-
2
-
-
0023067846
-
Transmission of human craniofacial dimensions
-
E.J. Devor Transmission of human craniofacial dimensions J. Craniofac. Genet. Dev. Biol. 7 1987 95 106
-
(1987)
J. Craniofac. Genet. Dev. Biol.
, vol.7
, pp. 95-106
-
-
Devor, E.J.1
-
3
-
-
0022352103
-
Testing for the presence of genetic variance in factors of face measurements of Belgian twins
-
R.C. Hauspie, C. Susanne, and E. Defrise-Gussenhoven Testing for the presence of genetic variance in factors of face measurements of Belgian twins Ann. Hum. Biol. 12 1985 429 440
-
(1985)
Ann. Hum. Biol.
, vol.12
, pp. 429-440
-
-
Hauspie, R.C.1
Susanne, C.2
Defrise-Gussenhoven, E.3
-
4
-
-
0032431329
-
Sex differences in genetic determinants of craniofacial variations-a study based on twin kinships
-
K. Sharma Sex differences in genetic determinants of craniofacial variations-a study based on twin kinships Acta Genet. Med. Gemellol. (Rome) 47 1998 31 41
-
(1998)
Acta Genet. Med. Gemellol. (Rome)
, vol.47
, pp. 31-41
-
-
Sharma, K.1
-
5
-
-
0031922720
-
FGF-, BMP- and Shh-mediated signalling pathways in the regulation of cranial suture morphogenesis and calvarial bone development
-
H.J. Kim, D.P. Rice, P.J. Kettunen, and I. Thesleff FGF-, BMP- and Shh-mediated signalling pathways in the regulation of cranial suture morphogenesis and calvarial bone development Development 125 1998 1241 1251
-
(1998)
Development
, vol.125
, pp. 1241-1251
-
-
Kim, H.J.1
Rice, D.P.2
Kettunen, P.J.3
Thesleff, I.4
-
7
-
-
0028048771
-
Craniometric variation among modern human populations
-
J.H. Relethford Craniometric variation among modern human populations Am. J. Phys. Anthropol. 95 1994 53 62
-
(1994)
Am. J. Phys. Anthropol.
, vol.95
, pp. 53-62
-
-
Relethford, J.H.1
-
8
-
-
0027383692
-
Sutural biology and the correlates of craniosynostosis
-
M.M. Cohen Jr. Sutural biology and the correlates of craniosynostosis Am. J. Med. Genet. 47 1993 581 616
-
(1993)
Am. J. Med. Genet.
, vol.47
, pp. 581-616
-
-
Cohen Jr., M.M.1
-
9
-
-
0002825423
-
Craniosynostosis syndromes
-
C. Sciver A. Beaudet W. Sly D. Valle B. Childs B. Vogelstein McGraw-Hill New York
-
M. Muenke, and A.O. Wilkie Craniosynostosis syndromes C. Sciver A. Beaudet W. Sly D. Valle B. Childs B. Vogelstein The metabolic and molecular bases of inherited disease 2000 McGraw-Hill New York 6117 6146
-
(2000)
The Metabolic and Molecular Bases of Inherited Disease
, pp. 6117-6146
-
-
Muenke, M.1
Wilkie, A.O.2
-
10
-
-
0030769180
-
Craniosynostosis: Genes and mechanisms
-
A.O. Wilkie Craniosynostosis: genes and mechanisms Hum. Mol. Genet. 6 1997 1647 1656
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 1647-1656
-
-
Wilkie, A.O.1
-
11
-
-
0031021336
-
Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome
-
T.D. Howard Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome Nat. Genet. 15 1997 36 41
-
(1997)
Nat. Genet.
, vol.15
, pp. 36-41
-
-
Howard, T.D.1
-
12
-
-
0032774475
-
Clinical spectrum of fibroblast growth factor receptor mutations
-
M.R. Passos-Bueno Clinical spectrum of fibroblast growth factor receptor mutations Hum. Mutat. 14 1999 115 125
-
(1999)
Hum. Mutat.
, vol.14
, pp. 115-125
-
-
Passos-Bueno, M.R.1
-
13
-
-
0034601248
-
Clinical findings in a patient with FGFR1 P252R mutation and comparison with the literature
-
T. Roscioli Clinical findings in a patient with FGFR1 P252R mutation and comparison with the literature Am. J. Med. Genet. 93 2000 22 28
-
(2000)
Am. J. Med. Genet.
