MARC record from Internet Archive

LEADER: 03903cam 2200733 a 4500
001 ocm37519678
003 OCoLC
005 20200519210614.0
008 970815s1997 nyua bci 001 0 eng
010 $a 97037684
040 $aDNLM/DLC$beng$cDLC$dNLM$dUKM$dBAKER$dBTCTA$dYDXCP$dZWZ$dGEBAY$dOCLCQ$dTVG$dBDX$dOCLCF$dOCLCQ$dOCLCO$dOCLCQ$dUWO$dOCLCO$dCNO$dOCLCO$dOCLCA
015 $aGB9775781$2bnb
016 7 $a9713326$2DNLM
019 $a38040442
020 $a0471243329$q(cloth ;$qalk. paper)
020 $a9780471243328$q(cloth ;$qalk. paper)
035 $a(OCoLC)37519678$z(OCoLC)38040442
037 $a24573$bTVG
050 00 $aQS677$bB732 1997
060 00 $aZQS 677$bB732c 1997
082 00 $a616/.042$221
100 1 $aBorgaonkar, Digamber S.
245 10 $aChromosomal variation in man :$ba catalog of chromosomal variants and anomalies /$cDigamber S. Borgaonkar.
250 $a8th ed.
260 $aNew York :$bWiley-Liss,$c℗♭1997.
300 $aciv, 1175 pages :$billustrations ;$c26 cm
336 $atext$btxt$2rdacontent
337 $aunmediated$bn$2rdamedia
338 $avolume$bnc$2rdacarrier
504 $aIncludes bibliographical references and indexes.
520 1 $a"Chromosomal Variation in Man: A Catalog of Chromosomal Variants and Anomalies, Eighth Edition provides an unparalleled means of reviewing the world literature on all common and rare chromosomal alterations and abnormalities. Organized for easy access, coverage is divided into the three main subject areas: variations and anomalies, numerical anomalies, and chromosomal breakage syndromes. The Catalog documents information on the availability of mutant cell lines and presents chromosome alterations with a list that cross-references band numbers." "This updated and expanded edition contains nearly 19,000 entries - 3,000 more than the previous edition - including new or expanded coverage of structural anomalies, new banding techniques, spectral karyotyping of chromosomes, FISH, UPD, and PRINS."--BOOK JACKET.
610 24 $aT♯łp Faku ltesi Ku tu phanesi.
650 0 $aHuman chromosome abnormalities$vCatalogs and collections.
650 0 $aHuman chromosomes$vCatalogs and collections.
650 7 $aAberrations chromosomiques.$2fmesh
650 7 $aAberrations chromosomiques, maladies.$2fmesh
650 7 $aHuman chromosome abnormalities.$2fast$0(OCoLC)fst00962907
650 7 $aHuman chromosomes.$2fast$0(OCoLC)fst00962918
650 7 $aChromosomenanomalie$2gnd
650 7 $aVerzeichnis$2gnd
650 7 $aChromosomenaberration$2gnd
650 07 $aChromosomenanomalie.$2swd
650 07 $aVerzeichnis.$2swd
650 07 $aChromosomenaberration.$2swd
650 12 $aChromosome Aberrations.$0https://id.nlm.nih.gov/mesh/D002869
655 7 $aCatalogs and collections.$2fast$0(OCoLC)fst01423697
655 2 $aIndex.$0https://id.nlm.nih.gov/mesh/D020481
776 08 $iOnline version:$aBorgaonkar, Digamber S.$tChromosomal variation in man.$b8th ed.$dNew York : Wiley-Liss, ℗♭1997$w(OCoLC)605388511
776 08 $iOnline version:$aBorgaonkar, Digamber S.$tChromosomal variation in man.$b8th ed.$dNew York : Wiley-Liss, ℗♭1997$w(OCoLC)607828287
856 41 $3Table of contents$uhttp://catdir.loc.gov/catdir/toc/wiley024/97037684.html
856 42 $3Publisher description$uhttp://catdir.loc.gov/catdir/description/wiley032/97037684.html
938 $aBaker & Taylor$bBKTY$c250.00$d254.95$i0471243329$n0003061843$sactive
938 $aBrodart$bBROD$n51524279$c$279.95
938 $aBaker and Taylor$bBTCP$n97037684
938 $aYBP Library Services$bYANK$n1414535
029 1 $aAU@$b000013397401
029 1 $aAU@$b000020154731
029 1 $aGEBAY$b2797909
029 1 $aHEBIS$b06130011X
029 1 $aNLM$b9713326
029 1 $aYDXCP$b1414535
029 1 $aZWZ$b032388993
994 $aZ0$bP4A
948 $hNO HOLDINGS IN P4A - 141 OTHER HOLDINGS