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Search Results for 'Natlacad Genet'

Natlacad Genet published presentations and documents on DocSlides.

AmJHumGenet62105210611998GenotypePhenotypeCorrelationinAutosom

AmJHumGenet62105210611998GenotypePhenotypeCorrelationinAutosom

  • eloise
  • 10 Slides

Henniesetal.:Genotype/PhenotypeCorrelationinLIbond...

Diagnosis and management of Cornelia de Lange

Diagnosis and management of Cornelia de Lange

  • julia
  • 65 Slides

1 Syndrome: first international consensus statemen...

AmJHumGenet739579662003

AmJHumGenet739579662003

  • reagan
  • 10 Slides

MutationsinCapillaryMorphogenesisGene-2Resultinthe...

EpisodicNeurologicalChannelopathiesDevonPRyanandLouisJPtaNeuroscienc

EpisodicNeurologicalChannelopathiesDevonPRyanandLouisJPtaNeuroscienc

  • blanko
  • 11 Slides

,October21,20102010ElsevierInc. brought to you by ...

Sri Ramachandra Journal of Medicine June 2009 Vol II Issue 221Br

Sri Ramachandra Journal of Medicine June 2009 Vol II Issue 221Br

  • grace3
  • 4 Slides

R. Selvi a , Govind Raghav Saranya a , Jyotsna Mur...

Syndrome Review 1 Common

Syndrome Review 1 Common

  • obrien
  • 48 Slides

Trisomies and Sex Chromosome Variations Cynthia M...

COL4A1andCOL4A2mutationsanddiseaseinsightsintopathogenicmechanismsand

COL4A1andCOL4A2mutationsanddiseaseinsightsintopathogenicmechanismsand

  • emery
  • 14 Slides

 acids,withprolineoftenoccupyingtheYposition.Unli...

Current Biology Vol 19 No 5

Current Biology Vol 19 No 5

  • samantha
  • 2 Slides

of 6168 Dutch Europeans from the Rotterdam Study [...

Case Report

Case Report

  • caroline
  • 2 Slides

ISSN (O):2395 - 2822; ISSN (P):2395 - 2814 Annals ...

BibliographyBouwes Bavinck JNWeaver DDSubclavian artery supply disr

BibliographyBouwes Bavinck JNWeaver DDSubclavian artery supply disr

  • desha
  • 3 Slides

Klippel-Feil Anomaly Fig.51.4.Patient 5,adult.Spre...

Turner syndrome TS is a genetic disorder that was first described by

Turner syndrome TS is a genetic disorder that was first described by

  • esther
  • 5 Slides

171 Turner syndrome (TS) is a genetic disorder whi...

AmJHumGenet627927991998NovelMutationsintheConnexin26GeneGJB2T

AmJHumGenet627927991998NovelMutationsintheConnexin26GeneGJB2T

  • ethlyn
  • 8 Slides

Kelleyetal.:MutationsintheCx26Gene(GJB2)sensoryepi...

The impact of consanguinity on the Indian population Bittles AH Indi

The impact of consanguinity on the Indian population Bittles AH Indi

  • audrey
  • 8 Slides

Login Users online: 65 REVIEW ARTICLEYear : 2002 ...

a CNV its effect could only be manifested in a state of a single alle

a CNV its effect could only be manifested in a state of a single alle

  • paisley
  • 8 Slides

II-1II-2II-3II-4 ab OMIM Morbid Map ). We predict ...

MolecularMechanismsandTreatmentOptionsofNephropathicCystinosisAmerJama

MolecularMechanismsandTreatmentOptionsofNephropathicCystinosisAmerJama

  • summer
  • 14 Slides

ManoeJ.JanssenNephropathiccystinosisisasevere,mono...

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...

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 ...

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...

MechanismsofAgeingandDevelopment1222001921944Unwindingthemolecularb

MechanismsofAgeingandDevelopment1222001921944Unwindingthemolecularb

  • ida
  • 24 Slides

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

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, ...

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 ...

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...

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...

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  ...

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