H. Rott

A microdeletion of less than 250 kb, including the proximal part of the FMR-I gene and the fragile-X site, in a male with the clinical phenotype of fragile-X syndrome.

Doris Wöhrle, Dieter Kotzot, Mark C. Hirst et al. · PubMed · 1992 · 173 citations

Life Sciences, Genetics, Molecular Genetics +11

Identification of eight novel coagulation factor XIII subunit A mutations: implied consequences for structure and function

Vytautas Ivaškevičius, Arijit Biswas, Carville G. Bevans et al. · Haematologica · 2010 · 46 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Multiplate^®Whole Blood Impedance Point of Care Aggregometry: Preliminary Reference Values in Healthy Infants, Children and Adolescents

Susan Halimeh, Giulia De Angelis, Anton Sander et al. · Klinische Pädiatrie · 2010 · 46 citations

Medicine, Hematology, Pediatrics +17

Mutations affecting disulphide bonds contribute to a fairly common prevalence of <i>F13B</i> gene defects: results of a genetic study in 14 families with factor XIII B deficiency

Vytautas Ivaškevičius, Arijit Biswas, Ralph M. Loreth et al. · Haemophilia · 2010 · 33 citations

Life Sciences, Genetics, Molecular Genetics +17

Contraception, venous thrombosis and biological plausability.

H. Rott · PubMed · 2013 · 19 citations

Medicine, Endocrinology, Gynecology +14