Fehlende Fingerabdrücke und genetische Defekte
Author:
Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/978-3-662-57872-8_9
Reference33 articles.
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2. Adra CN, Donato JL, Badovinac R et al (2000) SMARCAD1, a novel human helicase family-defining member associated with genetic instability: cloning, expression, and mapping to 4q22-q23, a band rich in breakpoints and deletion mutants involved in several human diseases. Genomics 69(2):162–173
3. Baird HW (1964) Kindred showing congenital absence of the dermal ridges (fingerprints) and associated anomalies. J Pediatr 64(5):621–631
4. Bali RS, Chaube R (1994) Application and methodological perspectives in Dermatoglyphics. Northern Book Centre, New Dehli
5. Basan M (1965) Ektodermale Dysplasie – Fehlendes Papillarmuster, Nagelveränderungen und Vierfingerfurche. Arch Klin Exp Dermatol 222(6):546–557
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