Mutation characterisation and microsatellite haplotype analysis of the CFTR gene

Mutational analysis of the proto-oncogenes c-fms and c-kit

Baker, D.A.

January 1995

SIGLEAvailable from British Library Document Supply Centre-DSC:DXN013387 / BLDSC - British Library D...

Genetic Examination of Children Suffering from Cystic Fibrosis

Ediba Saračević
Amira Redžić

February 2005

CFTR protein (cystic fibrosis trans membrane conductance regulator) is expressed in multiple epithel...

CFTR Gene as Determined with High-Resolution Melting Analysis To the Editor:

Cystic Fibrosis (omim Is

September 2016

one of the most common auto-somal recessive disorders in Cau-casians. It is caused bymutations in th...

Analysis of genomic CFTR DNA

Férec, Claude
Le Maréchal, Cédric
Audrézet, Marie-Pierre
Farinha, Carlos M.
Amaral, Margarida D.
Gallati, Sabina
Sanz, Javier
Steiner, Bernhard
Mouchel, Nathalie
Harris, Ann
Schwarz, Martin J.

August 2004

AbstractThere are numerous methodologies available for the analysis of genomic CFTR DNA. We present ...

Fluorescent multiplex microsatellites used to define haplotypes associated with 75 CFTR mutations from the UK on 437 CF chromosomes

Hughes, David
Taylor, Joanne
Wallace, Andrew
Tassabehji, May
McMahon, R
Hill, Alison
Nevin, Norman
Graham, Colin

January 1996

The cystic fibrosis (CF) transmembrane conductance regulator (CFTR) gene contains three highly infor...

Analysis of DNase I hypersensitive sites in the CFTR gene

Nuthall, H.

January 1998

SIGLEAvailable from British Library Document Supply Centre-DSC:D203796 / BLDSC - British Library Doc...

Regulation of expression of the CFTR gene

Moulin, D.S.

January 1998

SIGLEAvailable from British Library Document Supply Centre-DSC:D203787 / BLDSC - British Library Doc...

Analysis of genom rie-

Martin J. Schwarzf

October 2015

spital nal In hemis etics, y of O ter Ch Journal of Cystic Fibrosis 3 (2There are numerous methodolo...

Haplotype block structure study of the CFTR gene. Most variants are associated with the M470 allele in several European populations

F. Pompei
B. M. Ciminelli
C. Ciccacci
M. Koudova
S. Giorgi
M. Cerny
M. Des Georges
M. Claustres
C. Ferec
M. Macek Jr
G. . Modiano
BOMBIERI, Cristina
BELPINATI, Francesca
BEGNINI, Angela
PIGNATTI, Pierfranco

January 2006

An average of about 1700 CFTR (cystic fibrosis transmembrane conductance regulator) alleles from nor...

Direct sequencing of the complete CFTR gene: the molecular characterisation of 99.5% of CF chromosomes in Wales

Cheadle, Jeremy Peter
Goodchild, Mary C.
Meredith, Alison L.

January 1993

We have performed an extensive mutation analysis on 184 CF families In Wales. in our previous study,...

Mutations and sequence variations detected in the cystic fibrosis transmembrane conductance regulator (CFTR) gene: A report from the cystic fibrosis genetic analysis consortium

Tsui, LC

January 1992

Cystic fibrosis is the most common autosomal disorder in the Caucasian population. Since the descrip...

Molecular genetic analysis of fragile X syndrome

Wang, Q

January 1995

SIGLEAvailable from British Library Document Supply Centre- DSC:DX189562 / BLDSC - British Library D...

Molecular analysis of mutations at the hprt locus in primary human fibroblast lines

Morris, T
In collaboration with MRC Radiobiology Unit, Didcot (United Kingdom)
Council for National Academic Awards, London (United Kingdom)

January 1992

SIGLEAvailable from British Library Document Supply Centre- DSC:DX171945 / BLDSC - British Library D...

Identification of the M1101K mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene and complete detection of cystic fibrosis mutations in the Hutterite population

Schwartz, RH
Tsui, LC
Morgan, K
Klinger, KW
Richards, B
Anacleto, AI
Paradis, AJ
Markiewicz, D
Fujiwara, TM
Zielenski, J

January 1993

The Hutterite population is a genetic isolate with an increased incidence of cystic fibrosis (CF). P...

A comprehensive CFTR mutation analysis of German cystic fibrosis patients

Jochen Reiss
Ute Ellermeyer
Frauke Rininsl
Pia Ballhausen
Ulrike Lenz
Silke Wagner
Manfred Schlosser

January 1993

Cystic fibrosis (CF) is one of the most frequent genetic diseases among Caucasian populations and ca...

Mutational analysis of the proto-oncogenes c-fms and c-kit

Baker, D.A.

January 1995

SIGLEAvailable from British Library Document Supply Centre-DSC:DXN013387 / BLDSC - British Library D...

Genetic Examination of Children Suffering from Cystic Fibrosis

Ediba Saračević
Amira Redžić

February 2005

CFTR protein (cystic fibrosis trans membrane conductance regulator) is expressed in multiple epithel...

