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contradict Chromosome Antibody determination | chromosome breakage syndrome |
Danhuo Heterosome Principle | Chromosome Siduanbi deletion |
Chromosome Wuduanbi deletion | Chromosome outside code gene |
Jiashuang Kinetochore chromosome | Decimate Amniotic fluid check chromosome |
ring chromosome syndrome | Soma chromosome synapsis |
karyogram | Jinzhong Kinetochore chromosome |
Shuangjia Chromosome segregate | Non- Chromosome factor |
chromosome | chromosome |
chromosome karyotype | bacteriophage human artificial chromosome |
cytotaxonomy | chromosome |
nonchromosomal | autosomal dominant polycystic kidney |
People Chromosomoid Danbeixingleiqun | Breakdown Enter Accrete Enter Chromosome bridge circulation |
mark Chromosome Sector deletion syndrome | chromosome Three-body syndrome |
environmental pollution and chromosomal aberration | chromosome |
Chromosome Xianwei Concision Yuwei clone | vegetation Idioplasm exploit genome analysis |
saccharomycete Synthesise chromosome | chromosome Three-body syndrome |
crisp Heterosome locus Examine law | Autosome recessive a family disease |
Chromosome destabilization syndrome | chromosome |
mark chromosome | chromosome |
chromosome syndrome | autosomal dominant a family disease |
Breakage and reunion chromosome bridge circulation | mark Chromosome Sector deletion syndrome |
People Chromosomoid Danbeixingleiqun | Often Chromosome abnormalty a family disease |
chromosome | Chromosome Other part deletion |
other Autosomal deletion | other Designated chromosome abnormalty |
Chromosome just Come prometaphase deletion | character Chromosome abnormalty distaff phenotype |
normal Individual center chromosome inversion | Xuegao Decern Chromosome examine |
Conception Merger chromosome abnormalty | Decimate Floss check Child chromosome abnormalty |
Culture cell of Chromosome analyze | Lymph Kangguo (in biology) salivary gland chromosome antibody |
Amniotic fluid corpuscle chromosome examine | mark Chromosome Duanbi Deletion syndrome |
Distaff Together with Above and beyond Sange chromosomal | Danbei diploid chromosome gender determination |
Chromosome Emarginated to lose Gene diagnostic reagent | Import Multifunction chromosome Analyze Software |
oneness Chromosome gene library | Youyibei Chromosome of Being |
acrocentric chromosome acrolein | Chromosome agency gene transfer |
finger Chromosome map Borne Certain subparagraph | finger chromosomal aberration underlie |
Danbei diploid chromosome sex determination | blood Cousin chromosome commutator Trial |
Periphery blood corpuscle Chromosome examine | Amniotic fluid corpuscle Chromosome medium |
finger Chromosome map of Certain subparagraph | Accompany Host Genome Episode of |
character Chromosome abnormalty male phenotype | Fanzhuan Compounding circularity chromosome |
water Fish Distant hybirdization Species Chromosome map chart | mark Chromosome Changbi Sector element syndrome |
Autosome concealed sex inheritance model Hyphidrosis character Ectoblast Dysphasia syndrome | Dihao Chromosome Changbi Deletion syndrome |
Vegetation corpuscle And Chromosome engineering country priority facility | Often Chromosome apparent sex inheritance night frontal lobe epilepsy |
wean Autosome recessive Cerebella character dystaxia | vegetation Idioplasm exploit chromosome karyotyping |
vegetation Idioplasm exploit Chromosome band model analyze | Autosome concealed Sex inheritance von Willebrand disease |
Chromosome abnormalty model Dysgenesis Infertility | Autosome concealed Sex inheritance nature polycystic kidney |
mark Chromosome Changbi Sector element syndrome | Jiehao Chromosome Changbi Deletion syndrome |
Abnormal Individual Zhongping weighing Heterosome Huochang chromosomal rearrangement | Abnormal Individual Zhongping Hengchang chromosomal rearrangement |
pregnant Puerpera Prenatal bolting Examinatorial Chromosome and Code abnormal | Congenital malformation Buckle and Chromosome abnormalty personal history |
for the sake of Child Chromosome abnormalty Given pregnant Puerpera Medical treatment | Congenital malformation Buckle and Chromosome abnormalty of Singularise bolting examine |
Congenital testicle abort Male Together with Above and beyond couple chromosome | Other Sallet character Chromosome abnormalty male phenotype |
Other Sallet character Chromosome abnormalty distaff phenotype | Male together with Heterosome Congeneric embed connate |
Other sallet Autosomal Trisomy and Part trisomy | whole Chromosome trisomy Cytokinesis nondisjunction |
Chromosome just Come Prometaphase of repetition | Chromosome deletion Together with other Complexity and rearrangement |
whole Chromosome Element congeneric Chimera Karyokinesis nondisjunction | whole Chromosome monosomy Cytokinesis to keep someone at arm's length |
whole Chromosome trisomy Congeneric chimera karyokinesis nondisjunction | Article And Autosome relevant Metabolic disorder illness |
Together with Cortex next Infarct and Eukoencephalopathy Dedaqin Autosomal dominant arteriopathy | Congeneric chimera other Cell line together with Remarkable heterosome |
Congeneric inlay Soma Xiban Have alien quantitative chromosome | contradict Kinetochore contradict Autosome France production reductant |
Periphery blood Achroacyte chromosome medium | circularity Chromosome Huoshuang Kinetochore chromosome replace |
Karyotype together with Remarkable Heterosome exclusion connatural | Male Together with configuration Remarkable character chromosomal |
characterize Autosome crunchiness Part of Individual | Autosomal Trisomy and Part trisomy |
Autosome Regression nature Switzerland model Agammaglobulinemia | |