paternal lineage

Related by string. paternal lineages * Paternal : Riley paternal grandmother . paternal grandfather . Semenya paternal grandmother . paternal ancestors . paternal grandparents . Paternal grandparents . paternal affection / lineages . Lineage : Assassin Creed Lineage . Embraer Lineage . ancestral lineage . distinct lineages . lineages diverged . illustrious lineage . lineage genealogy * *

Related by context. All words. (Click for frequent words.) 66 paternal ancestry 65 maternal lineage 60 Mitochondrial DNA 60 mtDNA 58 paternal lineages 58 mitochondrial DNA 57 Rh factor 57 proband 57 Haplogroup 57 Y STR 57 Y chromosomal 55 genetic ancestry 54 BRCA mutation 53 deleterious mutation 53 autosomal 52 ancestry 52 Y chromosome 52 chromosomal disorders 52 fetal nucleic acids 52 paternal grandfathers 52 ancestor 52 chromosomal anomalies 52 mutant allele 52 lineage 52 maternally inherited 52 paternal ancestor 51 SRY gene 51 paternally inherited 51 Mitochondrial Eve 51 recessive trait 51 mitochondrial DNA mtDNA 51 genomewide 51 fetal aneuploidy 51 aY chromosome 50 APOE genotype 50 nonidentical twins 50 haplogroups 50 polydactylism 50 microsatellite markers 50 APOE e4 50 Genetic testing 50 DNA 50 thrombophilia 50 allele frequencies 49 spontaneous mutation 49 BRCA2 gene 49 microbiomes 49 IgA deficiency 49 monozygotic twins 49 monozygotic 49 APOE4 49 ancestral lineage 49 genetic lineages 49 HNPCC 49 patrilineal 49 maternal grandmothers 49 apolipoprotein E gene 49 admixed populations 49 dizygotic twins 49 breast cancer genes BRCA1 49 BRCA genes 49 Dna 49 spontaneous mutations 49 aneuploidies 49 paternal 49 hereditary hemochromatosis 49 Negroid 49 mitochondrial mutations 49 FADS2 49 familial aggregation 49 haplotype 48 BRCA mutations 48 BARD1 48 MYH9 gene 48 Y Chromosome 48 genetic 48 hereditary disorders 48 maternal serum 48 causative genes 48 Single Nucleotide Polymorphisms 48 deoxyribonucleic acid 48 HLA genes 48 serologic 48 STK# gene 48 phenotypic variation 48 chromosomal anomaly 48 ancestory 48 genes predisposing 48 missense mutations 48 gestational diabetes mellitus 48 ultra rapid metabolizer 48 sCJD 48 placental malaria 48 Rh positive 48 methylation markers 48 MHC genes 48 epigenetic changes 48 BRCA2 mutation 48 paternal grandmothers 48 mitochondrial DNA sequence 48 TP# mutation 48 gynecological examination 48 genetic markers 48 chromosomal aberrations 47 maternal 47 Prostate Specific Antigen 47 phenotypic expression 47 BRCA2 gene mutation 47 recessive mutations 47 TGFBR1 * 6A 47 hereditary 47 ZNF# 47 germline mutations 47 miRNA expression profiles 47 genealogically 47 dizygotic 47 thrifty gene 47 heredity 47 mutant alleles 47 slave Sally Hemings 47 Genetic variation 47 genetic syndromes 47 colonoscopy flexible sigmoidoscopy 47 elevated CRP 47 recessive inheritance 47 QuantiFERON 47 chordate 47 HLA DRB1 47 cardiac channelopathies 47 BRCA2 mutations 47 microdeletions 47 familial pancreatic cancer 47 anthropometric measurements 47 intestinal biopsy 47 Ashkenazi Jewish 47 telomere lengths 47 rhesus 47 BRCA2 gene mutations 47 allelic 47 #q# deletion 46 aneuploidy screening 46 mosaicism 46 lineal