RXR alpha deficiency confers genetic susceptibility for aortic sac, conotruncal, atrioventricular cushion, and ventricular muscle defects in mice.

Function of the retinoic acid receptors (RARs) during development: (II) Multiple abnormalities at various stages of organogenesis in RAR double mutants

1994 • 987 citations

An analysis of the syndrome of malformations induced by maternal vitamin a deficiency. Effects of restoration of vitamin a at various times during gestation

1953 • 754 citations

Genetic analysis of RXRα developmental function: Convergence of RXR and RAR signaling pathways in heart and eye morphogenesis

1994 • 684 citations

RXR alpha mutant mice establish a genetic basis for vitamin A signaling in heart morphogenesis.

1994 • 632 citations

Function of retinoic acid receptor γ in the mouse

1993 • 595 citations

High postnatal lethality and testis degeneration in retinoic acid receptor alpha mutant mice.

1993 • 541 citations

The elastin gene is disrupted by a translocation associated with supravalvular aortic stenosis

1993 • 419 citations

The Clinical and Genetic Spectrum of the Holt-Oram Syndrome (Heart-Hand Syndrome)

1994 • 383 citations

A deletion in chromosome 22 can cause digeorge syndrome

1981 • 366 citations

Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11.

1993 • 267 citations

Aortic‐arch and cardiac anomalies in the offspring of vitamin A deficient rats

1949 • 254 citations

A mutant p53 transgene accelerates tumour development in heterozygous but not nullizygous p53–deficient mice

1995 • 233 citations

Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects.

1993 • 227 citations

Normal development and growth of mice carrying a targeted disruption of the alpha 1 retinoic acid receptor gene.

1993 • 192 citations

Atrial-like phenotype is associated with embryonic ventricular failure in retinoid X receptor alpha -/- mice.

1995 • 166 citations

Cloning a balanced translocation associated with DiGeorge syndrome and identification of a disrupted candidate gene

1995 • 159 citations

Retinoic Acid Receptor β2 (RARβ2) Null Mutant Mice Appear Normal

1994 • 141 citations

Toward a Molecular Understanding of Congenital Heart Disease

1995 • 139 citations

Wholemount in situ hybridization of vertebrate embryos

1992 • 78 citations

Retinoic Acid Embryopathy

1986 • 70 citations

Prenatal development of the endocardium: a review.

1981 • 44 citations

Variations in Microscopic Anatomy and Ultrastructure of Human Embryonic Hearts Subjected to Three Different Modes of Fixation

1990 • 33 citations

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