Oculocutaneous albinism, immunodeficiency, hematological disorders, and minor anomalies: a new autosomal recessive syndrome?

Dieter Kotzot; K Richter; K Gierth-Fiebig

doi:10.1002/ajmg.1320500303

Oculocutaneous albinism, immunodeficiency, hematological disorders, and minor anomalies: a new autosomal recessive syndrome?

Dieter Kotzot, K Richter, K Gierth-Fiebig

Research output: Contribution to journal › Case report › peer-review

20 Citations (Web of Science)

Original language	English
Pages (from-to)	224-227
Journal	AMERICAN JOURNAL OF MEDICAL GENETICS
Volume	50
Issue number	3
DOIs	https://doi.org/10.1002/ajmg.1320500303
Publication status	Published - 1994

Keywords

HERMANSKY-PUDLAK SYNDROME

Access to Document

10.1002/ajmg.1320500303

Cite this

Kotzot, D., Richter, K., & Gierth-Fiebig, K. (1994). Oculocutaneous albinism, immunodeficiency, hematological disorders, and minor anomalies: a new autosomal recessive syndrome? AMERICAN JOURNAL OF MEDICAL GENETICS , 50(3), 224-227. https://doi.org/10.1002/ajmg.1320500303

Kotzot, Dieter ; Richter, K ; Gierth-Fiebig, K. / Oculocutaneous albinism, immunodeficiency, hematological disorders, and minor anomalies: a new autosomal recessive syndrome?. In: AMERICAN JOURNAL OF MEDICAL GENETICS 1994 ; Vol. 50, No. 3. pp. 224-227.

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title = "Oculocutaneous albinism, immunodeficiency, hematological disorders, and minor anomalies: a new autosomal recessive syndrome?",

keywords = "HERMANSKY-PUDLAK SYNDROME",

author = "Dieter Kotzot and K Richter and K Gierth-Fiebig",

year = "1994",

doi = "10.1002/ajmg.1320500303",

language = "English",

volume = "50",

pages = "224--227",

journal = "AMERICAN JOURNAL OF MEDICAL GENETICS ",

issn = "0148-7299",

number = "3",

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