Related by context. All words. (Click for frequent words.) 65 dizygotic 64 monozygotic 64 dizygotic twins 64 monozygotic twins 61 monozygotic twin 61 HLA identical 60 autosomal recessive 59 Meckel Gruber 58 aneuploid 58 maternally inherited 58 homologous chromosomes 58 pluripotent embryonic 58 neuroligins 58 maternally transmitted 58 mutant alleles 58 fraternal twin pairs 58 orthologs 57 histocompatibility 57 R#W [002] 57 MLL2 57 nonhereditary 57 nonidentical twins 57 HLA matched 57 ENPP1 57 BARD1 56 autosomes 56 autosomal 56 hemolytic disease 56 IPAH 56 BMAL1 56 insertion deletion 56 germline mutations 56 mosaicism 56 twin transfusion 56 Li Fraumeni syndrome 56 sister chromatid 56 LPA gene 55 evolutionarily conserved 55 heterochromatic 55 mitochondrial DNA mtDNA 55 chromosomal deletions 55 fertilized egg splits 55 MLH1 55 Rh incompatibility 55 paternally inherited 55 cisplatin resistant 55 c KIT 55 dominantly inherited 55 chordate 55 genes predisposing 55 MYBPC3 55 hyper IgE syndrome 55 IKZF1 55 prion gene 55 fraternal triplets 55 de novo mutations 55 TACI mutations 55 microdeletion 55 uniparental 55 MLL gene 55 von Hippel Lindau 55 KRAS oncogene 55 HLA DRB1 55 beta globin 55 syngeneic 55 familial aggregation 54 D. melanogaster 54 Germline 54 gene rearrangements 54 Rh factor 54 spontaneous mutation 54 inherited maternally 54 germline cells 54 epigenetically 54 tricuspid atresia 54 fruitfly Drosophila 54 CDH1 54 transiently transfected 54 Leydig cells 54 IVF ICSI 54 familial clustering 54 holoprosencephaly 54 extramedullary 54 recessive trait 54 HLA typing 54 bilaterians 54 CpG DNA 54 progranulin gene 54 ligand receptor 54 p# mutation 54 TCF#L# gene 54 hamartomas 54 inbred strains 54 X. laevis 54 PON1 54 recessive genetic 54 transfusion syndrome 54 histone H4 54 underlying pathophysiology 54 inherited mutations 54 metaplasia 53 hematopoietic cell 53 genetic makeups 53 orthologous 53 nucleotide sequence 53 singleton pregnancy 53 phylogenetically 53 bone marrow mesenchymal stem 53 immunologically matched 53 differential gene expression 53 uterus didelphys 53 karyotype 53 vertebrate embryos 53 BRIP1 53 frameshift mutation 53 Apert syndrome 53 fertilized egg fails 53 genetic loci 53 meiotic 53 NPM1 gene 53 PTPN# 53 Epstein Barr Virus EBV 53 MYH9 gene 53 APOL1 53 cohesin 53 CC genotype 53 CFTR gene 53 exomes 53 #S rDNA 53 VNTR 53 prokaryote 53 ABO blood 53 PGD PGS 53 coexpression 53 novelty Schut 53 C#Y 53 haplogroups 53 MECP2 gene 53 maternally derived 53 sister chromatids 53 IgA deficiency 53 HHV 6 53 N. gonorrhoeae 53 T. vaginalis 53 autosomal dominant 53 MSH2 53 microchimerism 53 HAR1 53 allogenic 53 imprinted genes 53 chaperone proteins 53 indels 53 HbF 53 #q#.