| Record ID | marc_loc_updates/v36.i02.records.utf8:14531140:1938 |
| Source | Library of Congress |
| Download Link | /show-records/marc_loc_updates/v36.i02.records.utf8:14531140:1938?format=raw |
LEADER: 01938nam a22003138a 4500
001 2008000023
003 DLC
005 20080110105218.0
008 080103s2008 nyu b 001 0 eng
035 $a(DNLM)101462700
010 $a 2008000023
020 $a9781604562460 (hardcover)
040 $aDNLM/DLC$cDLC
042 $apcc
050 00 $aQH430$b.G4565 2008
060 10 $aQZ 50$bG32494 2008
082 00 $a616/.042$222
245 00 $aGenetic inheritance patterns /$cRen Kimura (editor).
260 $aNew York :$bNova Science Publishers,$cc2008.
263 $a0805
300 $ap. ;$ccm.
504 $aIncludes bibliographical references and index.
505 0 $aShort communications myotonic dystrophy type 1 and 2 as a repeat disease / Hajime Arahata, Hirokazu Furuya -- Using 1-2 individual organisms to address population genetic questions / Jianping Xu -- Research and review studies Nijmegen breakage syndrome: a DNA double strand breaks repair defective disorder / Alessandra di Masi, Francesco Berardinelli, Antonio Antoccia -- Modelling genetic and physiological heterogeneity / Mogens Fenger -- Polymorphisms in CCR5 chemokine receptor gene / Emi E. Nakayama, Tatso Shioda -- Inheritance of litter size in mammals: different patterns in different populations / Tatiana I. Axenovich, Pavel M. Borodin -- Gaining a comprehensive understanding of the role of heritable, molecular genetic variation in mate choice and mating related genes / Lisa Horth -- Osteogenesis imperfecta / Alexander K.C. Leung, Danièle Pacaud, Jean François Lemay -- Recent findings in Danon disease, a rare x-linked dominant disorder with multisystem involvement / Marina Fanin, Anna Chiara Nascimbeni, Marco Spinazzi.
650 0 $aGenetics.
650 12 $aInheritance Patterns$xphysiology.
650 22 $aGene Expression.
650 22 $aGenetic Diseases, X-Linked.
650 22 $aVariation (Genetics)$xphysiology.
700 1 $aKimura, Ren,$d1958-