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Publications by A L Meredith

Bilateral Split Hand and Split Foot Malformation in a Boy With a De Novo Interstitial Deletion of 7q21.3

Journal of Medical Genetics

Genetics

1991

English

Application of a Closely Linked Polymorphism of Restriction Fragment Length to Counselling and Prenatal Testing in Families With Myotonic Dystrophy.

BMJ

1986

English

Related publications

Recurrent Streptococcus Pneumoniae Meningitis in a Child With Split Hand and Foot Malformation and Undiagnosed Mondini Dysplasia

Journal of Developmental and Physical Disabilities

Physical Therapy

Sports Therapy

Rehabilitation

Educational Psychology

Developmental

2015

English

Homozygous Sequence Variants in the WNT10B Gene Underlie Split Hand/Foot Malformation

Genetics and Molecular Biology

Genetics

Molecular Biology

2018

English

Absent Expression of the Osteoblast-Specific Maternally Imprinted Genes,DLX5andDLX6,causes Split Hand/Split Foot Malformation Type I

Journal of Medical Genetics

Genetics

2014

English

Rare Missense Variant p.Ala505Ser in the ZAK Protein Observed in a Patient With Split-Hand/Foot Malformation From a Non-Consanguineous Pedigree

Journal of International Medical Research

English

Split Hand/Split Foot Deformity and LADD Syndrome in a Family: Overlap Between the EEC and LADD Syndromes.

Journal of Medical Genetics

Genetics

1993

English

17p13.3 Genomic Rearrangement in a Chinese Family With Split-Hand/Foot Malformation With Long Bone Deficiency: Report of a Complicated Duplication With Marked Variation in Phenotype

Orphanet Journal of Rare Diseases

English

A Novel Heterozygous Intragenic Sequence Variant in DLX6 Probably Underlies First Case of Autosomal Dominant Split-Hand/Foot Malformation Type 1

Molecular Syndromology

Genetics

2016

English

Fine Mapping of the Split-Hand/Split-Foot Locus (SHFM3) at 10q24: Evidence for Anticipation and Segregation Distortion

American Journal of Human Genetics

Genetics

1999

English

Phenotypic and Genetic Characterization of a Patient With a De Novo Interstitial 14q24.1q24.3 Deletion

Molecular Cytogenetics

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by A L Meredith

Bilateral Split Hand and Split Foot Malformation in a Boy With a De Novo Interstitial Deletion of 7q21.3

Application of a Closely Linked Polymorphism of Restriction Fragment Length to Counselling and Prenatal Testing in Families With Myotonic Dystrophy.

Related publications

Recurrent Streptococcus Pneumoniae Meningitis in a Child With Split Hand and Foot Malformation and Undiagnosed Mondini Dysplasia

Homozygous Sequence Variants in the WNT10B Gene Underlie Split Hand/Foot Malformation

Absent Expression of the Osteoblast-Specific Maternally Imprinted Genes,DLX5andDLX6,causes Split Hand/Split Foot Malformation Type I

Rare Missense Variant p.Ala505Ser in the ZAK Protein Observed in a Patient With Split-Hand/Foot Malformation From a Non-Consanguineous Pedigree

Split Hand/Split Foot Deformity and LADD Syndrome in a Family: Overlap Between the EEC and LADD Syndromes.

17p13.3 Genomic Rearrangement in a Chinese Family With Split-Hand/Foot Malformation With Long Bone Deficiency: Report of a Complicated Duplication With Marked Variation in Phenotype

A Novel Heterozygous Intragenic Sequence Variant in DLX6 Probably Underlies First Case of Autosomal Dominant Split-Hand/Foot Malformation Type 1

Fine Mapping of the Split-Hand/Split-Foot Locus (SHFM3) at 10q24: Evidence for Anticipation and Segregation Distortion

Phenotypic and Genetic Characterization of a Patient With a De Novo Interstitial 14q24.1q24.3 Deletion