# [002] 53 DNA methylation patterns 53 microcephalin 53 lamivudine resistant 53 multigenic 53 Fragile X gene 53 #S rRNA 52 desmosomes 52 Sertoli cells 52 Y chromosomal 52 SCN5A 52 apoptosis pathway 52 BRCA1 BRCA2 52 missense mutations 52 gene duplications 52 Verlinsky 52 paralogs 52 allelic variants 52 RhD negative 52 heterozygous 52 Kabuki syndrome 52 LRP5 52 granulocyte 52 constitutively active 52 SMN1 52 monogenic 52 rhesus 52 RNA polymerases 52 vitro maturation 52 Fraternal twins 52 plexiform 52 preeclamptic 52 genetic lineages 52 BRAF V#E mutation 52 penetrance 52 fibroma 52 ABCB1 52 amino acid sequences 52 Vidaza ® 52 aneuploid cells 52 distantly related species 52 PALB2 52 HFE gene 52 sexually dimorphic 52 X. tropicalis 52 karyotypes 52 proband 52 intracellular signal transduction 52 homozygotes 52 chromosome rearrangements 52 M. pneumoniae 52 cytochrome b 52 endocasts 52 human leukocyte antigens 52 congenital disorders 52 genomic imprinting 52 virulence genes 52 pre eclamptic 52 C#T [002] 52 hypermethylated 52 pulmonary atresia 52 HLA markers 52 dyadic 52 proline rich 52 tumorigenicity 52 ADRB2 52 fig. S4 52 AVPR1A 52 operons 52 methyltransferase 52 Mycoplasma species 52 Yamanaka recipe 52 hydrops 52 homozygosity 52 NF1 gene 52 UGT#B# 52 MC1R gene 52 vasopressin receptor 52 eukaryotic cell 52 CagA 52 recessive mutation 52 congenital toxoplasmosis 52 totipotent 52 human leukocyte antigen 52 succinate dehydrogenase 52 genomic rearrangement 52 tyrosine phosphorylation 52 heterozygotes 52 clade B 52 activating mutation 52 GSTP1 52 nucleolar 52 TSC1 52 intergenic regions 52 excitation contraction 52 embryonic tissues 52 ependymomas 52 apolipoprotein E4 52 gene locus 52 Rb gene 52 #q# deletion syndrome 52 constitutively expressed 52 somatic mutations 52 Tatiana kidneys 51 aneuploidy 51 PCR RFLP 51 morphologic 51 Amino acid 51 hemagglutinin gene 51 breast cancer genes BRCA1 51 genotype phenotype 51 fig. S1 51 allele frequency 51 phthalate syndrome 51 UGT#A# * 51 NOTCH1 51 Pol IV 51 indel 51 autosomal dominant inheritance 51 recessive inheritance 51 klotho 51 neurofibromas 51 kinetochores 51 #q#.# deletion syndrome 51 primate genomes 51 figs. 51 tiny roundworm 51 methylenetetrahydrofolate reductase 51 CDK4 51 Gestational 51 homologous sequences 51 Crouzon Syndrome 51 centromeric 51 LRRK2 gene 51 proviral DNA 51 K ras mutations 51 MHC dissimilar 51 neoplastic 51 heritable 51 neural crest 51 antigen presenting cell 51 dysgenesis 51 HLA DRB1 * 51 fetal chromosomal abnormalities 51 amniotic cavity 51 aCGH 51 TOP2A 51 triplet pregnancies 51 CD4 + CD8 + 51 sickle cell hemoglobin 51 IL#R 51 dinucleotide 51 antiparallel 51 fraternal twins 51 ribosomal protein 51 haplotypes 51 hepatoma 51 gene amplification 51 transgene expression 51 chromosomal rearrangements 51 craniopagus 51 aetiological 51 CHEK2 51 APOE genotype 51 ALK gene 51 clinico pathological 51 genetic imprinting 51 sCJD 51 mammary cells 51 polygenic 51 orthologous genes 51 myelomeningocele 51 recessive mutations 51 KCNQ1 51 photosystem II 51 vacuolar 51 reproductively isolated 51 processive 51 protein tyrosine phosphatase 51 nucleotide substitution 51 common bile duct 51 sporadic ALS 51 C. albicans 51 uterus fallopian tubes 51 placental mammals 51 serine threonine kinase 51 Hypoplastic