-
1
-
-
78650206677
-
Updated National Birth Prevalence estimates for selected birth defects in the United States, 2004-2006
-
Parker SE, Mai CT, Canfield MA, Rickard R, Wang Y, et al. (2010) Updated National Birth Prevalence estimates for selected birth defects in the United States, 2004-2006. Birth Defects Res A Clin Mol Teratol 88: 1008-1016.
-
(2010)
Birth Defects Res A Clin Mol Teratol
, vol.88
, pp. 1008-1016
-
-
Parker, S.E.1
Mai, C.T.2
Canfield, M.A.3
Rickard, R.4
Wang, Y.5
-
2
-
-
38849143911
-
Population-based birth defects surveillance data from selected states, 2000-2004
-
Population-based birth defects surveillance data from selected states, 2000-2004. Birth Defects Res A Clin Mol Teratol 79: 874-942.
-
Birth Defects Res A Clin Mol Teratol
, vol.79
, pp. 874-942
-
-
-
3
-
-
65649144240
-
Recognition of caudal regression syndrome
-
Boulas MM, (2009) Recognition of caudal regression syndrome. Adv Neonatal Care 9: 61-69 quiz 70-61.
-
(2009)
Adv Neonatal Care
, vol.9
, pp. 61-69
-
-
Boulas, M.M.1
-
4
-
-
0032751788
-
Polytopic anomalies with agenesis of the lower vertebral column
-
Bohring A, Lewin SO, Reynolds JF, Voigtlander T, Rittinger O, et al. (1999) Polytopic anomalies with agenesis of the lower vertebral column. Am J Med Genet 87: 99-114.
-
(1999)
Am J Med Genet
, vol.87
, pp. 99-114
-
-
Bohring, A.1
Lewin, S.O.2
Reynolds, J.F.3
Voigtlander, T.4
Rittinger, O.5
-
5
-
-
17344363829
-
A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis
-
Ross AJ, Ruiz-Perez V, Wang Y, Hagan DM, Scherer S, et al. (1998) A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis. Nat Genet 20: 358-361.
-
(1998)
Nat Genet
, vol.20
, pp. 358-361
-
-
Ross, A.J.1
Ruiz-Perez, V.2
Wang, Y.3
Hagan, D.M.4
Scherer, S.5
-
6
-
-
1642327710
-
Evolving concepts in human renal dysplasia
-
Woolf AS, Price KL, Scambler PJ, Winyard PJ, (2004) Evolving concepts in human renal dysplasia. J Am Soc Nephrol 15: 998-1007.
-
(2004)
J Am Soc Nephrol
, vol.15
, pp. 998-1007
-
-
Woolf, A.S.1
Price, K.L.2
Scambler, P.J.3
Winyard, P.J.4
-
7
-
-
34548787844
-
Renal abnormalities and their developmental origin
-
Schedl A, (2007) Renal abnormalities and their developmental origin. Nat Rev Genet 8: 791-802.
-
(2007)
Nat Rev Genet
, vol.8
, pp. 791-802
-
-
Schedl, A.1
-
8
-
-
33749241883
-
Prevalence of mutations in renal developmental genes in children with renal hypodysplasia: results of the ESCAPE study
-
Weber S, Moriniere V, Knuppel T, Charbit M, Dusek J, et al. (2006) Prevalence of mutations in renal developmental genes in children with renal hypodysplasia: results of the ESCAPE study. J Am Soc Nephrol 17: 2864-2870.
-
(2006)
J Am Soc Nephrol
, vol.17
, pp. 2864-2870
-
-
Weber, S.1
Moriniere, V.2
Knuppel, T.3
Charbit, M.4
Dusek, J.5
-
9
-
-
33645454942
-
Renal phenotypes related to hepatocyte nuclear factor-1beta (TCF2) mutations in a pediatric cohort
-
Ulinski T, Lescure S, Beaufils S, Guigonis V, Decramer S, et al. (2006) Renal phenotypes related to hepatocyte nuclear factor-1beta (TCF2) mutations in a pediatric cohort. J Am Soc Nephrol 17: 497-503.
-
(2006)
J Am Soc Nephrol
, vol.17
, pp. 497-503
-
-
Ulinski, T.1
Lescure, S.2
Beaufils, S.3
Guigonis, V.4
Decramer, S.5
-
10
-
-
79959953210
-
HNF1B and PAX2 mutations are a common cause of renal hypodysplasia in the CKiD cohort
-
Thomas R, Sanna-Cherchi S, Warady BA, Furth SL, Kaskel FJ, et al. (2011) HNF1B and PAX2 mutations are a common cause of renal hypodysplasia in the CKiD cohort. Pediatr Nephrol 26: 897-903.
-
(2011)
Pediatr Nephrol
, vol.26
, pp. 897-903
-
-
Thomas, R.1
Sanna-Cherchi, S.2
Warady, B.A.3
Furth, S.L.4
Kaskel, F.J.5
-
11
-
-
0004330255
-
Developmental Anomalies in a Special Strain of Mice
-
Danforth CH, (1930) Developmental Anomalies in a Special Strain of Mice. Amer Jour Anat 45: 275-287.
-
(1930)
Amer Jour Anat
, vol.45
, pp. 275-287
-
-
Danforth, C.H.1
-
12
-
-
0000496537
-
A New Mutation in the Mouse: Affecting Spinal Column and Urogenital System J Heredity
-
Dunn LC, Gluecksohn-Schoenheimer S, Bryson V, (1940) A New Mutation in the Mouse: Affecting Spinal Column and Urogenital System J Heredity. 31: 343-348.
-
(1940)
, vol.31
, pp. 343-348
-
-
Dunn, L.C.1
Gluecksohn-Schoenheimer, S.2
Bryson, V.3
-
13
-
-
0006740941
-
The Morphological Manifestations of a Dominant Mutation in Mice Affecting Tail and Urogenital System
-
Gluecksohn-Schoenheimer S, (1943) The Morphological Manifestations of a Dominant Mutation in Mice Affecting Tail and Urogenital System. Genetics 28: 341-348.
-
(1943)
Genetics
, vol.28
, pp. 341-348
-
-
Gluecksohn-Schoenheimer, S.1
-
14
-
-
0040548750
-
The Embryonic Development of Mutants of the Sd-Strain in Mice
-
Gluecksohn-Schoenheimer S, (1945) The Embryonic Development of Mutants of the Sd-Strain in Mice. Genetics 30: 29-38.
-
(1945)
Genetics
, vol.30
, pp. 29-38
-
-
Gluecksohn-Schoenheimer, S.1
-
15
-
-
0043154950
-
Genetical studies on the skeleton of the mouse. XXII. The development of Danforth's short-tail
-
Gruneberg H, (1958) Genetical studies on the skeleton of the mouse. XXII. The development of Danforth's short-tail. J Embryol Exp Morphol 6: 124-148.
-
(1958)
J Embryol Exp Morphol
, vol.6
, pp. 124-148
-
-
Gruneberg, H.1
-
16
-
-
0032533318
-
Apoptosis of epaxial myotome in Danforth's short-tail (Sd) mice in somites that form following notochord degeneration
-
Asakura A, Tapscott SJ, (1998) Apoptosis of epaxial myotome in Danforth's short-tail (Sd) mice in somites that form following notochord degeneration. Dev Biol 203: 276-289.
-
(1998)
Dev Biol
, vol.203
, pp. 276-289
-
-
Asakura, A.1
Tapscott, S.J.2
-
17
-
-
0030817265
-
The Danforth's short tail mutation acts cell autonomously in notochord cells and ventral hindgut endoderm
-
Maatman R, Zachgo J, Gossler A, (1997) The Danforth's short tail mutation acts cell autonomously in notochord cells and ventral hindgut endoderm. Development 124: 4019-4028.
-
(1997)
Development
, vol.124
, pp. 4019-4028
-
-
Maatman, R.1
Zachgo, J.2
Gossler, A.3
-
18
-
-
77951206973
-
Midline signaling regulates kidney positioning but not nephrogenesis through Shh
-
Tripathi P, Guo Q, Wang Y, Coussens M, Liapis H, et al. (2010) Midline signaling regulates kidney positioning but not nephrogenesis through Shh. Dev Biol 340: 518-527.
-
(2010)
Dev Biol
, vol.340
, pp. 518-527
-
-
Tripathi, P.1
Guo, Q.2
Wang, Y.3
Coussens, M.4
Liapis, H.5
-
19
-
-
0030894414
-
Mapping in the region of Danforth's short tail and the localization of tail length modifiers
-
Alfred JB, Rance K, Taylor BA, Phillips SJ, Abbott CM, et al. (1997) Mapping in the region of Danforth's short tail and the localization of tail length modifiers. Genome Res 7: 108-117.
