Closing in on the Rieger syndrome gene on 4q25: Mapping translocation breakpoints within a 50-kb region

American Journal of Human Genetics

Volumn 59, Issue 6, 1996, Pages 1297-1305

  Datson, Nicole A ^b   Semina, Elena ^b   Van Staalduinen, André A A ^b   Dauwerse, Hans G ^b   Meershoek, Eric J ^b   Heus, Joris J ^b   Frants, Rune R ^b   Den Dunnen, Johan T ^a   Murray, Jeffrey C ^b   Van Ommen, Gert Jan B ^b  

^a LEIDEN UNIVERSITY   (Netherlands)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

DNA; EPIDERMAL GROWTH FACTOR;

ARTICLE; CHROMOSOME 4Q; CHROMOSOME TRANSLOCATION 4; CONTROLLED STUDY; COSMID; FLUORESCENCE IN SITU HYBRIDIZATION; GENE; GENE MAPPING; HUMAN; HUMAN CELL; KARYOTYPE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RIEGER SYNDROME; SOUTHERN BLOTTING; YEAST ARTIFICIAL CHROMOSOME;

BLOTTING, SOUTHERN; CELL LINE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 4; CRANIOFACIAL ABNORMALITIES; GLAUCOMA; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; POLYMERASE CHAIN REACTION; SYNDROME; TOOTH ABNORMALITIES; TRANSLOCATION, GENETIC; UMBILICUS;

EID: 19244364120     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (7)

1. Alkemade PPH (1969) Dysgenesis mesodermalis of the iris and the cornea: a study of Rieger's syndrome and Peter's anomaly. PhD thesis, Leiden University, Leiden
2. Buetow KH, Weber JL, Ludwigsen S, Sherpbier-Heddema T, Duyk GM, Sheffield VC, Wang Z, et al (1994) Integrated human genome-wide maps constructed using the CEPH reference panel. Nat Genet 6:391-393
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5. Semina EV, Datson NA, Leysens NJ, Zabel BU, Carey JC, Bell GI, Bitoun P, et al (1996) Exclusion of epidermal growth factor and high-resolution physical mapping across the Rieger syndrome locus. Am J Hum Genet 59:1288-1296 (in this issue)
6. Slavkin HC (1993) Rieger syndrome revisited: experimental approaches using pharmacologic and antisense strategies to abrogate EGF and TGF-alpha functions resulting in dysmorphogenesis during embryonic mouse craniofacial morphogenesis. Am J Med Genet 47:689-697
7. Vaux C, Sheffield L, Keith CG, Voullaire L (1992) Evidence that Rieger syndrome maps to 4q25 or 4q27. J Med Genet 29:256-258