Left Heart 51 GTPases 51 nongenetic 51 CHEK2 gene 51 Xenopus laevis 51 PFAPA 51 familial ALS 51 CDKN2A 51 aneuploidies 51 CHO K1 51 polyploid 51 causative genes 51 hydronephrosis 50 vesicular stomatitis virus 50 hippocampal function 50 glycosyltransferase 50 CYP#D# gene 50 allelic 50 identical twins 50 teratoma 50 chromatid 50 gamete 50 neuritic 50 Volvox 50 activating mutations 50 leiomyoma 50 K#N 50 situs inversus 50 missense mutation 50 ribosomal genes 50 severe congenital neutropenia 50 Phenotypic 50 near Opuwo Namibia 50 conceptus 50 K RAS 50 chromosome #q 50 methylation patterns 50 PCR amplified 50 Selembu shows 50 hamartoma 50 perinatally 50 patrilineal 50 evolutionary conserved 50 Cathepsin B 50 pyloric stenosis 50 ligand induced 50 autistic regression 50 5 hydroxymethylcytosine 50 previously uncharacterized 50 neonatal respiratory distress 50 triplet 50 mutant allele 50 dyads 50 HOX genes 50 chordates 50 ectopic expression 50 epigenetic modification 50 MHC genes 50 segmental duplications 50 immunoreactive 50 #S ribosomal RNA 50 transcriptional repressor 50 pool dies unwept 50 epistasis 50 FLT3 50 chromatids 50 beta actin 50 aneuploidy screening 50 autosomal dominant disorder 50 Protein Kinase C 50 body louse genome 50 glia cells 50 multivariable analysis 50 CpG island 50 thrombophilia 50 ABCB1 gene 50 esophageal atresia 50 nulliparous 50 mtDNA 50 ploidy 50 symbiont 50 chromosome #p# [002] 50 allogeneic transplant 50 protein encoded 50 Homozygous 50 placental malaria 50 #S rRNA gene 50 polyandrous 50 mitochondrial genome 50 differentially regulated 50 Conjoined twin dies 50 mitochondrial gene 50 ETV1 50 haplotyping 50 homologues 50 clinicopathologic 50 G6PD deficiency 50 posttranslational modification 50 CHD7 50 clonal expansion 50 Ectopia Cordis 50 ERBB2 50 clonally 50 Eukaryotes 50 somites 50 hypoplastic 50 FGFR3 50 Kate Sofia Vassilieva 50 etiologic 50 enucleated 50 atresia 50 IVF embryo 50 DRD2 gene 50 multigene 50 EGFR TKIs 50 host = document.location.host 50 meiotic recombination 50 chimp genomes 50 evolutionary divergence 50 somatic mutation 50 X chromosome inactivation 50 intracytoplasmic 50 mucinous 50 Agrobacterium tumefaciens 50 homolog 50 medulloblastoma tumors 50 cysteines 50 lamellar 50 inferential statistics 50 miRNA expression 50 replicon 50 IUGR 50 isoenzyme 50 Twin Transfusion Syndrome 50 #HT#A receptor 50 isogenic 50 unmethylated 50 VEGFR1 50 intronic 50 excitatory synapses 50 congenital abnormality 49 spastic diplegia 49 tumor suppressors cytokines 49 fetal microchimerism 49 HLA genes 49 pheochromocytomas tumors 49 Immunohistochemical analysis 49 PTEN mutations 49 Arabidopsis genome 49 sperm fertilizes 49 allelic variation 49 blastomeres 49 chromosomal anomaly 49 V#F mutation 49 HLA DR4 immune 49 CETP VV 49 genotypic 49 mammalian organisms 49 craniofacial anomalies 49 proapoptotic 49 piRNAs 49 colocalization 49 non coding RNA 49 clinicopathological 49 Sanjae 49 VCFS 49 haploid 49 recessive genetic disorders 49 cytosolic 49 