, vol.93
, pp. 22-28
-
-
Roscioli, T.1
-
14
-
-
0029109137
-
Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes
-
P. Rutl Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes Nat. Genet. 9 1995 173 176
-
(1995)
Nat. Genet.
, vol.9
, pp. 173-176
-
-
Rutl, P.1
-
15
-
-
0036821229
-
Expression profiles of craniosynostosis-derived fibroblasts
-
F. Carinci Expression profiles of craniosynostosis-derived fibroblasts Mol. Med. 8 2002 638 644
-
(2002)
Mol. Med.
, vol.8
, pp. 638-644
-
-
Carinci, F.1
-
16
-
-
16244399678
-
Kallmann syndrome: 14 novel mutations in KAL1 and FGFR1 (KAL2)
-
J. Albuisson Kallmann syndrome: 14 novel mutations in KAL1 and FGFR1 (KAL2) Hum. Mutat. 25 2005 98 99
-
(2005)
Hum. Mutat.
, vol.25
, pp. 98-99
-
-
Albuisson, J.1
-
17
-
-
0036362757
-
The structure and function of vertebrate fibroblast growth factor receptor 1
-
C. Groth, and M. Lardelli The structure and function of vertebrate fibroblast growth factor receptor 1 Int. J. Dev. Biol. 46 2002 393 400
-
(2002)
Int. J. Dev. Biol.
, vol.46
, pp. 393-400
-
-
Groth, C.1
Lardelli, M.2
-
18
-
-
0038499403
-
Craniofacial development: The tissue and molecular interactions that control development of the head
-
P.H. Francis-West, L. Robson, and D.J. Evans Craniofacial development: the tissue and molecular interactions that control development of the head Adv. Anat. Embryol. Cell Biol. 169 III-VI 2003 1 138
-
(2003)
Adv. Anat. Embryol. Cell Biol.
, vol.169
, Issue.3-6
, pp. 1-138
-
-
Francis-West, P.H.1
Robson, L.2
Evans, D.J.3
-
19
-
-
0034914581
-
Canine TCOF1; Cloning, chromosome assignment and genetic analysis in dogs with different head types
-
K.E. Haworth Canine TCOF1; cloning, chromosome assignment and genetic analysis in dogs with different head types Mamm. Genome 12 2001 622 629
-
(2001)
Mamm. Genome
, vol.12
, pp. 622-629
-
-
Haworth, K.E.1
-
20
-
-
0031012353
-
Mutations of the TWIST gene in the Saethre-Chotzen syndrome
-
V. El Ghouzzi Mutations of the TWIST gene in the Saethre-Chotzen syndrome Nat. Genet. 15 1997 42 46
-
(1997)
Nat. Genet.
, vol.15
, pp. 42-46
-
-
El Ghouzzi, V.1
-
21
-
-
0032231374
-
A comprehensive screen for TWIST mutations in patients with craniosynostosis identifies a new microdeletion syndrome of chromosome band 7p21.1
-
D. Johnson A comprehensive screen for TWIST mutations in patients with craniosynostosis identifies a new microdeletion syndrome of chromosome band 7p21.1 Am. J. Hum. Genet. 63 1998 1282 1293
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 1282-1293
-
-
Johnson, D.1
-
22
-
-
0034320115
-
Identification of a polymorphism (G83S) in the TWIST gene in Taiwanese
-
C.F. Yang, J.Y. Wu, F.J. Tsai, C.C. Lee, and W.D. Lin Identification of a polymorphism (G83S) in the TWIST gene in Taiwanese Hum. Mutat. 16 2000 448
-
(2000)
Hum. Mutat.
, vol.16
, pp. 448
-
-
Yang, C.F.1
Wu, J.Y.2
Tsai, F.J.3
Lee, C.C.4
Lin, W.D.5
-
23
-
-
0006973251
-
Molecular analysis of patients with Saethre-Chotzen syndrome: Novel mutations and polymorphisms in the TWIST gene
-
V. Kasparcova Molecular analysis of patients with Saethre-Chotzen syndrome: novel mutations and polymorphisms in the TWIST gene Am. J. Hum. Genet. 63 1998 abs 2126 Suppl.