descendants 46 mitochondrial genome 46 serologically 46 species Australopithecus afarensis 46 Mantoux 46 subclinical atherosclerosis 46 ApoE gene 46 faulty BRCA1 gene 46 BRCA breast cancer 46 mtDNA sequences 46 chromosomal alterations 46 chromosomally normal 46 mtDNA sequence 46 preimplantation genetic 46 hominoids 46 differentially expressed genes 46 JAK2 mutation 46 PALB2 46 Cora Crippen 46 BRAC2 46 fetal chromosomal abnormalities 46 Homozygous 46 Klinefelter syndrome 46 mutation 46 cytologic 46 KRAS BRAF 46 Stuttering tends 46 chromosomal abnormalities 46 G6PD deficiency 46 Simian Immunodeficiency Virus 46 maternal ancestor 46 advanced neoplasia 46 APOE gene 46 lineal descent 46 prenatal 46 prenatally diagnosed 46 modifier genes 46 maternal lineages 46 testicular germ cell 46 BRCA2 46 APOE epsilon 4 46 CDH1 46 dopamine transporter gene 46 haemochromatosis 46 jawed vertebrates 46 BRCA1 mutations 46 phthalate metabolites 46 mutated BRCA 46 genes BRCA1 46 Apert syndrome 46 HLA DQ2 46 aneuploidy 46 MSH2 46 genomic imprinting 46 recessive genes 46 parous 46 Ashkenazi Jews 46 genotyped 46 DNA testing 46 congenital adrenal hyperplasia CAH 46 semen sample 46 genotypic 46 T. vaginalis 46 HLA DQ 46 precancer 46 simple cheek swab 46 ramidus 46 Mendelian 46 BRCA2 mutation carriers 46 Cytogenetic 46 BRCA gene 46 exome 46 gametophyte 46 SMGF database 46 phylogenetic analyzes 46 GSTM1 gene 46 CCR5 delta# 46 congenital disorders 46 chromosome abnormality 46 highly heritable 45 sputum smear microscopy 45 MC1R 45 microdeletion 45 Neandertal 45 HLA B# 45 nucleotide substitution 45 MYH9 45 parentage 45 heterozygote 45 HLA antigens 45 hydroxy vitamin D 45 Ashkenazi Jew 45 heritable 45 Apobec3 45 #S rRNA 45 matrilineal 45 filiation 45 APOC3 45 sporadic ALS 45 haplogroup 45 phylogenetically 45 fetal microchimerism 45 fetal fibronectin 45 M. pneumoniae 45 orthologs 45 inbred strains 45 BRCA1 mutation 45 de novo mutations 45 M. leprae 45 cDNA libraries 45 mutated BRCA1 45 embryo biopsy 45 consanguineous marriage 45 maternally 45 BRCA1 gene 45 MEF2A 45 microchimerism 45 VUR 45 Genotypic 45 R#W [002] 45 immunochemical 45 clades 45 MTHFR gene 45 colorectal neoplasia 45 perinatally 45 imprinted genes 45 APOE ε4 45 TCF#L# gene 45 Alleles 45 paratuberculosis 45 positional cloning 45 tuberculin skin test 45 MLH1 45 breast cancer gene mutation 45 methylated DNA 45 BRCA1 gene mutation 45 CNTNAP2 45 allostatic load 45 immunohistochemical 45 nuchal translucency 45 viral nucleic acids 45 genetically homogeneous 45 Predisposition 45 paternal discrepancy 45 Chromosomal 45 Inkayacu 45 mtDNA mutations 45 mutated K ras 45 blastomeres 45 maternally derived 45 royal bloodline 45 tissue biopsies 45 descendants 45 colonoscopy sigmoidoscopy 45 serological tests 45 piRNAs 45 consanguineous 45 primordial germ cells 45 causative mutation 45 girl Hagemen 45 MCAD deficiency 45 nondemented 45 TACI mutations 45 genetic loci 45 HYPP 45 PAP smear 45 homozygosity 45 urine dipstick 45 DNA methylation patterns 45 HG PIN 45 TOMM# 45 nongenetic 45 genetic predisposition 45 autistic traits 45 Neanderthal fossils 45 ApoE4 45 IKZF1 45 alleles 45 immunofluorescent 