tumor specific antigen 49 HLA loci 49 chromosomal defect 49 Mendelian 49 genomewide 49 chromosomal rearrangement 49 Genetic mutations 49 congenital abnormalities 49 phenotypic differences 49 multi celled organisms 49 Hox gene 49 mtDNA mutations 49 FASPS 49 rFSH 49 IL#B 49 HepG2 cells 49 identical triplet 49 polyhydramnios 49 Male infertility 49 RET PTC rearrangements 49 ovulatory cycles 49 Alu elements 49 homologs 49 VSV G 49 Becker muscular dystrophy 49 ribosomal DNA 49 spindle fibers 49 hepatectomy 49 anterior pituitary 49 deacetylation 49 Froguel 49 congenital anomalies 49 centromeres 49 PIK3CA 49 parous 49 donor gametes 49 outbred 49 phosphorylates 49 polyadenylation 49 Western blotting 49 ZNF# 49 Clusterin 49 infertility miscarriages 49 metazoan 49 Sertoli cell 49 transduced 49 chromosome abnormalities 49 siRNA knockdown 49 malignant pancreatic 49 schizotypal 49 sensu lato 49 short hairpin RNAs 49 DQB1 * 49 reconstructed Lakshmi 49 embryonal 49 luteal 49 COL#A# 49 mammalian brains 49 eIF2 49 genetically identical 49 glutamic acid decarboxylase 49 hnRNP 49 bronchopulmonary dysplasia 49 L. pneumophila 49 Nf2 49 intergenic 49 microRNA expression 49 Spina bifida 49 Neisseria gonorrhoeae 49 neurexins 49 Biliary atresia 49 Morquio syndrome 49 epigenetic changes 49 glycosylase 49 HER2 HER2 49 phosphorylate 49 SHANK3 49 Mycoplasma genitalium 49 H. habilis 49 chromosome deletion 49 Genetic predisposition 49 Heterozygous 49 M. genitalium 49 microscopic colitis 49 2' O methyl 49 evolutionary lineages 49 splice variants 49 agenesis 49 prairie vole 49 nonoverlapping 49 spontaneous miscarriages 49 uncharacterized 49 phenotypic variation 49 probands 49 placenta praevia 49 inactivating mutations 49 mediastinitis 49 interconversion 49 SRY gene 49 MC1R 49 Deadlinepix 49 SNP rs# [002] 49 chronicity 49 stilbene 49 homologies 49 APOE ε4 49 CYP #D# 49 HLAs 49 coevolution 49 cytopathic 49 molecular scissors 49 splice variant 49 mirror neuron 49 BRAC2 49 parthenogenetic 49 genes CYP#C# 49 SOD1 gene 49 A. thaliana 49 TMEM#B 49 multicellularity 49 HER2 overexpression 49 maternal serum 48 homologue 48 CFTR gene mutations 48 alternatively spliced 48 transferase 48 monophyletic 48 phylogenetic 48 spore formation 48 synthases 48 chlamydial 48 wildtype 48 viral nucleic acids 48 TIMP 1 48 mutational analysis 48 idiopathic PAH 48 Simian Immunodeficiency Virus 48 endosymbiosis 48 LRAT 48 germline stem cells 48 phylogenetic trees 48 maternal antibodies 48 Leroy Esh 48 IRF6 gene 48 PI3K AKT 48 skeletal dysplasia 48 condensin 48 MTHFR gene 48 deuterostomes 48 coarctation 48 phylogenetic analyzes 48 chimpanzee genomes 48 KRAS BRAF 48 intrapartum 48 heritable variation 48 BCR ABL1 48 spontaneously aborted 48 marital cohabitation 48 microdeletions 48 Wolf Hirschhorn 48 H#Y 48 multivariate Cox 48 vimentin 48 Activating mutations 48 conjoined Egyptian 48 homologous 48 dimeric 48 familial pancreatic cancer 48 homodimer 48 auditory neuropathy 48 #p# [003] 48 maturational 48 CHDs 48 Glut1 48 Beckwith Wiedemann syndrome 48 p# subunit 48 evolvability 48 SLC#A# [001] 48 consanguineous 48 cis regulatory 48 immunofluorescence staining 48 ELBW infants 48 polynucleotide 48 #p#.