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Index « ISSN » - entrée « 1537-6605 »
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1537-6591 < 1537-6605 < 1537-744X  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 15.
Ident.Authors (with country if any)Title
000245 (2000) Vandana Shashi ; Margaret N. Berry ; Sarah Shoaf ; James J. Sciote ; Donald Goldstein ; Thomas C. HartA Unique Form of Mental Retardation with a Distinctive Phenotype Maps to Xq26-q27
000819 (2002) Thomas C. Hart ; Yingze Zhang ; Michael C. Gorry ; P. Suzanne Hart [États-Unis] ; Margaret Cooper ; Mary L. Marazita ; Jared M. Marks ; Jose R. Cortelli [Brésil] ; Debora Pallos [Brésil]A Mutation in the SOS1 Gene Causes Hereditary Gingival Fibromatosis Type 1
000E91 (1992) J. Zonana ; M. Jones ; D. Browne ; M. Litt ; P. Kramer ; H. W. Becker ; N. Brockdorff ; S. Rastan ; K. P. Davies ; A. Clarke ; N. S. T. ThomasHigh-resolution mapping of the X-linked hypohidrotic ectodermal dysplasia (EDA) locus
000F53 (1962) Eldon J. GardnerFollow-up Study of a Family Group Exhibiting Dominant Inheritance for a Syndrome Including Intestinal Polyps, Osteomas, Fibromas and Epidermal Cysts
002870 (1990) M. Lagerström ; N. Dahl ; L. Iselius ; B. B Ckman ; U. PetterssonMapping of the gene for X-linked amelogenesis imperfecta by linkage analysis.
007512 (1988) J. Zonana ; A. Clarke ; M. Sarfarazi ; N S Thomas ; K. Roberts ; K. Marymee ; P S HarperX-linked hypohidrotic ectodermal dysplasia: localization within the region Xq11-21.1 by linkage analysis and implications for carrier detection and prenatal diagnosis.
007A80 (1987) T H Beaty ; J A Boughman ; P. Yang ; J A Astemborski ; J B SuzukiGenetic analysis of juvenile periodontitis in families ascertained through an affected proband.
008325 (1972) J C Gall ; A M Stern ; A K Poznanski ; S M Garn ; E D Weinstein ; J R HaywardOto-palato-digital syndrome: comparison of clinical and radiographic manifestations in males and females.
008331 (1972) J. Lichtenstein ; R. Warson ; R. Jorgenson ; J P Dorst ; V A MckusickThe tricho-dento-osseous (TDO) syndrome.
009594 (1993) R C Hennekam ; M. Tilanus ; B C Hamel ; H. Voshart-Van Heeren ; E C Mariman ; S E Van Beersum ; M J Van Den Boogaard ; M H BreuningDeletion at chromosome 16p13.3 as a cause of Rubinstein-Taybi syndrome: clinical aspects.
009717 (1996) M. L. Marazita ; H. Lu ; M. E. Cooper ; S. M. Quinn ; J. Zhang ; J. A. Burmeister ; J. V. Califano ; J. P. Pandey ; H. A. Schenkein ; J. G. TewGenetic segregation analyses of serum IgG2 levels.
009C10 (1998) J A Becker ; J. Vlach ; N. Raben ; K. Nagaraju ; E M Adams ; M M Hermans ; A J Reuser ; S S Brooks ; C J Tifft ; R. Hirschhorn ; M L Huie ; M. Nicolino ; P H PlotzThe African origin of the common mutation in African American patients with glycogen-storage disease type II.
009C11 (1998) T J GillHLA and mate choice.
009C12 (1998) L. Kruglyak ; M J DalyLinkage thresholds for two-stage genome scans.
009C13 (1998) W. Ahmad ; V. Brancolini ; M F Ul Faiyaz ; H. Lam ; S. Ul Haque ; M. Haider ; A. Maimon ; V M Aita ; J. Owen ; D. Brown ; D J Zegarelli ; M. Ahmad ; J. Ott ; A M ChristianoA locus for autosomal recessive hypodontia with associated dental anomalies maps to chromosome 16q12.1.

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