45 MLL2 45 Haplotype 45 grandparent aunt 45 genetic abnormality 45 BRCA gene mutation 45 monogenic diabetes 45 ancestries 45 nucleus Chinnery 45 mitochondrial Eve 45 telomere length 45 linkage disequilibrium 44 HHV 6 44 lactose tolerance 44 causal variants 44 maternal grandfathers 44 extramedullary 44 Hair follicle 44 genetic trait 44 Mende tribe 44 Serology 44 somatic mutations 44 UGT#B# 44 morphological traits 44 immunochemical fecal occult 44 mitochondrial genomes 44 telomere DNA 44 probands 44 inherited maternally 44 prognostic markers 44 Neanderthal genes 44 genetic locus 44 APOL1 44 breast cancer gene mutations 44 abnormal lipid 44 C#Y mutation 44 Arabidopsis genome 44 RhD 44 Oxford Ancestors 44 serological 44 Mendelian disorders 44 allelic variation 44 susceptibility gene 44 DNA deoxyribonucleic acid 44 CDKN2A 44 body fatness 44 SLC#A# gene [001] 44 chromosomal imbalance 44 VNTR 44 Nasopharyngeal 44 inherited predisposition 44 nucleotide substitutions 44 abnormal chromosomes 44 TMPRSS2 ERG fusion 44 ELISA assays 44 #p# [001] 44 lineal ascendant 44 Mariamene 44 p# mutation 44 #S rDNA 44 recessive genetic 44 ADRB2 44 enamel defects 44 diploid genome 44 hydroxyvitamin D levels 44 preimplantation 44 MECP2 gene 44 salivary proteins 44 Amniocentesis 44 genetic makeup 44 Venter genome 44 Amborella 44 sister stepbrother stepsister 44 microalbumin 44 intersexed 44 Aneuploidy 44 chromosomal disorder 44 Socioeconomic status 44 familial clustering 44 urine cytology 44 cervical cytology 44 Jefferson Hemings 44 abnormal Pap test 44 neurodevelopmental outcome 44 SNP rs# [001] 44 intersexuality 44 aetiological 44 quantitative trait loci 44 Chlamydia trachomatis 44 BRCA gene mutations 44 prion gene 44 Aboriginality 44 non coding RNA 44 grandparent 44 chromosomal regions 44 AVPR1A 44 genetic relatedness 44 ELISAs 44 evolutionary lineage 44 Rhesus 44 CYP#E# gene 44 NHANES III 44 SMGF 44 HLA gene 44 V Leiden 44 Telomere length 44 Denisovan 44 endogamy 44 heterozygosity 44 Surname 44 chromosomal instability 44 BRIP1 44 #q#.# deletion syndrome 44 diagnosed prenatally 44 FeNO 44 prenatal diagnosis 44 ORMDL3 43 facial clefts 43 gene duplications 43 CETP VV 43 nonhereditary 43 genetic traits 43 Hirschsprung 43 mulattoes 43 #q# [001] 43 biological predisposition 43 preeclamptic 43 folate deficiency 43 genetic variant 43 penetrance 43 S. cerevisiae 43 genetic mutations 43 Gestational 43 Fragile X gene 43 epigenetic modifications 43 serum biomarkers 43 paternal ancestors 43 phylogenetic analysis 43 congenital toxoplasmosis 43 morphological characteristics 43 Raptorex kriegsteini 43 RhD negative 43 PCR assay 43 KRAS mutation 43 vaginal fluids 43 Evidence Clears 43 miRNA expression 43 aneuploid 43 Comparative genomics 43 gamete donors 43 apoE4 43 PCR RFLP 43 heritable variation 43 serologic tests 43 genomic alterations 43 Deoxyribonucleic acid DNA 43 introgression 43 eusociality 43 metabolomic profiles 43 cryptorchidism 43 frameshift mutation 43 klotho 43 chromosome deletion 43 SLC#A# [001] 43 medulloblastomas 43 MC1R gene 43 STAT4 43 autistic regression 43 descendant 43 reassortants 43 DiGeorge syndrome 43 HLA markers 43 Y