Wolcott‐Rallison syndrome in two siblings with isolated central hypothyroidism

EIF2AK3, encoding translation initiation factor 2-α kinase 3, is mutated in patients with Wolcott-Rallison syndrome

2000 • 800 citations

Further evidence for an imprinted gene for neonatal diabetes localised to chromosome 6q22-q23

1996 • 145 citations

Infancy-onset diabetes mellitus and multiple epiphyseal dysplasia

1972 • 141 citations

Wolcott-Rallison syndrome: Diabetes mellitus and spondyloepiphyseal dysplasia

1982 • 72 citations

Suppression of a mitochondrial tRNA gene mutation phenotype associated with changes in the nuclear background

1999 • 65 citations

Autopsy Findings in the Wolcott-Rallison Syndrome

1997 • 63 citations

Paternal uniparental disomy for chromosome 6 causes transient neonatal diabetes.

1997 • 49 citations

Wolcott-Rallison syndrome

1995 • 46 citations

Parallel molecular genetic analysis

1998 • 41 citations

Transient Neonatal Diabetes mellitus in a Child with invdup(6)(q22q23) of Paternal Origin

1997 • 29 citations

Wolcott‐Rallison syndrome associated with congenital malformations and a mosaic deletion 15q 11–12

1996 • 26 citations

Wolcott-Rallison Syndrome: Clinical, Radiological and Histological Findings in a Saudi Child

2001 • 22 citations

Organisation of the human PAX4 gene and its exclusion as a candidate for the Wolcott-Rallison syndrome.

1998 • 18 citations