A genetically heterogeneous disorder caused by hypothalamic GNRH deficiency and OLFACTORY NERVE defects. It is characterized by congenital HYPOGONADOTROPIC HYPOGONADISM and ANOSMIA, possibly with additional midline defects. It can be transmitted as an X-linked (GENETIC DISEASES, X-LINKED), an autosomal dominant, or an autosomal recessive trait
A genetically heterogeneous disorder caused by hypothalamic GNRH deficiency and OLFACTORY NERVE defects. It is characterized by congenital HYPOGONADOTROPIC HYPOGONADISM and ANOSMIA, possibly with additional midline defects. It can be transmitted as an X-linked (GENETIC DISEASES, X-LINKED), an autosomal dominant, or an autosomal recessive trait
A genetically heterogeneous disorder caused by hypothalamic GNRH deficiency and OLFACTORY NERVE defects. It is characterized by congenital HYPOGONADOTROPIC HYPOGONADISM and ANOSMIA, possibly with additional midline defects. It can be transmitted as an X-linked (GENETIC DISEASES, X-LINKED), an autosomal dominant, or an autosomal recessive trait
A genetically heterogeneous disorder caused by hypothalamic GNRH deficiency and OLFACTORY NERVE defects. It is characterized by congenital HYPOGONADOTROPIC HYPOGONADISM and ANOSMIA, possibly with additional midline defects. It can be transmitted as an X-linked (GENETIC DISEASES, X-LINKED), an autosomal dominant, or an autosomal recessive trait
A genetically heterogeneous disorder caused by hypothalamic GNRH deficiency and OLFACTORY NERVE defects. It is characterized by congenital HYPOGONADOTROPIC HYPOGONADISM and ANOSMIA, possibly with additional midline defects. It can be transmitted as an X-linked (GENETIC DISEASES, X-LINKED), an autosomal dominant, or an autosomal recessive trait
A genetically heterogeneous disorder caused by hypothalamic GNRH deficiency and OLFACTORY NERVE defects. It is characterized by congenital HYPOGONADOTROPIC HYPOGONADISM and ANOSMIA, possibly with additional midline defects. It can be transmitted as an X-linked (GENETIC DISEASES, X-LINKED), an autosomal dominant, or an autosomal recessive trait
Kalloch, Isaac, 1831-1887 -- Trials, litigation, etc : Only full report of the trial of Rev. I.S. Kalloch on charge of adultery : complete history of the affair, doings of the church, Kalloch's pulpit defence, arrest, arraignment, trial and result, with accurate portraits of Kalloch and the beautiful lady in black and the lecture room of the Lechmere
källor Athen historia : Augustan and Julio-Claudian Athens : a new epigraphy and prosopography / by Geoffrey C.R. Schmalz
2009
1
källor Bamberg historia : Rewriting Roman history in the Middle Ages : the 'Historia Romana' and the Manuscript Bamberg, Hist. 3 / Marek Thue Kretschmer
2007
1
källor Europa intellektuellt liv historia : Locations of knowledge in medieval and early modern Europe : esoteric discourse and Western identities / by Kocku von Stuckrad
källor Rom historia verk före 1800 : Rewriting Roman history in the Middle Ages : the 'Historia Romana' and the Manuscript Bamberg, Hist. 3 / Marek Thue Kretschmer
2007
1
källor Rom historiografi historia : Rewriting Roman history in the Middle Ages : the 'Historia Romana' and the Manuscript Bamberg, Hist. 3 / Marek Thue Kretschmer
Kalman filtering -- Data processing : Introduction to random signals and applied Kalman filtering : with MATLAB exercises / Robert Grover Brown, Patrick Y.C. Hwang
Kalman, Tibor. : Tibor Kalman : perverse optimist / edited by Peter Hall and Michael Bierut ; essays by Kurt Andersen, Steven Heller, and Rick Poynor ; contributions by Paola Antonelli ... [and others]
1998
1
Kalmanovitch, Zelig, 1885-1944. : The tragedy of a generation : the rise and fall of Jewish nationalism in Eastern Europe / Joshua M. Karlip
