I. Hansmann

Homologous sequences at human chromosome 9 bands p12 and q13-21.1 are involved in different patterns of pericentric rearrangements

Heike Starke, Jörg Seidel, Wolfram Henn et al. · European Journal of Human Genetics · 2002 · 204 citations

Chromatin, Pericentric Rearrangements, Genetic Disorder +10

Molecular structure and chromosomal mapping of the human homolog of the agouti gene.

H Y Kwon, Scott J. Bultman, C. Löffler et al. · Proceedings of the National Academy of Sciences · 1994 · 159 citations · Full text

Genetics, Human Polymorphism, Gene Characterization +18

High Frequency of Mosaicism among Patients with Neurofibromatosis Type 1 (NF1) with Microdeletions Caused by Somatic Recombination of the JJAZ1 Gene

Hildegard Kehrer‐Sawatzki, Lan Kluwe, Catharina Sandig et al. · The American Journal of Human Genetics · 2004 · 139 citations · Full text

Jjaz1 Gene, Mendelian Disorder, Genetic Disorder +8

Duplication of Xq26.2-q27.1, includingSOX3, in a mother and daughter with short stature and dyslalia

Paweł Stankiewicz, Hannelore Thiele, Mike Schlicker et al. · American Journal of Medical Genetics Part A · 2005 · 118 citations

20p12.3 microdeletion predisposes to Wolff–Parkinson–White syndrome with variable neurocognitive deficits

Seema R. Lalani, Joseph V. Thakuria, Gerald F. Cox et al. · Journal of Medical Genetics · 2008 · 109 citations · Full text