高雄醫學大學圖書館 |

Language: English

Back

ISCN :an international system for hu...

International Standing Committee on Human Cytogenomic Nomenclature.

ISCN :an international system for human cytogenomic nomenclature (2016) /

Record Type:	Language materials, printed : Monograph/item
Title/Author:	ISCN :/ editors, Jean McGowan-Jordan, Annet Simons, Michael Schmid.
Reminder of title:	an international system for human cytogenomic nomenclature (2016) /
remainder title:	International system for human cytogenomic nomenclature (2016)
other author:	Schmid, M.
Corporate Body:	International Standing Committee on Human Cytogenomic Nomenclature.
Published:	Basel ;Karger, : c2016.,
Description:	vi, 139 p. :ill. ; : 28 cm.;
Notes:	"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."
Subject:	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