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Q934 °í¾çÀÌ¿ïÀ½ ÁõÈıº Cri-du-chat syndrome
Q935 ¿°»öüÀÇ ±âŸ ºÎºÐ °á¼Õ Other deletions of part of a chromosome
Q935 ¿£Á©¸¸ ÁõÈıº Angelman syndrome
Q935 ijÃë22ÁõÈıº CATCH22 syndrome
Q936 ÀüÁ߱⿡¸¸ º¸ÀÌ´Â °á¼Õ Deletions seen only at prometaphase
Q937 ±âŸ º¹ÇÕ Àç¹è¿­À» µ¿¹ÝÇÑ °á¼Õ Deletions with other complex rearrangements
Q938 ±âŸ º¸Åë¿°»öüÀÇ °á¼Õ Other deletions from the autosomes
Q939 »ó¼¼ºÒ¸íÀÇ º¸Åë¿°»öüÀÇ °á¼Õ Deletions from autosomes, unspecified
Q95 ´Þ¸® ºÐ·ùµÇÁö ¾ÊÀº ±ÕÇü Àç¹è¿­ ¹× ±¸Á¶Ç¥ÁöÀÚ Balanced rearrangements and structural markers, NEC
Q95 ·Î¹öÆ®½¼ ¹× ±ÕÇüÀüÀ§ ¹× »ðÀÔ Robertsonian and balanced reciprocal translocations and insertions
Q950 Á¤»ó°³Ã¼¿¡¼­ÀÇ ±ÕÇü ÀüÀ§ ¹× »ðÀÔ Balanced translocation and insertion in normal individual
Q951 Á¤»ó°³Ã¼¿¡¼­ÀÇ ¿°»öü¿ªÀ§ Chromosome inversion in normal individual
Q952 ÀÌ»ó°³Ã¼¿¡¼­ÀÇ ±ÕÇüµÈ º¸Åë¿°»öü Àç¹è¿­ Balanced autosomal rearrangement in abnormal individual
Q953 ÀÌ»ó°³Ã¼¿¡¼­ÀÇ ±ÕÇüµÈ ¼º/º¸Åë¿°»öü Àç¹è¿­ Balanced sex/autosomal rearrangement in abnormal individual
Q954 Ç¥ÁöÀÚÀÌÁú¿°»öÁúÀ» °¡Áø °³Ã¼ Individual with marker heterochromatin
Q955 º¸Åë¿°»öü Ãë¾àºÎºÐÀ» °¡Áø °³Ã¼ Individual with autosomal fragile site
Q958 ±âŸ ±ÕÇüÀç¹è¿­ ¹× ±¸Á¶Ç¥ÁöÀÚ Other balanced rearrangements and structural markers
Q959 »ó¼¼ºÒ¸íÀÇ ±ÕÇüÀç¹è¿­ ¹× ±¸Á¶Ç¥ÁöÀÚ Balanced rearrangements and structural marker, unspecified
Q96 ÅÍ³Ê ÁõÈıº Turner's syndrome
Q960 ÇÙÇü 45, X Karyotype 45, X
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