B. Heye

发表

Cortically evoked motor responses in patients with Xp22.3‐linked Kallmann's syndrome and in female gene carriers

A Danek, A. Danek, B. Heye, 1992, Annals of neurology.

Kallman syndrome versus idiopathic hypogonadotropic hypogonadism at MR imaging.

T. Vogl, A. Danek, R. Felix, 1994, Radiology.

Definitive localization of X-linked Kallman syndrome (hypogonadotropic hypogonadism and anosmia) to Xp22.3: close linkage to the hypervariable repeat sequence CRI-S232.

A. Ballabio, T. Meitinger, C. Petit, 1990, American journal of human genetics.

Olfactory function in patients with hypogonadotropic hypogonadism: an all-or-none phenomenon?

A. Danek, J. Schopohl, M. Laska, 1994, Chemical senses.

Truncation of the Down syndrome candidate gene DYRK1A in two unrelated patients with microcephaly.

Reinhard Ullmann, Zeynep Tümer, Niels Tommerup, 2008, American journal of human genetics.

Intragenic Deletion of theKALIG-1Gene in Kallmann's Syndrome

A. Ballabio, T. Meitinger, D. Bick, 1992 .

Copy-number variations measured by single-nucleotide-polymorphism oligonucleotide arrays in patients with mental retardation.

V. Liebscher, T. Meitinger, T. Strom, 2007, American journal of human genetics.

UMODL1/Olfactorin is an extracellular membrane‐bound molecule with a restricted spatial expression in olfactory and vomeronasal neurons

E. Rugarli, Elena Riaño, P. Bazzicalupo, 2005, The European journal of neuroscience.

The breakpoint identified in a balanced de novo translocation t(7;9)(p14.1;q31.3) disrupts the A-kinase (PRKA) anchor protein 2 gene (AKAP2) on chromosome 9 in a patient with Kallmann syndrome and bone anomalies.

E. Rugarli, R. Ravazzolo, T. Meitinger, 2007, International journal of molecular medicine.

Brief report: intragenic deletion of the KALIG-1 gene in Kallmann's syndrome.

A. Ballabio, T. Meitinger, D. Bick, 1992, The New England journal of medicine.