0002-9270 < 0002-9297 < 0002-9343

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List of bibliographic references indexed by 0002-9297

Number of relevant bibliographic references: 15.

Ident.	Authors (with country if any)	Title
008317 (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
009046 (2000)	Vandana Shashi [États-Unis] ; Margaret N. Berry [États-Unis] ; Sarah Shoaf [États-Unis] ; James J. Sciote [États-Unis] ; Donald Goldstein [États-Unis] ; Thomas C. Hart [États-Unis]	A Unique Form of Mental Retardation with a Distinctive Phenotype Maps to Xq26-q27
009664 (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 Plotz	The African origin of the common mutation in African American patients with glycogen-storage disease type II.
009714 (1998)	L. Kruglyak ; M J Daly	Linkage thresholds for two-stage genome scans.
009727 (1998)	T J Gill	HLA and mate choice.
009785 (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 Christiano	A locus for autosomal recessive hypodontia with associated dental anomalies maps to chromosome 16q12.1.
00A065 (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. Tew	Genetic segregation analyses of serum IgG2 levels.
00AD67 (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 Breuning	Deletion at chromosome 16p13.3 as a cause of Rubinstein-Taybi syndrome: clinical aspects.
00B115 (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. Thomas	High-resolution mapping of the X-linked hypohidrotic ectodermal dysplasia (EDA) locus
00B810 (1990)	M. Lagerström ; N. Dahl ; L. Iselius ; B. B Ckman ; U. Pettersson	Mapping of the gene for X-linked amelogenesis imperfecta by linkage analysis.
00BE47 (1988)	J. Zonana ; A. Clarke ; M. Sarfarazi ; N S Thomas ; K. Roberts ; K. Marymee ; P S Harper	X-linked hypohidrotic ectodermal dysplasia: localization within the region Xq11-21.1 by linkage analysis and implications for carrier detection and prenatal diagnosis.
00C306 (1987)	T H Beaty ; J A Boughman ; P. Yang ; J A Astemborski ; J B Suzuki	Genetic analysis of juvenile periodontitis in families ascertained through an affected proband.
00E609 (1972)	J. Lichtenstein ; R. Warson ; R. Jorgenson ; J P Dorst ; V A Mckusick	The tricho-dento-osseous (TDO) syndrome.
00E626 (1972)	J C Gall ; A M Stern ; A K Poznanski ; S M Garn ; E D Weinstein ; J R Hayward	Oto-palato-digital syndrome: comparison of clinical and radiographic manifestations in males and females.
00F086 (1962)	Eldon J. Gardner	Follow-up Study of a Family Group Exhibiting Dominant Inheritance for a Syndrome Including Intestinal Polyps, Osteomas, Fibromas and Epidermal Cysts

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