CFTR Gene as Determined with High-Resolution Melting Analysis To the Editor:

Cystic Fibrosis (omim Is

September 2016

one of the most common auto-somal recessive disorders in Cau-casians. It is caused bymutations in th...

Analysis of genomic CFTR DNA

Férec, Claude
Le Maréchal, Cédric
Audrézet, Marie-Pierre
Farinha, Carlos M.
Amaral, Margarida D.
Gallati, Sabina
Sanz, Javier
Steiner, Bernhard
Mouchel, Nathalie
Harris, Ann
Schwarz, Martin J.

August 2004

AbstractThere are numerous methodologies available for the analysis of genomic CFTR DNA. We present ...

Fluorescent multiplex microsatellites used to define haplotypes associated with 75 CFTR mutations from the UK on 437 CF chromosomes

Hughes, David
Taylor, Joanne
Wallace, Andrew
Tassabehji, May
McMahon, R
Hill, Alison
Nevin, Norman
Graham, Colin

January 1996

The cystic fibrosis (CF) transmembrane conductance regulator (CFTR) gene contains three highly infor...

Analysis of DNase I hypersensitive sites in the CFTR gene

Nuthall, H.

January 1998

SIGLEAvailable from British Library Document Supply Centre-DSC:D203796 / BLDSC - British Library Doc...

Regulation of expression of the CFTR gene

Moulin, D.S.

January 1998

SIGLEAvailable from British Library Document Supply Centre-DSC:D203787 / BLDSC - British Library Doc...

Analysis of genom rie-

Martin J. Schwarzf

October 2015

spital nal In hemis etics, y of O ter Ch Journal of Cystic Fibrosis 3 (2There are numerous methodolo...

Haplotype block structure study of the CFTR gene. Most variants are associated with the M470 allele in several European populations

F. Pompei
B. M. Ciminelli
C. Ciccacci
M. Koudova
S. Giorgi
M. Cerny
M. Des Georges
M. Claustres
C. Ferec
M. Macek Jr
G. . Modiano
BOMBIERI, Cristina
BELPINATI, Francesca
BEGNINI, Angela
PIGNATTI, Pierfranco

January 2006

An average of about 1700 CFTR (cystic fibrosis transmembrane conductance regulator) alleles from nor...

Direct sequencing of the complete CFTR gene: the molecular characterisation of 99.5% of CF chromosomes in Wales

Cheadle, Jeremy Peter
Goodchild, Mary C.
Meredith, Alison L.

January 1993

We have performed an extensive mutation analysis on 184 CF families In Wales. in our previous study,...

Mutations and sequence variations detected in the cystic fibrosis transmembrane conductance regulator (CFTR) gene: A report from the cystic fibrosis genetic analysis consortium

Tsui, LC

January 1992

Cystic fibrosis is the most common autosomal disorder in the Caucasian population. Since the descrip...

Molecular genetic analysis of fragile X syndrome

Wang, Q

January 1995

SIGLEAvailable from British Library Document Supply Centre- DSC:DX189562 / BLDSC - British Library D...

Molecular analysis of mutations at the hprt locus in primary human fibroblast lines

Morris, T
In collaboration with MRC Radiobiology Unit, Didcot (United Kingdom)
Council for National Academic Awards, London (United Kingdom)

January 1992

SIGLEAvailable from British Library Document Supply Centre- DSC:DX171945 / BLDSC - British Library D...

Identification of the M1101K mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene and complete detection of cystic fibrosis mutations in the Hutterite population

Schwartz, RH
Tsui, LC
Morgan, K
Klinger, KW
Richards, B
Anacleto, AI
Paradis, AJ
Markiewicz, D
Fujiwara, TM
Zielenski, J

January 1993

The Hutterite population is a genetic isolate with an increased incidence of cystic fibrosis (CF). P...

A comprehensive CFTR mutation analysis of German cystic fibrosis patients

Jochen Reiss
Ute Ellermeyer
Frauke Rininsl
Pia Ballhausen
Ulrike Lenz
Silke Wagner
Manfred Schlosser

January 1993

Cystic fibrosis (CF) is one of the most frequent genetic diseases among Caucasian populations and ca...

Mutational analysis of the proto-oncogenes c-fms and c-kit

Baker, D.A.

January 1995

SIGLEAvailable from British Library Document Supply Centre-DSC:DXN013387 / BLDSC - British Library D...

Genetic Examination of Children Suffering from Cystic Fibrosis

Ediba Saračević
Amira Redžić

February 2005

CFTR protein (cystic fibrosis trans membrane conductance regulator) is expressed in multiple epithel...

CFTR Gene as Determined with High-Resolution Melting Analysis To the Editor:

Cystic Fibrosis (omim Is

September 2016

one of the most common auto-somal recessive disorders in Cau-casians. It is caused bymutations in th...

Mutation characterisation and microsatellite haplotype analysis of the CFTR gene

Abstract

Extracted data

Mutation characterisation and microsatellite haplotype analysis of the CFTR gene

Abstract

Extracted data

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