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 2126
-
-
Kasparcova, V.1
-
24
-
-
0028046606
-
A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome
-
M. Muenke A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome Nat. Genet. 8 1994 269 274
-
(1994)
Nat. Genet.
, vol.8
, pp. 269-274
-
-
Muenke, M.1
-
25
-
-
12144288744
-
Clinical assessment and mutation analysis of Kallmann syndrome 1 (KAL1) and fibroblast growth factor receptor 1 (FGFR1, or KAL2) in five families and 18 sporadic patients
-
N. Sato Clinical assessment and mutation analysis of Kallmann syndrome 1 (KAL1) and fibroblast growth factor receptor 1 (FGFR1, or KAL2) in five families and 18 sporadic patients J. Clin. Endocrinol. Metab. 89 2004 1079 1088
-
(2004)
J. Clin. Endocrinol. Metab.
, vol.89
, pp. 1079-1088
-
-
Sato, N.1
-
26
-
-
20244366799
-
Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome
-
C. Dode Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome Nat. Genet. 33 2003 463 465
-
(2003)
Nat. Genet.
, vol.33
, pp. 463-465
-
-
Dode, C.1
-
27
-
-
0035972812
-
Two distal Sp1-binding cis-elements regulate fibroblast growth factor receptor 1 (FGFR1) gene expression in myoblasts
-
S.G. Patel, and J.X. DiMario Two distal Sp1-binding cis-elements regulate fibroblast growth factor receptor 1 (FGFR1) gene expression in myoblasts Gene 270 2001 171 180
-
(2001)
Gene
, vol.270
, pp. 171-180
-
-
Patel, S.G.1
Dimario, J.X.2
-
28
-
-
0037088692
-
Sp1- and Sp3-mediated transcriptional regulation of the fibroblast growth factor receptor 1 gene in chicken skeletal muscle cells
-
R. Parakati, and J.X. DiMario Sp1- and Sp3-mediated transcriptional regulation of the fibroblast growth factor receptor 1 gene in chicken skeletal muscle cells J. Biol. Chem. 277 2002 9278 9285
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 9278-9285
-
-
Parakati, R.1
Dimario, J.X.2
-
29
-
-
0033992637
-
Gene mapping in isolated populations: New roles for old friends?
-
L.B. Jorde, W.S. Watkins, J. Kere, D. Nyman, and A.W. Eriksson Gene mapping in isolated populations: new roles for old friends? Hum. Hered. 50 2000 57 65
-
(2000)
Hum. Hered.
, vol.50
, pp. 57-65
-
-
Jorde, L.B.1
Watkins, W.S.2
Kere, J.3
Nyman, D.4
Eriksson, A.W.5
-
30
-
-
18444369013
-
The structure of haplotype blocks in the human genome
-
S.B. Gabriel The structure of haplotype blocks in the human genome Science 296 2002 2225 2229
-
(2002)
Science
, vol.296
, pp. 2225-2229
-
-
Gabriel, S.B.1
-
31
-
-
0000622405
-
Genetic differences within and between populations of the major human subgroups
-
B. Latter Genetic differences within and between populations of the major human subgroups Am. Nat. 116 1980 220 237
-
(1980)
Am. Nat.
, vol.116
, pp. 220-237
-
-
Latter, B.1
-
32
-
-
0000244010
-
The apportionment of human diversity
-
R.C. Lewontin The apportionment of human diversity Evol. Biol. 6 1972 381 398
-
(1972)
Evol. Biol.
, vol.6
, pp. 381-398
-
-
Lewontin, R.C.1
-
33
-
-
0033912515
-
The distribution of human genetic diversity: A comparison of mitochondrial, autosomal, and Y-chromosome data
-
L.B. Jorde The distribution of human genetic diversity: a comparison of mitochondrial, autosomal, and Y-chromosome data Am. J. Hum. Genet. 66 2000 979 988
-
(2000)
Am. J. Hum. Genet.
, vol.66
, pp. 979-988
-
-
Jorde, L.B.1
-
34
-
-
0036226789
-
Patterns of human diversity, within and among continents, inferred from biallelic DNA polymorphisms
-
C. Romualdi Patterns of human diversity, within and among continents, inferred from biallelic DNA polymorphisms Genome Res. 12 2002 602 612
-
(2002)
Genome Res.
, vol.12
, pp. 602-612
-
-
Romualdi, C.1
-
35
-
-
0036136606
-
Geometric morphometric study of the regional variation of modern human craniofacial form
-
R.J. Hennessy, and C.B. Stringer Geometric morphometric study of the regional variation of modern human craniofacial form Am. J. Phys. Anthropol. 117 2002 37 48
-
(2002)
Am. J. Phys. Anthropol.
, vol.117
, pp. 37-48
-
-
Hennessy, R.J.1
Stringer, C.B.2
-
36
-
-
0036329295
-
Apportionment of global human genetic diversity based on craniometrics and skin color
-
J.H. Relethford Apportionment of global human genetic diversity based on craniometrics and skin color Am. J. Phys. Anthropol. 118 2002 393 398
-
(2002)
Am. J. Phys. Anthropol.
, vol.118
, pp. 393-398
-
-
Relethford, J.H.1
-
37
-
-
0038813684
-
Genomics: Not junk after all
-
W. Makalowski Genomics: not junk after all Science 300 2003 1246 1247
-
(2003)
Science
, vol.300
, pp. 1246-1247
-
-
Makalowski, W.1
-
38
-
-
0037504164
-
Molecular biology: Spinning junk into gold
-
I. Wickelgren Molecular biology: spinning junk into gold Science 300 2003 1646 1649
-
(2003)
Science
, vol.300
, pp. 1646-1649
-
-
Wickelgren, I.1
-
41
-
-
0035071957
-
A new statistical method for haplotype reconstruction from population data
-
M. Stephens, N.J. Smith, and P. Donnelly A new statistical method for haplotype reconstruction from population data Am. J. Hum. Genet. 68 2001 978 989
-
(2001)
Am. J. Hum. Genet.
, vol.68
, pp. 978-989
-
-
Stephens, M.1
Smith, N.J.2
Donnelly, P.3
-
42
-
-
0242691208
-
A comparison of Bayesian methods for haplotype reconstruction from population genotype data
-
M. Stephens, and P. Donnelly A comparison of Bayesian methods for haplotype reconstruction from population genotype data Am. J. Hum. Genet. 73 2003 1162 1169
-
(2003)
Am. J. Hum. Genet.
, vol.73
, pp. 1162-1169
-
-
Stephens, M.1
Donnelly, P.2
-
43
-
-
0034017850
-
GOLD-graphical overview of linkage disequilibrium
-
G.R. Abecasis, and W.O. Cookson GOLD-graphical overview of linkage disequilibrium Bioinformatics 16 2000 182 183
-
(2000)
Bioinformatics
, vol.16
, pp. 182-183
-
-
Abecasis, G.R.1
Cookson, W.O.2
-
44
-
-
0003752712
-
-
Sinauer, Sunderland, MA.
-
B. Weir, (1996). Genetic Data Analysis II, Sinauer, http://linkage. rockefeller.edu/ott/linkutil.htm, Sunderland, MA.
-
(1996)
Genetic Data Analysis II
-
-
Weir, B.1
-
45
-
-
30344478140
-
-
WAIMR, Perth, Western Australia.
-
K. Carter, P. McCaskie, L. Palmer (2004). Java Linkage Disequilibrium Plotter, WAIMR, http://www.genepi.com.au/projects/jlin/, Perth, Western Australia.
-
(2004)
Java Linkage Disequilibrium Plotter
-
-
Carter, K.1
McCaskie, P.2
Palmer, L.3
-
46
-
-
0003402305
-
-
Genetics and Biometry Laboratory, Department of Anthropology, University of Geneva, Geneva.
-
S. Schneider, D. Roessli, L. Excoffier (2000). Arlequin version 2.000: software for population genetics data analysis, Genetics and Biometry Laboratory, Department of Anthropology, University of Geneva, http://lgb.unige.ch/arlequin/, Geneva.
-
(2000)
Arlequin Version 2.000: Software for Population Genetics Data Analysis
-
-
Schneider, S.1
Roessli, D.2
Excoffier, L.3
|