A mutation in a skin-specific isoform of SMARCAD1 causes autosomal-dominant adermatoglyphia.

[1]  P. Itin,et al.  The immigration delay disease: adermatoglyphia-inherited absence of epidermal ridges. , 2011, Journal of the American Academy of Dermatology.

[2]  A. R. Ennos,et al.  Fingerprints are unlikely to increase the friction of primate fingerpads , 2009, Journal of Experimental Biology.

[3]  G. Debrégeas,et al.  The Role of Fingerprints in the Coding of Tactile Information Probed with a Biomimetic Sensor , 2009, Science.

[4]  Osamu Ohara,et al.  The novel protein complex with SMARCAD1/KIAA1122 binds to the vicinity of TSS. , 2008, Journal of molecular biology.

[5]  J. Lugassy,et al.  Naegeli-franceschetti-jadassohn Syndrome and Dermatopathia Pigmentosa Reticularis: Two Allelic Ectodermal Dysplasias Caused by Dominant Mutations in Krt14 , 2022 .

[6]  T. Cooper,et al.  Minigene reporter for identification and analysis of cis elements and trans factors affecting pre-mRNA splicing. , 2006, BioTechniques.

[7]  T. Reed,et al.  High heritability of fingertip arch patterns in twin‐pairs , 2006, American journal of medical genetics. Part A.

[8]  M. Basan.  Ektodermale Dysplasie , 2004, Archiv für klinische und experimentelle Dermatologie.

[9]  Ravi Sachidanandam,et al.  Intrinsic differences between authentic and cryptic 5' splice sites. , 2003, Nucleic acids research.

[10]  B. Coull,et al.  Effect of prenatal exposure to anticonvulsant drugs on dermal ridge patterns of fingers. , 2002, Teratology.

[11]  Dan Geiger,et al.  Exact genetic linkage computations for general pedigrees , 2002, ISMB.

[12]  S. Weremowicz,et al.  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. , 2000, Genomics.

[13]  Roy Parker,et al.  Mutations in Translation Initiation Factors Lead to Increased Rates of Deadenylation and Decapping of mRNAs inSaccharomyces cerevisiae , 1999, Molecular and Cellular Biology.

[14]  M. Schoor,et al.  Skeletal dysplasias, growth retardation, reduced postnatal survival, and impaired fertility in mice lacking the SNF2/SWI2 family member ETL1 , 1999, Mechanisms of Development.

[15]  N. Elçioglu,et al.  A Rapp-Hodgkin like syndrome in three sibs: clinical, dental and dermatoglyphic study. , 1999, Clinical dysmorphology.

[16]  D A Day,et al.  Post-transcriptional gene regulatory mechanisms in eukaryotes: an overview. , 1998, The Journal of endocrinology.

[17]  M. Límová,et al.  Congenital absence of dermatoglyphs. , 1993, Journal of the American Academy of Dermatology.

[18]  W. Babler.  Embryologic development of epidermal ridges and their configurations. , 1991, Birth defects original article series.

[19]  Absence of dermal ridge patterns: genetic heterogeneity. , 1983, American journal of medical genetics.

[20]  A. Trowbridge,et al.  Dyskeratosis congenita: clinical features and genetic aspects. Report of a family and review of the literature. , 1975, Journal of medical genetics.

[21]  J Verbov,et al.  Clinical significance and genetics of epidermal ridges--a review of dermatoglyphics. , 1970, The Journal of investigative dermatology.

[22]  H. Baird.  Absence of fingerprints in four generations. , 1968, Lancet.

[23]  M. Basan.  [Ectodermal dysplasia. Missing papillary pattern, nail disorders and furrows on 4 fingers]. , 1965, Archiv fur klinische und experimentelle Dermatologie.