Ventricular noncompaction and distal chromosome 5q deletion

Isolated noncompaction of left ventricular myocardium. A study of eight cases.

1990 • 1,394 citations

Congenital Heart Disease Caused by Mutations in the Transcription Factor NKX2-5

1998 • 1,284 citations

Isolated Noncompaction of the Myocardium in Adults

1997 • 770 citations

Csx: a murine homeobox-containing gene specifically expressed in the developing heart.

1993 • 533 citations

Cardiac defects and altered ryanodine receptor function in mice lacking FKBP12

1998 • 422 citations

Xq28-linked noncompaction of the left ventricular myocardium: Prenatal diagnosis and pathologic analysis of affected individuals

1997 • 300 citations

Neonatal, Lethal Noncompaction of the Left Ventricular Myocardium Is Allelic with Barth Syndrome

1997 • 298 citations

Heart development inDrosophila and vertebrates: Conservation of molecular mechanisms

1998 • 185 citations

Vertebrate homologs oftinman andbagpipe: Roles of the homeobox genes in cardiovascular development

1998 • 73 citations

Molecular Cloning, Chromosomal Mapping, and Characterization of the Human Cardiac-Specific Homeobox Gene hCsx

1996 • 56 citations

Noncompaction of the ventricular myocardium in Melnick-Needles syndrome

1997 • 49 citations

Assignment of Cardiac Homeobox Gene CSX to Human Chromosome 5q34

1995 • 41 citations

Localization of the Human Mxi1 Transcription Factor Gene (MXI1) to Chromosome 10q24-q25

1994 • 34 citations

Deletion 5q35.3

1994 • 28 citations