| P2093 | author name string | D. B. Windhorst | |
| | G. Padgett | |
| P2860 | cites work | Racial Differences in the Fate of Melanosomes in Human Epidermis | Q28256038 |
| | Abnormal bactericidal, metabolic, and lysosomal functions of Chediak-Higashi Syndrome leukocytes | Q28363269 |
| | Defective Granulocyte Regulation in the Chediak–Higashi Syndrome | Q33472538 |
| | Congenital gigantism of peroxidase granules; the first case ever reported of qualitative abnormity of peroxidase. | Q34537537 |
| | Comparative studies of the Chediak-Higashi syndrome | Q35972807 |
| | Differences in enzyme content of azurophil and specific granules of polymorphonuclear leukocytes. I. Histochemical staining of bone marrow smears | Q36189957 |
| | Differences in enzyme content of azurophil and specific granules of polymorphonuclear leukocytes. II. Cytochemistry and electron microscopy of bone marrow cells | Q36189970 |
| | Resolution of granules from rabbit heterophil leukocytes into distinct populations by zonal sedimentation | Q36190289 |
| | Origin of granules in polymorphonuclear leukocytes. Two types derived from opposite faces of the Golgi complex in developing granulocytes | Q41078473 |
| | Aleutian disease of mink: properties of the etiologic agent and the host responses | Q45250479 |
| | Neuropathological changes in Chédiak-Higashi disease | Q49084784 |
| | Cytochemical and Genetic Studies in Four Cases of Chediak-Higashi-Steinbrinck Syndrome | Q53759278 |
| | Granulocyte chemotaxis in the Chediak-Higashi syndrome of mink | Q54341214 |
| | Phagocytosis in chronic granulomatous disease and the Chediak-Higashi syndrome | Q67267623 |
| | The Chediak-Higashi syndrome: electrophysiological and electron microscopic observations on the peripheral neuropathy | Q68565983 |
| | A human pigmentary dilution based on a heritable subcellular structural defect--the Chediak-Higashi syndrome | Q70081467 |
| | Giant granules in leukocytes of the beige mouse | Q71881427 |
| | Fatal (chronic) granulomatous disease of childhood: a hereditary defect of leukocyte function | Q72073331 |
| | Alteration of Sphingolipid Metabolism in Leukocytes from Patients with the Chediak–Higashi Syndrome | Q72074076 |
| | The Chediak-Higashi syndrome: formation of giant melanosomes and the basis of hypopigmentation | Q72357437 |
| | Genetic variations in the fine structure and ontogeny of mouse melanin granules | Q72757315 |
| | Chediak-Higashi syndrome: hereditary gigantism of cytoplasmic organelles | Q72774115 |
| | CHEDIAK-HIGASHI SYNDROME. CYTOLOGIC AND SERUM LIPID OBSERVATIONS IN A CASE AND FAMILY | Q76799579 |
| | A CYTOLOGICAL AND CYTOCHEMICAL STUDY OF CHEDIAK'S LEUKOCYTIC ANOMALY | Q76997257 |
| | Chédiak and Higashi's Disease. Probable Identity of “A New Leucocytal Anomaly (Chédiak)” and “Congenital Gigantism of Peroxidase Granules (Higashi)” | Q78748824 |
| | THE CHEDIAK-HIGASHI ANOMALY AND THE ALEUTIAN TRAIT IN MINK: HOMOLOGOUS DEFECTS OF LYSOSOMAL STRUCTURE | Q113794164 |
| P433 | issue | 6 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | biochemistry | Q7094 |
| | cell biology | Q7141 |
| | dermatology | Q171171 |
| | Chediak-Higashi syndrome | Q934034 |
| | animal disease model | Q64732998 |
| P304 | page(s) | 529-537 | |
| P577 | publication date | 1973-06-01 | |
| P1433 | published in | Journal of Investigative Dermatology | Q3186921 |
| P1476 | title | The Chediak-Higashi Syndrome and the Homologous Trait in Animals | |
| P478 | volume | 60 | |