chromosomes 43 Leptospira 43 heel prick test 43 A. thaliana 43 male prairie voles 43 Gene Mutation 43 serum selenium 43 p# mutations 43 D Dimer 43 KCNQ1 43 Meckel Gruber 43 Fecal occult blood 43 microsatellite loci 43 serum ferritin 43 buccal swabs 43 sputum sample 43 cervical biopsies 43 mutational analysis 43 mitochondrial DNA mutations 43 germline cells 43 VKORC1 43 genetic recombination 43 socioeconomic status SES 43 hepatitis B infection 43 A. ramidus 43 phthalate exposure 43 methylation patterns 43 ABCB1 gene 43 Spinal muscular atrophy 43 Chlamydia pneumoniae 43 ancestors 43 serologic testing 43 abnormal lipid levels 43 ApoE4 gene 43 chromosomal 43 haplotypes 43 multigene 43 heterozygotes 43 pre eclamptic 43 mitochondrial proteins 43 epigenetic inheritance 43 varicocele 43 rectal swab 43 relatedness 43 polygenic 43 genetic abnormalities 43 Gram stain 43 airway responsiveness 43 aneuploid cells 43 germline 43 histocompatibility 43 prion infection 43 saliva sample 43 organochlorine compounds 43 KRAS mutations 43 familial ALS 43 body louse genome 43 KIAA# 43 human leukocyte antigen 43 microscopic colitis 43 splice junctions 43 adenomatous polyps 43 stool sample 43 CCL#L# 43 rectal palpation 43 heritable traits 43 enterotypes 43 cell lysate 43 herpesviruses 43 maternally transmitted 43 ELISpot 43 genetic polymorphisms 43 epigenetic regulation 43 HPV genotypes 43 finger prick blood 43 Apolipoprotein E 43 epistasis 43 HMGA2 gene 43 thyroid stimulating hormone 43 PON1 43 breast carcinomas 43 genetic makeups 43 chromosome abnormalities 43 PSA screening 43 fa'afafine 43 karyotype 43 prostate specific 43 obstructive coronary artery 43 Genotypes 43 phenotypic characteristics 43 Phenotypic 43 jus sanguinis 43 chromosomally 43 telomeres shorten 43 congenital hypothyroidism 43 vasa previa 43 facial attractiveness 43 Placental 43 meiotic recombination 43 subfertility 42 thyroid dysfunction 42 undiagnosed celiac disease 42 monophyletic 42 vitro maturation 42 CNVs 42 PCR amplification 42 offspring 42 assortative mating 42 NF1 gene 42 retrospective cohort 42 Serologic 42 specific antigen 42 elevated serum ALT 42 Li Fraumeni 42 Austria Gruner Veltliner 42 BRCA 42 nucleosome positioning 42 Surnames 42 endophenotypes 42 MCADD 42 Telomere 42 gene amplification 42 CAG repeats 42 Stephanie Belloc 42 stool specimen 42 HFE gene 42 EtG 42 Furthermore Rielle 42 FMR1 gene 42 lineages 42 greatgrandfather 42 HLA typing 42 QTLs 42 gene predisposing 42 allelic variants 42 Talpiot tomb 42 fFN 42 #q#.# [001] 42 C#Y 42 KIBRA 42 corona virus 42 chorionic villi 42 FGFR2 gene 42 isotopic analysis 42 HPV 42 CHEK2 42 genome rearrangements 42 neuroligins 42 proteomic analysis 42 Reynolds Risk Score 42 Leydig cells 42 Ashkenazic Jews 42 evolvability 42 transferrin saturation 42 Toxoplasma 42 HLA molecules 42 anogenital distance 42 coprolites 42 choline intake 42 haplotype map 42 MAOA gene 42 metaplasia 42 transcriptomes 42 methylation 42 taxon 42 BMI percentile 42 heritability 42 testicular tumors 42 semen saliva 42 Trichinella 42 masculine traits 42 histone modification 42 D. melanogaster 42 Genetic Variation 42 C#BL/#J 42 Li Fraumeni syndrome 42 Canis familiaris 42 Ankhesenamun 42 FTO variant 42 mature oocytes 42 DRD2 gene 42 inbreeding coefficient 42 IUGR 42 laforin 42 abnormal cytology 42 chlamydial infection 42 DHEAS 42 genetic susceptibility 42 HIV tropism 42 NPM1 gene 42 Identification Kit 42 CFTR gene mutations 42 rhesus negative 42 HLA identical 42 singleton pregnancies 42 multiple logistic regression 42 elevated homocysteine 42 abnormal mammogram 42 Neandertal DNA 42 BAC clones 42 ASCUS 42 HPV# 42 Stanford Binet 42 chloroplast genome 42 apoE 42 tandem mass spectrometry 42 progranulin gene 42 inherited genetic mutation 42 chromosomal defect 42 Haptoglobin 42 chromosomal deletions 42 genetical 42 serological testing 42 homologies 42 faecal occult blood 42 admixed 42 nucleotide sequence 42 genomic aberrations 42 multivitamin supplementation 42 genetically hardwired 42 chromosome translocations 42 globin 42 assortative 42 heritable diseases 42 behavioral disinhibition 42 lactase persistence 42 sonographic diagnosis 42 Paternal 42 fecal occult blood 42 PTPN# 42 unexplained mental retardation 42 genes predispose 42 genetically 42 skin scrapings 42 primate lineage 42 descendents 42 flexible sigmoidoscopy 42 urine specimens 42 genetic mutation 42 recurrent miscarriages 42 allele 42 chimp genomes 42 androgen receptor gene 42 microsatellite instability 42 polyploidy 42 genetic determinants 42 precancerous polyp 42 subgenus 42 PSA velocity 42 periodontal infection 42 human leukocyte antigens 42 hemochromatosis 42 TP# gene 42 pancreatic tissue 42 Single Nucleotide Polymorphisms SNPs 42 conserved sequences 42 BRCA1 42 defective gene 42 recessive gene 42 Human Leukocyte Antigen 42 single nucleotide polymorphism 42 chromatin proteins 42 Wolbachia strains 42 autoimmune thyroid 42 Child Behavior Checklist 42 genetic variants associated 42 chromosomal defects 42 incomplete penetrance 42 hereditary breast cancer 42 #p#.# [001] 42 FGFs 42 PCR amplified 42 breast cancer subtypes 42 SLC#A# [002] 42 Paternity tests 42 vertebrate embryos 42 thiopurine 42 mutated gene 42 mRNA transcripts 42 unborn fetus 42 recessive traits 42 ribosomal genes 42 pseudogenes 42 fetuin 42 genes 42 genomewide association study 42 Lafora disease 42 filicide 42 autosomes 42 rs# [002] 42 CIN2 + 42 IGF2 42 antigen PSA 42 perinatal outcomes 41 gene expression patterns 41 DNA Deoxyribonucleic Acid 41 autosomal recessive disease 41 G#S mutation 41 Stillbirths 41 LRRK2 gene 41 congenital CMV infection 41 genetic polymorphism 41 tube fertilization 41 Dawes Rolls 41 dna 41 diffuse gastric 41 genetic variability 41 differential gene expression 41 Bioassays 41 functional annotation 41 FMR1 41 PITX2 41 malarial parasites 41 polyploid 41 CRISPR Cas 41 major histocompatibility complex 41 invitro 41 susceptibility genes 41 Yamanaka recipe 41 vaginal swabs taken 41 S. neurona 41 marital statuses 41 cynomolgus macaques 41 HLA G 41 gene locus 41 digital rectal examination 41 TRF1 41 neoplasias 41 LRAT 41 CFTR gene 41 neurodevelopmental outcomes 41 gene mutation 41 breast cancer susceptibility genes 41 LQTS 41 #BP# 41 X chromosome 41 ovarian hormones 41 ancestral 41 sister chromatid 41 Dolphus Shields 41 nongenetic factors 41 totipotent 41 genetically predetermined 41 inhibin 41 hemolytic disease 41 FUS protein 41 differentially expressed proteins 41 bone density scans 41 EGFR mutation status 41 dietary intakes 41 HeLa cell 41 Treponema pallidum 41 Parentage 41 oropharyngeal cancer 41 Dr. Loeken 41 HbF 41 abnormal hemoglobin 41 prepubertal 41 homozygote 41 folate intake 41 Prostate Specific Antigen PSA 41 epigenetic modification 41 familial adenomatous polyposis 41 greatgrandmother 41 serology 41 Pubic lice 41 Incas Aztecs 41 autosomal recessive 41 Now Be Replicated 41 biochemical signaling pathway 41 semen specimen 41 prenatal testosterone 41 gene variant 41 neural tube defect 41 observable traits 41 USPSTF recommends 41 gene BRCA2 41 histone modifications 41 chi squared 41 radiocarbon 41 surrogacies 41 serum samples 41 testicular biopsy 41 FGFR2 41 mouth swabs 41 estrogen metabolites 41 amniocentesis 41 hormone hCG 41 fetal oxygen saturation 41 phenotype 41 inhibin B 41 Salmonella spp 41 Clusterin 41 pyloric stenosis 41 gut microbes 41 Brugada Syndrome 41 chromosome #p# [001] 41 Genetic 41 haplotyping 41 polydactyly 41 godparent 41 somatic mutation 41 endogenous retroviruses 41 coinfection 41 CGG repeats 41 malaria endemic regions 41 inheritable diseases 41 neural crest 41 #S rRNA gene 41 outcrossing 41 bivariate 41 chromosome #q#.# [002] 41 Australopithecus anamensis 41 GFP gene 41 serum protein biomarkers 41 Wwox 41 CYP#C# [002] 41 lincRNA 41 pelvic ultrasound 41 PTEN mutations 41 KLF4 41 sentinel node 41 gonadal 41 uncharacterized genes 41 chromosome #q# [001] 41 subclinical 41 genetics 41 coding exons 41 RFLP 41 forensic casework 41 RT qPCR 41 MSMB 41 atopy 41 polycystic ovarian syndrome PCOS 41 colon rectal 41 mutated genes 41 H2AX 41 MTHFR 41 Multiple logistic regression 41 folate concentrations 41 mammary stem cells 41 CYP#D# gene 41 Septin 9 41 antral follicles 41 Folic acid deficiency 41 flavivirus 41 susceptibility alleles 41 sexually reproducing 41 hypermethylated 41 follicle stimulating hormone FSH 41 SCN1A 41 chlamydia sexually transmitted 41 Australopithecus genus 41 sonographic evaluation 41 evolutionary origins 41 chordates 41 Paranthropus robustus 41 pesticide metabolites 41 adrenal function 41 PCA3 gene 41 NNRTI resistance 41 Massospondylus 41 epigenetic reprogramming 41 carotid bruit 41 microRNA expression 41 trisomy 41 homologs 41 cDNA microarray 41 tubule 41 Mental retardation 41 genomic sequence 41 periodontal pathogens 41 DICER1 gene 41 descendent 41 microcephalin 41 Klinefelter Syndrome 41 grandparental 41 Scientists Decode 41 number variations CNVs 41 selfing 41 miscarriages stillbirths 41 sociodemographic variables 41 urolithiasis 41 Genetic predisposition 41 promoter hypermethylation 41 ploidy 41 SCA5 41 exome sequencing 41 heterozygous 41 Sanger sequencing 41 Alcoholism COGA 41 Mycobacterium leprae 41 multigenic 41 ultraconserved 41 COMT gene 41 prostate biopsy 41 fetal malformations 41 bone density measurements 41 Eadgyth 41 mitochondrial gene 41 Prox1 41 PrPSc 41 lentiviruses 41 thyrotropin levels 41 homologous genes 41 urine saliva 41 TEP1

Back to home page