Adult syndrome allelic to limb mammary syndrome (LMS)?

American Journal of Medical Genetics

Volumn 90, Issue 2, 2000, Pages 179-182

  Propping, Peter ^a,c   Friedl, Waltraut ^a   Wienker, Thomas F ^a   Uhlhaas, Siegfried ^a   Zerres, Klaus ^b  

^a UNIVERSITY OF BONN   (Germany)

^b RWTH AACHEN UNIVERSITY   (Germany)

^c UNIVERSITY HOSPITAL BONN   (Germany)

Author keywords

ADULT syndrome; Ectrodactyly; Limb mammary syndrome; Mammary gland hypoplasia

Indexed keywords

ALLELE; ANHIDROSIS; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BREAST HYPOPLASIA; CLEFT PALATE; ECTRODACTYLY; FEMALE; GENE MAPPING; GERMANY; HUMAN; HYPODONTIA; MALE; NAIL DYSPLASIA; PRIORITY JOURNAL; SYNDACTYLY;

ABNORMALITIES, MULTIPLE; ADULT; ALLELES; BREAST; CHILD; CHROMOSOMES, HUMAN, PAIR 3; FEMALE; GENOTYPE; HUMANS; LIMB DEFORMITIES, CONGENITAL; LINKAGE (GENETICS); MALE; PEDIGREE; SYNDROME;

EID: 0034677218     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(20000117)90:2<179::AID-AJMG21>3.0.CO;2-M     Document Type: Article

References (9)

1. Endo T, Imanishi T, Gojobori T, Inoko H. 1997. Evolutionary significance of intra-genome duplications on human chromosomes. Gene 205:19-27.
2. Hamel B, Smits A, van Beersum S, Hoekstra H, Mariman E, Tuerlings J, van Buggenhout G, Brunner H, Ropers HH. 1996. A large family with limb-mammary syndrome: clinical and molecular findings. Eur J Hum Genet Suppl 4:148.
3. Lathrop GM, Lalouel JM, Julier C, Ott J. 1984. Strategies for multilocus linkage analysis in humans. Proc Natl Acad Sci USA 81:3443-3446.
4. Lundin LG. 1993. Evolution of the vertebrate genome as reflected in paralogous chromossomal regions in man and the house mouse. Genomics 16:1-19.
5. Marshfield map. http://www.marshmed.org/genetics/
6. Miller SA, Dykes DD, Polesky HF. 1988. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 16: 1215.
7. O'Quinn JR, Hennekam RC, Jorde LB, Bamshad M. 1998. Syndromic ectrodactyly with severe limb, ectodermal, urogenital, and palatal defects maps to chromosome 19. Am J Hum Genet 62:130-135.
8. Propping P, Zerres K. 1993. ADULT syndrome: An autosomal-dominant disorder with pigment anomalies, ectrodactyly, nail dysplasia, and hypodontia. Am J Med Genet 45:642-648.
9. Van Bokhoven H, Jung M, Smits APT, van Beersum S, Rüschendorf F, van Steensel M, Veenstra M, Tuerlings JHAM, Mariman ECM, Brunner HG, Wienker TF, Reis A, Ropers HH, Hamel BCJ . 1999. Limb mammary syndrome: a new genetic disorder with mammary hypoplasia, ectrodactyly, and other hand/foot anomalies map to human chromosome 3q27. Am J Hum Genet 64:538-546.