Aquaron R, Lund P, Baker C
Med Trop Sante Int. 2024; 3(4).
PMID: 38390024
PMC: 10879893.
DOI: 10.48327/mtsi.v3i4.2023.434.
Kromberg J, Flynn K, Kerr R
Invest Ophthalmol Vis Sci. 2023; 64(10):14.
PMID: 37440261
PMC: 10353740.
DOI: 10.1167/iovs.64.10.14.
Mason C, Guillery R
Eur J Neurosci. 2019; 49(7):913-927.
PMID: 30801828
PMC: 6697109.
DOI: 10.1111/ejn.14396.
Young A, Powelson E, Whitney I, Raven M, Nusinowitz S, Jiang M
Invest Ophthalmol Vis Sci. 2008; 49(7):3245-52.
PMID: 18378571
PMC: 2881626.
DOI: 10.1167/iovs.08-1806.
Summers C
Trans Am Ophthalmol Soc. 1996; 94:1095-155.
PMID: 8981720
PMC: 1312119.
Hermansky-Pudlak syndrome: albinism with lipofuscin storage.
Fagadau W, Heinemann M, COTLIER E
Int Ophthalmol. 1981; 4(1-2):113-22.
PMID: 7298260
DOI: 10.1007/BF00139585.
Allelism in human oculocutaneous albinism.
Warren S
Am J Hum Genet. 1981; 33(3):479-80.
PMID: 6787918
PMC: 1685037.
Albinism: phenotype or genotype?.
van Dorp D, van Haeringen N, DELLEMAN J, Apkarian P, Westerhof W
Doc Ophthalmol. 1983; 56(1-2):183-94.
PMID: 6420133
DOI: 10.1007/BF00154728.
Amish albinism: a distinctive autosomal recessive phenotype.
Nance W, Jackson C, WITKOP Jr C
Am J Hum Genet. 1970; 22(5):579-86.
PMID: 5516239
PMC: 1706616.
Genetic linkage analysis of human hemoglobin variants.
Nance W, Conneally M, Kang K, Reed T, Schroder J, Rose S
Am J Hum Genet. 1970; 22(4):453-9.
PMID: 5432289
PMC: 1706597.
Genetical aspects of severe visual impairment in childhood.
Fraser G
J Med Genet. 1970; 7(3):257-67.
PMID: 5312664
PMC: 1468872.
DOI: 10.1136/jmg.7.3.257.
Linkage between a hemoglobin locus and albinism in the Norway rat.
French E, Roberts K, SEARLE A
Biochem Genet. 1971; 5(4):397-404.
PMID: 5096391
DOI: 10.1007/BF00485864.
Studies of platelets in a variant of the Hermansky-Pudlak syndrome.
White J, Edson J, Desnick S, WITKOP Jr C
Am J Pathol. 1971; 63(2):319-32.
PMID: 5090642
PMC: 2047499.
Mapping the gene for X-linked cataracts and microcornea with facial, dental, and skeletal features to Xp22: an appraisal of the Nance-Horan syndrome.
Lewis R
Trans Am Ophthalmol Soc. 1989; 87:658-728.
PMID: 2576480
PMC: 1298561.
Temperature-sensitive tyrosinase associated with peripheral pigmentation in oculocutaneous albinism.
King R, Townsend D, Oetting W, Summers C, Olds D, White J
J Clin Invest. 1991; 87(3):1046-53.
PMID: 1900307
PMC: 329899.
DOI: 10.1172/JCI115064.
Progress in screening for inborn errors of metabolism.
Watts R
Experientia. 1978; 34(2):143-52.
PMID: 624338
DOI: 10.1007/BF01944644.
The ultrastructure of defective human platelets.
White J, Gerrard J
Mol Cell Biochem. 1978; 21(2):109-28.
PMID: 102916
DOI: 10.1007/BF00240281.