A novel X-linked dominant condition: X-linked congenital isolated ptosis

American Journal of Human Genetics

Volumn 66, Issue 4, 2000, Pages 1455-1460

  McMullan, Tristan F W ^a   Collins, Andrew R ^b   Tyers, Anthony G ^a   Robinson, David O ^a  

^a SALISBURY DISTRICT HOSPITAL   (United Kingdom)

^b UNIVERSITY OF SOUTHAMPTON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME XQ; FEMALE; GENE LOCUS; GENETIC LINKAGE; HUMAN; HUMAN TISSUE; MALE; PHENOTYPE; PRIORITY JOURNAL; PTOSIS; X CHROMOSOME DOMINANT INHERITANCE;

EID: 0033911791     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302860     Document Type: Article

References (9)

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3. Engle EC, Castro AE, Macy ME, Knoll JHM, Beggs AH (1997) A gene for isolated congenital ptosis maps to a 3 cM region within 1p32-p34.1. Am J Hum Genet 60:1150-1157
4. O'Connell JR, Weeks DE (1995) The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set - recording and fuzzy inheritance. Nat Genet 11:402-408
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