathies