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Med Genet published presentations and documents on DocSlides.

AmJHumGenet697047112001GermlineMutationsinCauseaSubsetofCasesof

AmJHumGenet697047112001GermlineMutationsinCauseaSubsetofCasesof

  • gagnon
  • 8 Slides

Table1ClinicalFeaturesPresentinProbandsandFamilies...

Genetica32320012001KluwerAcademicPublishersPrintedintheNetherland

Genetica32320012001KluwerAcademicPublishersPrintedintheNetherland

  • joanne
  • 21 Slides

rawsequencedataexistsforeitherspeciesinpublicdatab...

Lack of MEF2A Mutations in Coronary Artery Disease

Lack of MEF2A Mutations in Coronary Artery Disease

  • ani
  • 10 Slides

Li Weng°, Nihan Kavaslar^, Anna Ustaszewska°, He...

NewandNotableWatchingPopulationsMeltDown

NewandNotableWatchingPopulationsMeltDown

  • hadley
  • 2 Slides

SubmittedJune1,2016,andacceptedforpublicationJune2...

MolecularCellVol12723734September2003Copyright2003byCellPressN

MolecularCellVol12723734September2003Copyright2003byCellPressN

  • nicole
  • 12 Slides

MolecularCellcludingthepresenceofoneclassIHDACsubu...

AmJHumGenet768658762005

AmJHumGenet768658762005

  • kimberly
  • 12 Slides

MicroduplicationandTriplicationof22q11.2:AHighlyVa...

AIMS Genetics

AIMS Genetics

  • skylar
  • 11 Slides

3 ( 2 ): 146 - 156 . DOI: 10.3934/genet.2016.2.1 ...

AmJHumGenet63173217421998VocalCordandPharyngealWeaknesswithAuto

AmJHumGenet63173217421998VocalCordandPharyngealWeaknesswithAuto

  • emery
  • 11 Slides

Feitetal.:VCPDMGeneMappedto5q31byDNAPooling Figure...

MolecularCellVol5969979June2000Copyright2000byCellPressFemaleM

MolecularCellVol5969979June2000Copyright2000byCellPressFemaleM

  • eddey
  • 11 Slides

MolecularCellessentiallythesamephenotype,massiveli...

P1VENFXYJanuary2020011714AnnualReviewsAR11424

P1VENFXYJanuary2020011714AnnualReviewsAR11424

  • oneill
  • 33 Slides

Annu.Rev.Physiol.2001.63:607Ð30Copyright2001byAnn...

PLEASE TURN TO PAGE 365 FOR DISCUSSION

PLEASE TURN TO PAGE 365 FOR DISCUSSION

  • audrey
  • 3 Slides

HOTO QUIZ 360 CUTIS Dirk M. Elston, MD, Departm...

HoweveritappearsthatCLSY1onlyaffectsapartofPolIVdependentRdDManditi

HoweveritappearsthatCLSY1onlyaffectsapartofPolIVdependentRdDManditi

  • rosemary
  • 14 Slides

mutantinordertoexaminetheDNAmethylomemutantplants(...

MechanismsofAgeingandDevelopment1222001921944Unwindingthemolecularb

MechanismsofAgeingandDevelopment1222001921944Unwindingthemolecularb

  • ida
  • 24 Slides

WS,Wernersyndrome;RPA,ReplicationproteinA;PCNA,Pro...

RareGeneticDiseasesNaturesExperimentsonHumanDevelopmentChelseaELee

RareGeneticDiseasesNaturesExperimentsonHumanDevelopmentChelseaELee

  • eloise
  • 15 Slides

iScience DepartmentofCellBiology,EmoryUniversity,A...

AmJHumGenet645385461999LimbMammarySyndromeANewGeneticDisorderw

AmJHumGenet645385461999LimbMammarySyndromeANewGeneticDisorderw

  • catherine
  • 9 Slides

brought to you by CORE View metadata, citation an...

IOSR Journal of Dental and Medical Sciences IOSR

IOSR Journal of Dental and Medical Sciences IOSR

  • elise
  • 4 Slides

- JDMS) e - ISSN: 2279 - 0853, p - ISSN: 2279 - 0...

4Nardi ACFerreira UNetto NR JrMagna LARodini ESORichieriCosta A

4Nardi ACFerreira UNetto NR JrMagna LARodini ESORichieriCosta A

  • eleanor
  • 4 Slides

and urine analysis were normal. In the follow up, ...

GENETICSBASIC DEFECTS1InheritanceaFamilial cases 50iAutosomal d

GENETICSBASIC DEFECTS1InheritanceaFamilial cases 50iAutosomal d

  • sadie
  • 3 Slides

b.E c.Orofacial c lefts Ectrodactyly-Ectodermal Dy...

Genet Res Oamb 1971 16 pp 24125 24With 1 textfigurePrinted in

Genet Res Oamb 1971 16 pp 24125 24With 1 textfigurePrinted in

  • mackenzie
  • 10 Slides

KWWSVGRLRUJ6...

AmJHumGenet653083171999HumanEhlersDanlosSyndromeTypeVIICandBov

AmJHumGenet653083171999HumanEhlersDanlosSyndromeTypeVIICandBov

  • mia
  • 10 Slides

brought to you by CORE View metadata, citation an...

ELLISVAN CREVELD SYNDROME

ELLISVAN CREVELD SYNDROME

  • josephine
  • 4 Slides

Yaşar Cesur , Sevil Arı Yuca , Abdurahman Üner ...

Int J Adv Res 909

Int J Adv Res 909

  • alyssa
  • 6 Slides

ISSN: 2320 - 5407 ...

REPORTMutationsinParkinsonDiseaseCarlesVilarinChristianWiderOwenARos

REPORTMutationsinParkinsonDiseaseCarlesVilarinChristianWiderOwenARos

  • elyana
  • 6 Slides

TheAmericanJournalofHumanGenetics,162–167,Jul...

mapsgenestodifferentphylogeneticranksinternodesaccordingtotheiremerg

mapsgenestodifferentphylogeneticranksinternodesaccordingtotheiremerg

  • ethlyn
  • 11 Slides

Figure1.Phylogenyanddivergencetime(mil-lionyearsag...

CellVol84911921March221996Copyright1996byCellPressFibroblastGr

CellVol84911921March221996Copyright1996byCellPressFibroblastGr

  • faith
  • 11 Slides

liver(twotissuesinwhichFGFR-3mRNAisnormallyexpress...

system that connects cytoskeletonremodelling and FMRP functionIntrodu

system that connects cytoskeletonremodelling and FMRP functionIntrodu

  • sophia2
  • 17 Slides

., 1991) and mapping and characterisation of thege...

FragileXandXLinkedIntellectualDisabilityFourDecadesofDiscoveryHerber

FragileXandXLinkedIntellectualDisabilityFourDecadesofDiscoveryHerber

  • jovita
  • 12 Slides

TheAmericanJournalofHumanGenetics,579–590,Apr...

LeadingEdgeGenomicAnalysisintheAgeofHumanGenomeSequencingTuuliLappalai

LeadingEdgeGenomicAnalysisintheAgeofHumanGenomeSequencingTuuliLappalai

  • harmony
  • 15 Slides

,March21,20192019ElsevierInc. platform,andwetheref...

A687VEZH2isagainoffunctionmutationfoundinlymphomapatientsChristinaR

A687VEZH2isagainoffunctionmutationfoundinlymphomapatientsChristinaR

  • stella
  • 4 Slides

2012FederationofEuropeanBiochemicalSocieties.Publi...

Genet Res Camb 1981 37 pp 27628 27Printed in Great BritainGame

Genet Res Camb 1981 37 pp 27628 27Printed in Great BritainGame

  • queenie
  • 10 Slides

KWWSVGRLRUJ6...

BrennerS1974ThegeneticsofCaenorhabditiselegansGenetics711509

BrennerS1974ThegeneticsofCaenorhabditiselegansGenetics711509

  • lydia
  • 7 Slides

Essentialgenes 5 Johnsen,R.C.,andBaillie,D.L.(1988...

LeightonPASaamJRIngramRSStewartCLandTilghmanSM1995

LeightonPASaamJRIngramRSStewartCLandTilghmanSM1995

  • ximena
  • 9 Slides

Development(2014)141,1805-1813doi:10.1242/dev.1014...

American Journal of Immunology 10 1 1422 2014 ISSN 1553619X 20

American Journal of Immunology 10 1 1422 2014 ISSN 1553619X 20

  • brianna
  • 9 Slides

Bhopal, India Tel: +91-7898664419 14  ...

Mol Gen Genet 1987

Mol Gen Genet 1987

  • fiona
  • 7 Slides

207:99-105 O Springer-Verlag 1987 Transposon Tn...

x0000x0000Proc Assoc Advmt Anim Breed Genet 24 431434x00

x0000x0000Proc Assoc Advmt Anim Breed Genet 24 431434x00

  • yvonne
  • 4 Slides

��Contributed paper��4...

EthnicityandmutationsinGJB2connexin26andGJB6connexin30inamulticul

EthnicityandmutationsinGJB2connexin26andGJB6connexin30inamulticul

  • valerie
  • 10 Slides

KEYWORDSHearingloss;Cochlearimplant;Todeterminethe...

SpringerVerlag 1992

SpringerVerlag 1992

  • pamela
  • 7 Slides

(1992) 101:381 387 Focus The fragile X syndrome:...

VANCES EN ODONTOESTOMATOLOGA305

VANCES EN ODONTOESTOMATOLOGA305

  • winnie
  • 6 Slides

endu-Osler common tools. The hemorrhage was stopp...

OriginalArticleEfcacyofaBicistronicVectorforCorrectionofSandhoffDisea

OriginalArticleEfcacyofaBicistronicVectorforCorrectionofSandhoffDisea

  • isla
  • 11 Slides

Received29September2018;accepted23October2018;http...

GeneticsShedsNewLightonCongenitalHydrocephalusBiologyDennisLalandAarno

GeneticsShedsNewLightonCongenitalHydrocephalusBiologyDennisLalandAarno

  • iris
  • 2 Slides

,July25,20182018PublishedbyElsevierInc. forlesstha...

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