-
1
-
-
0343726909
-
Osteo-dental dysplasia (cleido-cranialysostosis). The "Arnold head"
-
Jackson WPU. Osteo-dental dysplasia (cleido-cranialysostosis). The "Arnold head". Acta Med Scand 1951;139:292-307.
-
(1951)
Acta Med Scand
, vol.139
, pp. 292-307
-
-
Jackson, W.P.U.1
-
2
-
-
0026660151
-
Apparent cleidocranial dysplasia associated with abnormalities of 8q22 in three individuals
-
Brueton LA, Reeve A, Ellis R, Husband P, Thompson EM, Kingston HM. Apparent cleidocranial dysplasia associated with abnormalities of 8q22 in three individuals. Am J Med Genet 1992;43:612-18.
-
(1992)
Am J Med Genet
, vol.43
, pp. 612-618
-
-
Brueton, L.A.1
Reeve, A.2
Ellis, R.3
Husband, P.4
Thompson, E.M.5
Kingston, H.M.6
-
3
-
-
0027326695
-
Pericentric inversion of chromosome 6 in a patient with cleidocranial dysplasia
-
Nienhaus H, Mau U, Zang KD, Henn W. Pericentric inversion of chromosome 6 in a patient with cleidocranial dysplasia. Am J Med Genet 1993;46:630-1.
-
(1993)
Am J Med Genet
, vol.46
, pp. 630-631
-
-
Nienhaus, H.1
Mau, U.2
Zang, K.D.3
Henn, W.4
-
4
-
-
0028891018
-
Genetic mapping and evidence for a microdeletion in cleidocranial dysplasia
-
Mundlos S, Mulliken JB, Abramson DL, Warman ML, Knoll JHM, Olsen BR. Genetic mapping and evidence for a microdeletion in cleidocranial dysplasia. Hum Mol Genet 1995;4:71-5.
-
(1995)
Hum Mol Genet
, vol.4
, pp. 71-75
-
-
Mundlos, S.1
Mulliken, J.B.2
Abramson, D.L.3
Warman, M.L.4
Knoll, J.H.M.5
Olsen, B.R.6
-
5
-
-
0028928382
-
A gene for cleidocranial dysplasia maps to the short arm of chromosome 6
-
Feldman GJ, Robin NH, Brueton LA, et al. A gene for cleidocranial dysplasia maps to the short arm of chromosome 6. Am J Hum Genet 1995;56:938-43.
-
(1995)
Am J Hum Genet
, vol.56
, pp. 938-943
-
-
Feldman, G.J.1
Robin, N.H.2
Brueton, L.A.3
-
6
-
-
0029653567
-
Genetic mapping of cleidocranial dysplasia (CCD) locus on chromosome band 6p21 to include a microdeletion
-
Gelb BD, Cooper E, Shevell M, Desnick RJ. Genetic mapping of cleidocranial dysplasia (CCD) locus on chromosome band 6p21 to include a microdeletion. Am J Med Genet 1995;58:200-5.
-
(1995)
Am J Med Genet
, vol.58
, pp. 200-205
-
-
Gelb, B.D.1
Cooper, E.2
Shevell, M.3
Desnick, R.J.4
-
7
-
-
0028231090
-
The 1993-94 Genethon human genetic linkage map
-
Gyapay G, Morisette J, Vignal A, et al. The 1993-94 Genethon human genetic linkage map. Nature Genet 1994;7:246-92.
-
(1994)
Nature Genet
, vol.7
, pp. 246-292
-
-
Gyapay, G.1
Morisette, J.2
Vignal, A.3
-
8
-
-
0025886139
-
Linkage mapping and fluorescence in situ hybridisation of TCTE1 in human chromosome 6p: Analysis of dinucleotide polymorphisms on native gels
-
Kwiatkowski TJ Jr, Beaudet AL, Trask BJ, Zoghbi HY. Linkage mapping and fluorescence in situ hybridisation of TCTE1 in human chromosome 6p: analysis of dinucleotide polymorphisms on native gels. Genomics 1991;10:921-6.
-
(1991)
Genomics
, vol.10
, pp. 921-926
-
-
Kwiatkowski Jr., T.J.1
Beaudet, A.L.2
Trask, B.J.3
Zoghbi, H.Y.4
-
10
-
-
0021344005
-
Easy calculations of lod scores and genetic risks on small computers
-
Lathrop GM, Lalouel JM. Easy calculations of lod scores and genetic risks on small computers. Ant J Hum Genet 1984;36:460-5.
-
(1984)
Ant J Hum Genet
, vol.36
, pp. 460-465
-
-
Lathrop, G.M.1
Lalouel, J.M.2
-
11
-
-
0026564369
-
A bone morphogenetic protein subfamily: Chromosomal localisation of human genes for BMP5, BMP6, BMP7
-
Hahn GV, Cohen RB, Wozney JM, et al. A bone morphogenetic protein subfamily: chromosomal localisation of human genes for BMP5, BMP6, BMP7. Genomics 1992;14:759-62.
-
(1992)
Genomics
, vol.14
, pp. 759-762
-
-
Hahn, G.V.1
Cohen, R.B.2
Wozney, J.M.3
-
12
-
-
34250019537
-
Bone: Formation by autoinduction
-
Urist MR. Bone: formation by autoinduction. Science 1965;150:893-9.
-
(1965)
Science
, vol.150
, pp. 893-899
-
-
Urist, M.R.1
-
13
-
-
0026440993
-
The mouse short ear skeletal morphogenesis locus is associated with defects in a bone morphogenetic member of the TGF-beta superfamily
-
Kingsley DM, Bland AE, Grubber JM, et al. The mouse short ear skeletal morphogenesis locus is associated with defects in a bone morphogenetic member of the TGF-beta superfamily. Cell 1992;71:399-410.
-
(1992)
Cell
, vol.71
, pp. 399-410
-
-
Kingsley, D.M.1
Bland, A.E.2
Grubber, J.M.3
|