Extracutaneous analogies of Blaschko lines

American Journal of Medical Genetics

Volumn 85, Issue 4, 1999, Pages 338-341

  Rott, Hans Dieter ^a  

^a UNIVERSITY OF ERLANGEN NUREMBERG   (Germany)

Author keywords

Blaschko line analogies; Incontinentia pigmenti Bloch Sulzberger; Osteopathia striata with cranial sclerosis; X chromosome inactivation; X linked amelogenesis imperfecta; X linked cataracts; X linked ocular albinism

Indexed keywords

ALBINISM; AMELOGENESIS IMPERFECTA; ARTICLE; BONE DISEASE; CATARACT; HETEROZYGOTE; HUMAN; INCONTINENTIA PIGMENTI; MOSAICISM; PRIORITY JOURNAL; SOMATIC MUTATION; X CHROMOSOME; X CHROMOSOME INACTIVATION;

ADULT; BONE DISEASES; BRAIN; DOSAGE COMPENSATION, GENETIC; EYE DISEASES, HEREDITARY; FEMALE; GENETIC DISEASES, INBORN; HETEROZYGOTE; HUMANS; INCONTINENTIA PIGMENTI; LINKAGE (GENETICS); MOSAICISM; X CHROMOSOME;

EID: 0032771724     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19990806)85:4<338::AID-AJMG5>3.0.CO;2-8     Document Type: Article

References (17)

1. Behninger C. 1998. Klinik und Genetik der Osteopathia striata mit cranialer Sklerose. Medical thesis, University of Erlangen-Nuremberg, Germany (in preparation).
2. Blaschko A. 1901. Die Nervenverteilung in der Haut in ihrer Beziehung zu den Erkrankungen der Haut. Braumüller: Wien & Leipzig.
3. Born G, Grützner P, Henninger H. 1976. Evidenz für eine Mosaikstruktur der Netzhaut bei Konduktorinnen für Dichromasie. Humangenetik 32: 189-196.
4. Happle R. 1978. Genetische Interpretation streifenförmiger Hautanomalien. Hautarzt 29:357-363.
5. Happle R, Küchle HJ. 1983. Sectorial cataract: a possible example of Lyonisation. Lancet 1:919-920.
6. Happle R, Phillips RJS, Roessner A, Jünemann G. 1983. Homologous genes for X-linked chondrodysplasia punctata in man and mouse. Hum Genet 63:24-27.
7. Hussels I. 1971. X-linked cataract: Two pedigrees. Birth Defects Orig Artic Ser 7:164-165.
8. Jaeger Ch, Jay B. 1981. X-linked ocular albinism: a family containing a manifesting heterozygote, and an affected male married to a female with autosomal recessive ocular albinism. Hum Genet 56:299-304.
9. Jaenisch R. 1985. Mammalian neural crest cells participate in normal embryonic development on microinjection into post-implantation mouse embryos. Nature 318:181-183.
10. Knudson AG. 1971. Mutation and human cancer: statistical study of retinoblastoma. Proc Natl Acad Sci USA 68:820-823.
11. Koniszewski G, Rott HD. 1985. Der Lyon-Effekt an der Linse: Konduktorinnenbefunde bei X-chromosomal gebundener Katarakt und beim Lowe Syndrom. Klin Mbl Augenheilk 187:525-528.
12. Lang G, Rott HD, Pfeiffer RA. 1990. X-linked ocular albinism: Characteristic pattern of affection in female carriers. Ophthalmic Pediatr 11: 265-271.
13. Lyon M. 1962. Sex chromatin and gene action in the mammalian X-chromosome. Am J Hum Genet 14:135-148.
14. Online Mendelian Inheritance in Man, OMIM (TM). 1998. Center for Medical Genetics, John Hopkins University (Baltimore, MD) and National Center for Biotechnology Information, National Library of Medicine (Bethesda, MD).
15. Rott HD. 1984. Partial sweat gland aplasia in incontinentia pigmenti Bloch-Sulzberger: implications for nosologic classification. Clin Genet 26:36-38.
16. Rott HD, Lang GE, Huk W, Pfeiffer RA. 1990. Hypomelanosis of Ito (incontinentia pigmenti achromians): ophthalmologic evidence for somatic mosaicism. Ophthalmic Pediatr 11:273-279.
17. Schulze C. 1987. Anomalien und Mißbildungen der menschlichen Zähne. Berlin-Chicago-London-Sao Paulo-Tokio: Quintessenz Verlags-GmbH. p 453-500.