X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndrome.

Nutritional supplementation, psychosocial stimulation, and mental development of stunted children: the Jamaican Study

1991 • 682 citations

An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes

1983 • 662 citations

X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus.

1993 • 513 citations

X-linked dilated cardiomyopathy with neutropenia, growth retardation, and 3-methylglutaconic aciduria

1991 • 270 citations

Inherited Cardiomyopathies

1994 • 256 citations

X-Linked Dilated Cardiomyopathy

1987 • 236 citations

A new mtDNA mutation in the tRNALeu(UUR) gene associated with maternally inherited cardiomyopathy

1994 • 181 citations

Identification of a Second Pseudoautosomal Region Near the Xq and Yq Telomeres

1992 • 171 citations

An X-Linked Recessive Cardiomyopathy with Abnormal Mitochondria

1979 • 150 citations

Mapping of the locus for X-linked cardioskeletal myopathy with neutropenia and abnormal mitochondria (Barth syndrome) to Xq28.

1991 • 144 citations

Haemophilia A diagnosis by analysis of a hypervariable dinucleotide repeat within the factor VIII gene

1991 • 142 citations

Barth syndrome: Clinical features and confirmation of gene localisation to distal Xq28

1993 • 117 citations

Analysis of human genetic linkage, revised edition

1993 • 105 citations

Barth syndrome: Clinical observations and genetic linkage studies

1994 • 100 citations

Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 1 of 27)

1991 • 98 citations

Mapping of two genes encoding isoforms of the actin binding protein ABP-280, a dystrophin like protein, to Xq28 and to chromosome 7

1993 • 76 citations

Dilated cardiomyopathy with neutropenia, short stature, and abnormal carnitine metabolism

1988 • 44 citations

Actin-Binding Protein (ABP-280) Filamin Gene (FLN) Maps Telomeric to the Color Vision Locus (R/GCP) and Centromeric to G6PD in Xq28

1993 • 37 citations

Endocardial fibroelastosis: possible X linked inheritance.

1987 • 29 citations

Emery-Dreifuss muscular dystrophy: linkage to markers in distal Xq28.

1993 • 29 citations

Dinucleotide repeat polymorphism in the human X-linked GABA_Areceptora³-subunit gene

1991 • 29 citations

Report of the Fourth International Workshop on Human X Chromosome Mapping 1993 (Part 1 of 4)

1993 • 27 citations

Identification of novel RFLPs in the vicinity of CpG islands in Xq28: application to the analysis of the pattern of X chromosome inactivation.

1992 • 24 citations

Four STR polymorphisms map to a 500 kb region between DXS15 and DXS134

1993 • 23 citations

Dinucleotide repeat polymorphism at Xq26.1 (DXS1114)

1993 • 22 citations

Possible X linked congenital mitochondrial cardiomyopathy in three families.

1993 • 21 citations

Dinucleotide repeat polymorphism close to IDS gene in Xq27.3–q28 (DXS1113)

1993 • 17 citations

Dinucleotide repeat polymorphisms at the DXS294 and DXS300 loci in Xq26

1991 • 11 citations

PCR detection of the Mspl polymorphism in the human IRBP gene (RPB3)

1991 • 3 citations