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Genetic and Clinical Study of Patients With Xeroderma Pigmentosum, Cockayne Syndrome, or Trichothiodystrophy
This study is currently recruiting participants.
Study NCT00004044 Information provided by National Cancer Institute (NCI)
First Received: December 10, 1999 Last Updated: June 16, 2009
History of Changes
Related Studies can be found by searching for the Conditions, Interventions, and Sponsors found in this study:
Conditions listed in this trial
Head and Neck Cancer
Intraocular Melanoma
Melanoma (Skin)
Non-Melanomatous Skin Cancer
Precancerous/Nonmalignant Condition
Additional conditions recognized in this trial
Cockayne Syndrome
Eye Neoplasms
Facies
Head and Neck Neoplasms
Ichthyosiform Erythroderma, Congenital
Ichthyosis
Infertility
Melanoma
Mental Retardation
Photosensitivity Disorders
Precancerous Conditions
Skin Neoplasms
Xeroderma Pigmentosum
More general conditions related to this trial
Abnormalities, Multiple
Bone Diseases
Bone Diseases, Developmental
Congenital Abnormalities
Disease Attributes
DNA Repair-Deficiency Disorders
Dwarfism
Eye Diseases
Genetic Diseases, Inborn
Genital Diseases, Female
Genital Diseases, Male
Heredodegenerative Disorders, Nervous System
Infant, Newborn, Diseases
Keratosis
Mental Disorders
Mental Disorders Diagnosed in Childhood
Metabolic Diseases
Musculoskeletal Diseases
Neoplasms
Neoplasms by Histologic Type
Neoplasms by Site
Neoplasms, Germ Cell and Embryonal
Neoplasms, Nerve Tissue
Nervous System Diseases
Neurobehavioral Manifestations
Neurodegenerative Diseases
Neuroectodermal Tumors
Neuroendocrine Tumors
Neurologic Manifestations
Nevi and Melanomas
Pathologic Processes
Pigmentation Disorders
Signs and Symptoms
Skin Abnormalities
Skin Diseases
Skin Diseases, Genetic
Interventions listed in this trial
DNA ploidy analysis
mutation analysis
Sponsors listed in this trial
National Cancer Institute (NCI)
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