# [001] 48 cardiac fibroblasts 48 EGFP 48 mature oocytes 48 microsatellite instability 48 Alport syndrome 48 rDNA 48 gestations 48 PRNP 48 adipogenic 48 duplicated chromosomes 48 oncogene addiction 48 gene inactivation 48 Hsp# [001] 48 X inactivation 48 genetic aberrations 48 glutamate glutamine 48 stem cell engraftment 48 chromosomally normal 48 K#R [002] 48 axon guidance 48 FADS2 gene 48 Fig. 2b 48 allele frequencies 48 intestinal microbiota 48 eukaryote 48 postnatally 48 chorioamnionitis 48 transfected 48 syndromic 48 genetic abnormality 48 HNPCC 48 abnormal p# 48 genetic relatedness 48 HG PIN 48 separated conjoined Guatemalan 48 Phylogenetic analysis 48 TMPRSS2 ERG fusion 48 sequence homology 48 p# p# 48 Angelman syndrome 48 KIF6 gene 48 apolipoprotein E APOE 48 severe hyperbilirubinemia 48 thyroid carcinoma 48 inhibin 48 transgenic mice expressing 48 bivariate 48 elevated serum ALT 48 unmutated 48 causative mutations 48 proteomic analysis 48 neonate 48 guanine G 48 chromosome #q# [002] 48 valine 48 tetramers 48 hypothalamic pituitary gonadal HPG 48 renal transplants 48 obstetrical complications 48 fascin 48 Fig. 1D 48 cGPS ® 48 oscillatory 48 RFLP 48 epithelia 48 olfactory receptor 48 Board probes octuplet 48 JAK mutations 48 β1 48 color Doppler sonography 48 spontaneous mutations 48 Gestational diabetes occurs 48 Supplementary Table 48 ductal breast cancer 48 CMV seropositive 48 forkhead 48 trimers 48 Fas ligand 48 metalloprotease 48 glycosylated 48 clades 48 bioengineered mice 48 assortative mating 48 anesthesia neuroanatomy obstetrics 48 peri natal 48 chromosomal aberrations 48 ICSI cycles 48 testicular germ cell 48 sisters uncles aunts 48 liver grafts 48 chromatin immunoprecipitation ChIP 48 H#K#me# 48 pulmonary hypoplasia 48 Neanderthals sprang 48 hypervascular 48 cholestasis 48 Crouzon syndrome 48 morphologically 48 antibody antigen 48 RNA sequences 48 murine leukemia 48 mutant proteins 48 splice junctions 48 GNAQ 48 thymidine 48 ectodermal dysplasia 48 hyperplastic 48 #S rRNA genes 48 genetically identical twins 48 Joubert Syndrome 48 Apolipoprotein E 48 HLA antigens 48 Fanconi 48 spheroidal 48 generalized vitiligo 48 M#V 48 tetramer 48 uncles aunts nieces nephews 48 kinesin motor 48 D#N 48 chromosomal anomalies 48 Moyamoya disease 48 phosphorothioate 48 telomeres shorten 48 dsDNA 48 parthenogenic 47 Nf1 47 noncoding 47 multiply uncontrollably 47 missense 47 NNRTI resistance 47 alexithymia 47 Spina bifida occurs 47 polydactylism 47 colorectal carcinogenesis 47 DU# [002] 47 photosystems 47 nucleotide substitutions 47 heterozygosity 47 giant danio 47 replicase 47 persistent pulmonary hypertension 47 human mammary epithelial 47 umbilical hernias 47 perinatal asphyxia 47 donor acceptor 47 Neuregulin 1 47 metazoans 47 IVF pregnancies 47 RhD 47 Rh positive 47 