語系/ Language:
繁體中文
English
KMU OLIS
登入
回首頁
切換:
標籤
|
MARC模式
|
ISBD
ISCN :an international system for hu...
~
International Standing Committee on Human Cytogenomic Nomenclature.
ISCN :an international system for human cytogenomic nomenclature (2016) /
紀錄類型:
書目-語言資料,印刷品 : Monograph/item
正題名/作者:
ISCN :/ editors, Jean McGowan-Jordan, Annet Simons, Michael Schmid.
其他題名:
an international system for human cytogenomic nomenclature (2016) /
其他題名:
International system for human cytogenomic nomenclature (2016)
其他作者:
Schmid, M.
團體作者:
International Standing Committee on Human Cytogenomic Nomenclature.
出版者:
Basel ;Karger, : c2016.,
面頁冊數:
vi, 139 p. :ill. ; : 28 cm.;
附註:
"Recommendations of the International Standing Committee on Human Cytogenomic Nomenclature, including new sequence-based cytogenomic nomenclature developed in collaboration with the Human Genome Variation Society (HGVS) Sequence Variant Description Working Group."
標題:
Genomics. -
ISBN:
9783318058574 (pbk.) :
ISCN :an international system for human cytogenomic nomenclature (2016) /
International Standing Committee on Human Cytogenomic Nomenclature.
ISCN :
an international system for human cytogenomic nomenclature (2016) /International system for human cytogenomic nomenclature (2016)editors, Jean McGowan-Jordan, Annet Simons, Michael Schmid. - Basel ;Karger,c2016. - vi, 139 p. :ill. ;28 cm.
"Recommendations of the International Standing Committee on Human Cytogenomic Nomenclature, including new sequence-based cytogenomic nomenclature developed in collaboration with the Human Genome Variation Society (HGVS) Sequence Variant Description Working Group."
Includes bibliographical references and index.
Historical introduction -- Normal chromosomes -- Symbols and abbreviated terms -- Karyotype designation -- Uncertainty in chromosome or band designation -- Order of chromosome abnormalities in the karyotype -- Normal variable chromosome features -- Numerical chromosome abnormalities -- Structural chromosome rearrangements -- Chromosome breakage -- Neoplasia -- Meiotic chromosomes -- In situ hybridization -- Miicroarrays -- Region-speciifc assays -- Sequence-based assays.
ISBN: 9783318058574 (pbk.) :NT1518
LCCN: 2016011865Subjects--Topical Terms:
232799
Genomics.
Index Terms--Genre/Form:
395275
Terminology.
LC Class. No.: QH431 / .I58 2016
Dewey Class. No.: 572.8
National Library of Medicine Call No.: QU 15
ISCN :an international system for human cytogenomic nomenclature (2016) /
LDR
:01716cam a2200265 a 4500
001
324071
005
20200318164216.0
008
200320s2016 sz a b 001 0 eng
010
$a
2016011865
020
$a
9783318058574 (pbk.) :
$c
NT1518
020
$a
3318058572 (pbk.)
035
$a
(DNLM)101678834
035
$a
00380270
040
$a
KMU
$d
KMU
042
$a
pcc
050
0 0
$a
QH431
$b
.I58 2016
060
1 0
$a
QU 15
082
0 0
$a
572.8
$2
23
110
2
$a
International Standing Committee on Human Cytogenomic Nomenclature.
$3
448000
245
1 0
$a
ISCN :
$b
an international system for human cytogenomic nomenclature (2016) /
$c
editors, Jean McGowan-Jordan, Annet Simons, Michael Schmid.
246
1
$a
International system for human cytogenomic nomenclature (2016)
260
$a
Basel ;
$a
New York :
$b
Karger,
$c
c2016.
300
$a
vi, 139 p. :
$b
ill. ;
$c
28 cm.
500
$a
"Recommendations of the International Standing Committee on Human Cytogenomic Nomenclature, including new sequence-based cytogenomic nomenclature developed in collaboration with the Human Genome Variation Society (HGVS) Sequence Variant Description Working Group."
500
$a
Published in Cytogenetic and Genome Research under the title ISCN 2016: An International System for Human Cytogenomic Nomenclature (2016).
504
$a
Includes bibliographical references and index.
505
0
$a
Historical introduction -- Normal chromosomes -- Symbols and abbreviated terms -- Karyotype designation -- Uncertainty in chromosome or band designation -- Order of chromosome abnormalities in the karyotype -- Normal variable chromosome features -- Numerical chromosome abnormalities -- Structural chromosome rearrangements -- Chromosome breakage -- Neoplasia -- Meiotic chromosomes -- In situ hybridization -- Miicroarrays -- Region-speciifc assays -- Sequence-based assays.
650
1 2
$2
96060
$a
Genomics.
$3
232799
650
1 2
$2
96060
$a
Cytogenetics.
$3
221216
650
0
$a
Genomics
$x
Terminology.
$3
448005
650
0
$a
Cytogenetics
$x
Terminology.
$3
448004
655
2
$a
Terminology.
$2
fast
$3
395275
700
1
$a
Schmid, M.
$q
(Michael)
$3
448003
700
1
$a
Simons, Annet.
$3
448002
700
1
$a
McGowan-Jordan, Jean.
$3
448001
筆 0 讀者評論
全部
後棟2F教師指定參考書區 2F Course Reserves Area (Rear Building)
前棟2F專業圖書區(圖書館) 2F Medical Monographic Collections (Front Building)
館藏
2 筆 • 頁數 1 •
1
條碼號
典藏地名稱
館藏流通類別
資料類型
索書號
使用類型
卷號
借閱狀態
預約狀態
備註欄
附件
00380270
前棟2F專業圖書區(圖書館) 2F Medical Monographic Collections (Front Building)
一般圖書
一般圖書 (Book)
QU15 I61 2016
一般使用(Normal)
在架
0
SDG3
預約
00380271
後棟2F教師指定參考書區 2F Course Reserves Area (Rear Building)
不流通
一般圖書 (Book)
QU15 I61 2016 c.2
一般使用(Normal)
在架
0
SDG3
2 筆 • 頁數 1 •
1
評論
新增評論
分享你的心得,請勿在此評論區張貼涉及人身攻擊、情緒謾罵、或內容涉及非法的不當言論,館方有權利刪除任何違反評論規則之發言,情節嚴重者一律停權,以維護所有讀者的自由言論空間。
Export
取書館別
處理中
...
變更密碼
登入