Method for detecting chromosome deficiencies for congenital abnormality

Provided is a method for detecting diseases involving multiple anomalads accompanying mental retardation by analyzing the presence or absence of amplification or deficiency in the human chromosome to clarify the causes of the diseases. The method detects the multiple anomalads accompanying the menta...

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Hauptverfasser:	HAYASHI SHIN, INAZAWA JOHJI, AIZU YOSHINORI, IMOTO ISSEI
Format:	Patent
Sprache:	chi ; eng
Schlagworte:	BEER BIOCHEMISTRY CHEMISTRY COMPOSITIONS OR TEST PAPERS THEREFOR COMPOSITIONS THEREOF CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL ORENZYMOLOGICAL PROCESSES CULTURE MEDIA ENZYMOLOGY INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIRCHEMICAL OR PHYSICAL PROPERTIES MEASURING MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEICACIDS OR MICROORGANISMS METALLURGY MICROBIOLOGY MICROORGANISMS OR ENZYMES MUTATION OR GENETIC ENGINEERING PHYSICS PROCESSES OF PREPARING SUCH COMPOSITIONS PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS SPIRITS TESTING VINEGAR WINE
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Beschreibung
Zusammenfassung:	Provided is a method for detecting diseases involving multiple anomalads accompanying mental retardation by analyzing the presence or absence of amplification or deficiency in the human chromosome to clarify the causes of the diseases. The method detects the multiple anomalads accompanying the mental retardation by detecting a hemizygote deficiency in the region of 10q24.31 to 10q25.1 of the human chromosome. The method is suitably performed by detecting a signal that is generated by hybridization between nucleic acid including a part of the region of 10q24.31 to 10q25.1 and a nucleic acid specimen on the basis of the hemizygote deficiency.