A Submicroscopic Deletion in Xq26 Associated with Familial Situs Ambiguus

Molecular Cloning: A Laboratory Manual

2001 • 133,517 citations

Molecular cloning: A laboratory manual

1990 • 85,659 citations

The Metabolic Basis of Inherited Disease.

1988 • 7,933 citations

Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function

1996 • 3,041 citations

The 1993–94 Généthon human genetic linkage map

1994 • 1,870 citations

The metabolic basis of inherited disease

1995 • 1,007 citations

HNF-3β is essential for node and notochord formation in mouse development

1994 • 985 citations

The winged-helix transcription factor HNF-3β is required for notochord development in the mouse embryo

1994 • 786 citations

A molecular pathway determining left-right asymmetry in chick embryogenesis

1995 • 781 citations

Sequence identification of 2,375 human brain genes

1992 • 764 citations

Nodal is a novel TGF-β-like gene expressed in the mouse node during gastrulation

1993 • 606 citations

Different phenotypes for mice deficient in either activins or activin receptor type II

1995 • 598 citations

Relationship between asymmetric nodal expression and the direction of embryonic turning

1996 • 547 citations

Conserved left–right asymmetry of nodal expression and alterations in murine situs inversus

1996 • 459 citations

Left–right asymmetric expression of the TGFβ-family member lefty in mouse embryos

1996 • 436 citations

Mutations of theConnexin43Gap-Junction Gene in Patients with Heart Malformations and Defects of Laterality

1995 • 376 citations

Human Malformations and Related Anomalies

2015 • 361 citations

Chromosome–specific microsatellite sets for fluorescence–based, semi–automated genome mapping

1994 • 304 citations

Expression of activin subunits, activin receptors and follistatin in postimplantation mouse embryos suggests specific developmental functions for different activins

1994 • 252 citations

Human Malformations and Related Anomalies

1994 • 218 citations

Distinct expression and shared activities of members of the hedgehog gene family of Xenopus laevis

1995 • 200 citations

Mapping a gene for familial situs abnormalities to human chromosome Xq24-q27.1

1993 • 136 citations

Biological asymmetry and handedness

1992 • 105 citations

The Spectrum of Heterotaxic Syndromes

1989 • 103 citations

Molecular characterization of de novo secondary trisomy 13.

1994 • 102 citations

The spectrum of heterotaxic syndromes.

1989 • 102 citations

Disturbance of Morphological Laterality in Humans

2007 • 95 citations

Biological asymmetry and handedness

1991 • 93 citations

X‐linked laterality sequence: Situs inversus, complex cardiac defects, splenic defects

1987 • 77 citations

Embryonic expression and functional analysis of a Xenopus activin receptor

1992 • 63 citations

Failure to Detectconnexin43Mutations in 38 Cases of Sporadic and Familial Heterotaxy

1996 • 60 citations

Heterotaxia syndrome and autosomal dominant inheritance

1995 • 53 citations

Report of the Sixth International Workshop on Human X Chromosome Mapping 1995

1995 • 51 citations

Autosomal dominant transmission of familial laterality defects

1996 • 40 citations

A YAC-based binning strategy facilitating the rapid assembly of cosmid contigs: 1.6 Mb of overlapping cosmids in Xp22

1994 • 33 citations

Absence of mutations in the regulatory domain of the gap junction protein connexin 43 in patients with visceroatrial heterotaxy.

1997 • 31 citations

X‐linked laterality sequence in a family with carrier manifestations

1994 • 30 citations

Asplenia syndrome in a child with a balanced reciprocal translocation of chromosomes 11 and 20 [46,XX,t(11;20)(q13.1;q13.13)]

1996 • 19 citations

YAC/STS Map of 9 Mb of Xq26 at 100-kb Resolution, Localizing 6 ESTs, 6 Genes, and 32 Genetic Markers

1996 • 18 citations

Molecular Cloning ofXenopusActivin Type I Receptor and the Analysis of Its Expression During Embryogenesis

1996 • 11 citations