Abstract: Disclosed is human genomic DNA having the following STR marker profile: Amel D3S1358 VWA FGA D8S1179 D21S11 D18S51 M 15-17 16-17 21-25 12-14 29-32.2 17-18 D5S818 D13S317 D7S820 CSF1PO TPOX TH01 D16S539 11-12 11-12 8-8 10-11 8-8 7-9.3 10-13 And the use thereof as a reference for studying variations in the human genome that may be associated with certain genetic traits or diseases.

Abstract: A system and method of generating a representation or alteration of a subject. One or more devices may be attached to a subject, and a first signal transmitted towards the subject, the first signal interacting with the one or more devices to produce a second signal. The second signal may be received from the subject and data therein processed. A representation or alteration of the subject may then be generated as a function of the processed data.

Abstract: System and method of for providing haptic feedback to a subject. The method may include providing signals to an electronic interactive device, the device including an array of micro-step motors for contacting a skin surface of the subject and converting the signals to provide input signals to the array of micro-step motors. Haptic feedback may then be provided to the skin surface of the subject in response to the input signals. Exemplary micro-step motors may include two clutching actuators separated by a lateral actuator, each actuator adaptable to operate independently of the other actuators, and a shaft having a motion defined by movement of at least one of the lateral or clutching actuators.

Abstract: A method, system and device for reproducing sound. The device may include an elongated strip of material having a ridge substantially extending the length and width of the elongated strip. The elevation of the ridge may vary along the length of the elongated strip to produce sound when contacted by a wheel of a vehicle travelling substantially along the length of the elongated strip.

Abstract: A method, system and device for reproducing sound. The device may include an elongated strip of material having a ridge substantially extending the length and width of the elongated strip. The elevation of the ridge may vary along the length of the elongated strip to produce sound when contacted by a wheel of a vehicle travelling substantially along the length of the elongated strip.

Abstract: An apparatus for treating a human body with waves, comprising: (i) an inverse wave generating system comprising a substantially rigid, water-tight shell defining a substantially spherical cavity and having a plurality of individual wave generating elements located at predetermined locations on the inner surface thereof and a diameter sufficient to accommodate at least one human body without it contacting the inner surface of the shell or the individual wave generating elements; and (ii) an external frame for positioning the inverse wave generating system relative to the external environment. These apparatus are useful for applying waves to a human body for therapy.

Abstract: Inverse speaker systems comprise a plurality of individual sound-reproducing elements arranged in a substantially spherical arrangement. These inverse speaker systems are useful for applying sound to a human body.

Abstract: Inverse speaker systems comprise a plurality of individual sound-reproducing elements arranged in a substantially spherical arrangement. These inverse speaker systems are useful for applying sound to a human body for therapy.

Abstract: Disclosed is human genomic DNA having the following STR marker profile: Amel D3S1358 VWA FGA D8S1179 D21S11 D18S51 M 15-17 16-17 21-25 12-14 29-32.2 17-18 D5S818 D13S317 D7S820 CSF1PO TPOX TH01 D16S539 11-12 11-12 8-8 10-11 8-8 7-9.3 10-13 And the use thereof as a reference for studying variations in the human genome that may be associated with certain genetic traits or diseases.

Abstract: Disclosed is human genomic DNA having the following STR marker profile: Amel D3S1358 VWA FGA D8S1179 D21S11 M 15–17 16–17 21–25 12–14 29–32.2 D5S818 D13S317 D7S820 CSF1PO TPOX TH01 11–12 11–12 8—8 10–11 8—8 7–9.3 D18S51 17–18 D16S539 10–13 And the use thereof as a reference for studying variations in the human genome that may be associated with certain genetic traits or diseases.