siderophore 47 genetic variants associated 47 thymidine kinase 47 intramolecular 47 ORFs 47 placental function 47 Thorough cooking kills 47 ductal lobular 47 gene loci 47 VKORC1 47 HLA DQ 47 P. falciparum malaria 47 extra siblings Anzaldo 47 transplanted marrow 47 intra uterine 47 cytidine 47 Sindbis 47 Preterm infants 47 mutated BRCA 47 aunts nieces nephews 47 CNTNAP2 47 rs# [004] 47 c Myb 47 FABP 47 Microtubule 47 regulator CFTR gene 47 truncus arteriosus 47 kinase domain 47 mechanotransduction 47 bladder exstrophy 47 affective psychosis 47 included Complices al 47 Viral RNA 47 protein conformation 47 alpha subunit 47 BRCA1 mutations 47 endophenotypes 47 Klinefelter syndrome 47 mesenchymal cell 47 thyroglobulin 47 chromosome #q# [001] 47 abnormal chromosomes 47 Alport Syndrome 47 Chantelle Stedman 47 SLITRK1 47 cypin 47 conjoined twin separation 47 meganuclease 47 epidermal cells 47 coding exons 47 micronutrient supplementation 47 patent ductus arteriosus 47 Vangl2 47 fungal genomes 47 homozygote 47 spectrin 47 gonadal 47 site directed mutagenesis 47 KIAA# 47 amyloid cascade 47 extra centrosomes 47 monotremes 47 SNPs pronounced snips 47 cathepsin B 47 Lori Kaplan Multz 47 hierarchical clustering 47 0 & 47 subcellular localization 47 chloroplast genome 47 trinucleotide 47 AFLP 47 female gamete 47 RNA transcription 47 multicellular organisms 47 Poisson regression 47 adenylate cyclase 47 G quadruplex 47 transcriptome sequencing 47 MTHFR 47 TP# gene 47 observable characteristics 47 ovules 47 differentially expressed genes 47 zygotic 47 primitive neuroectodermal tumors 47 pyrimidine 47 diploid 47 pharmacodynamic biomarkers 47 gambiae 47 UTRs 47 antitrypsin 47 transplanted kidneys 47 multiorgan 47 ontogenetic 47 polycystic 47 Charge Writ 47 genetic syndromes 47 genomic variants 47 variant allele 47 antisense oligonucleotides 47 childhood disintegrative disorder 47 genetically encoded 47 selfing 47 segmental duplication 47 vanA gene 47 ortholog 47 substrate specificity 47 egg follicles 47 embryo biopsy 47 mammary gland tumors 47 alpha catenin 47 Genotypic 47 mRNA transcripts 47 antireflux 47 gestational surrogates 47 perinatal morbidity 47 facial clefts 47 bisulfite sequencing 47 chromosomal defects 47 diffusion tensor 47 preterm deliveries 47 Haptoglobin 47 methicillin susceptible Staphylococcus aureus 47 fruitflies 47 microRNA molecule 47 immunological synapse 47 Haplogroup 47 cellular organelles 47 Hirschsprung disease 47 Blood transfusion 47 CRISPR 47 intersexuality 47 serostatus 47 PER2 47 amino acid residue 47 ataxias 47 phenotype 47 highly heritable 47 Secretase 47 Arp2 3 47 microarray gene expression 47 carboxyl terminal 47 neurocognitive dysfunction 47 Comparative Genomic Hybridization 47 Schematic representation 47 chromosomal disorders 47 developmental abnormalities 47 intracytoplasmic sperm injection ICSI 47 Anencephaly 47 phenotypes 47 Quantum mechanics 47 SLC#A# [002] 47 S. sanguinis 47 internalizing disorders 47 dialed Ybarra 47 adverse perinatal