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相似文献
1
Partial albinism.部分白化病
JAMA. 1966 Feb 14;195(7):519-23.
2
[Partial familial albinism (piebaldism): ultrastructural study].
Ann Dermatol Syphiligr (Paris). 1970;97(3):267-86.
3
[Partial familial piebaldism (father and son)].
Bull Soc Fr Dermatol Syphiligr. 1969;76(2):149-50.
4
Macromelanosomes in X-linked ocular albinism (XLOA).X连锁性眼白化病（XLOA）中的巨大黑素小体
Acta Derm Venereol. 1985;65(1):66-9.
5
X-linked ocular albinism: relative value of skin biopsy, iris transillumination and funduscopy in identifying affected males and carriers.
Can J Ophthalmol. 1981 Jul;16(3):121-3.
6
[Piebaldism (partial albinism): apropos of 2 cases].
Dermatologica. 1977;155(3):185-9.
7
[Albinism and other genetically determined generalized, or patchy disseminated hypopigmentations of the skin].
Hautarzt. 1982 Feb;33(2):89-95.
8
Hereditary puzzles in albinism: heterogeneity or phenotypical variation?
Trans Ophthalmol Soc U K (1962). 1983;103 ( Pt 3):318-30.
9
X-linked inheritance of ocular albinism with late-onset sensorineural deafness.
Am J Med Genet. 1984 Dec;19(4):797-803. doi: 10.1002/ajmg.1320190421.
10
Partial albinism and immunodeficiency: ultrastructural study of haemophagocytosis and bone marrow erythroblasts in one case.
Pathol Res Pract. 1980 May;167(1):151-65. doi: 10.1016/S0344-0338(80)80186-5.
引用本文的文献
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Cellular and ultrastructural characterization of the grey-morph phenotype in southern right whales (Eubalaena australis).南露脊鲸（Eubalaena australis）灰色形态表型的细胞和超微结构特征
PLoS One. 2017 Feb 7;12(2):e0171449. doi: 10.1371/journal.pone.0171449. eCollection 2017.
2
Allelic Mutations of KITLG, Encoding KIT Ligand, Cause Asymmetric and Unilateral Hearing Loss and Waardenburg Syndrome Type 2.编码KIT配体的KITLG基因的等位基因突变导致不对称性单侧听力损失和2型瓦登伯革氏综合征。
Am J Hum Genet. 2015 Nov 5;97(5):647-60. doi: 10.1016/j.ajhg.2015.09.011. Epub 2015 Oct 29.
3
Clinical and laboratory diagnosis in disorders of pigmentation.色素沉着紊乱的临床与实验室诊断
J Natl Med Assoc. 1966 Nov;58(6):410-2.
4
[Studies on albumin].[关于白蛋白的研究]
Arch Dermatol Forsch. 1971;240(2):123-37.
5
Dominant piebald trait (white forelock and leukoderma) with neurological impairment.具有神经功能障碍的显性花斑性状（白色额发和白斑病）
Am J Hum Genet. 1971 Jul;23(4):383-9.
6
[Ultrastructure of white leaf-shaped macules in tuberous sclerosis (author's transl)].
Arch Dermatol Forsch. 1973;248(1):13-27.
7
[The Langerhans cells. Results of newer experimental studies. II].[朗格汉斯细胞。最新实验研究结果。II]
Arch Klin Exp Dermatol. 1967;229(1):76-101.
8
Homozygosity in piebald trait.花斑性状的纯合性。
J Med Genet. 1987 Sep;24(9):568-71. doi: 10.1136/jmg.24.9.568.
9
10
Mast cells in the epidermis of piebaldism.
Arch Dermatol Forsch. 1975;251(3):221-5. doi: 10.1007/BF00561763.
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