-
(1997)
Genome Res
, vol.7
, pp. 108-117
-
-
Alfred, J.B.1
Rance, K.2
Taylor, B.A.3
Phillips, S.J.4
Abbott, C.M.5
-
20
-
-
33645757337
-
Retroviral elements and their hosts: insertional mutagenesis in the mouse germ line
-
doi: 10.1371/journal.pgen.0020002
-
Maksakova IA, Romanish MT, Gagnier L, Dunn CA, van de Lagemaat LN, et al. (2006) Retroviral elements and their hosts: insertional mutagenesis in the mouse germ line. PLoS Genet 2: e2 doi:10.1371/journal.pgen.0020002.
-
(2006)
PLoS Genet
, vol.2
-
-
Maksakova, I.A.1
Romanish, M.T.2
Gagnier, L.3
Dunn, C.A.4
van de Lagemaat, L.N.5
-
21
-
-
84862203271
-
The genomic landscape shaped by selection on transposable elements across 18 mouse strains
-
Nellaker C, Keane TM, Yalcin B, Wong K, Agam A, et al. (2012) The genomic landscape shaped by selection on transposable elements across 18 mouse strains. Genome Biol 13: R45.
-
(2012)
Genome Biol
, vol.13
-
-
Nellaker, C.1
Keane, T.M.2
Yalcin, B.3
Wong, K.4
Agam, A.5
-
22
-
-
0037040583
-
Purkinje cell degeneration (pcd) phenotypes caused by mutations in the axotomy-induced gene, Nna1
-
Fernandez-Gonzalez A, La Spada AR, Treadaway J, Higdon JC, Harris BS, et al. (2002) Purkinje cell degeneration (pcd) phenotypes caused by mutations in the axotomy-induced gene, Nna1. Science 295: 1904-1906.
-
(2002)
Science
, vol.295
, pp. 1904-1906
-
-
Fernandez-Gonzalez, A.1
La Spada, A.R.2
Treadaway, J.3
Higdon, J.C.4
Harris, B.S.5
-
23
-
-
0029094912
-
Retinal degeneration slow (rds) in mouse results from simple insertion of a t haplotype-specific element into protein-coding exon II
-
Ma J, Norton JC, Allen AC, Burns JB, Hasel KW, et al. (1995) Retinal degeneration slow (rds) in mouse results from simple insertion of a t haplotype-specific element into protein-coding exon II. Genomics 28: 212-219.
-
(1995)
Genomics
, vol.28
, pp. 212-219
-
-
Ma, J.1
Norton, J.C.2
Allen, A.C.3
Burns, J.B.4
Hasel, K.W.5
-
24
-
-
58549093915
-
Developmental biology of the pancreas: a comprehensive review
-
Gittes GK, (2009) Developmental biology of the pancreas: a comprehensive review. Dev Biol 326: 4-35.
-
(2009)
Dev Biol
, vol.326
, pp. 4-35
-
-
Gittes, G.K.1
-
25
-
-
50249106419
-
Transcriptional autoregulation controls pancreatic Ptf1a expression during development and adulthood
-
Masui T, Swift GH, Hale MA, Meredith DM, Johnson JE, et al. (2008) Transcriptional autoregulation controls pancreatic Ptf1a expression during development and adulthood. Mol Cell Biol 28: 5458-5468.
-
(2008)
Mol Cell Biol
, vol.28
, pp. 5458-5468
-
-
Masui, T.1
Swift, G.H.2
Hale, M.A.3
Meredith, D.M.4
Johnson, J.E.5
-
26
-
-
70349094112
-
Multiple transcriptional mechanisms control Ptf1a levels during neural development including autoregulation by the PTF1-J complex
-
Meredith DM, Masui T, Swift GH, MacDonald RJ, Johnson JE, (2009) Multiple transcriptional mechanisms control Ptf1a levels during neural development including autoregulation by the PTF1-J complex. J Neurosci 29: 11139-11148.
-
(2009)
J Neurosci
, vol.29
, pp. 11139-11148
-
-
Meredith, D.M.1
Masui, T.2
Swift, G.H.3
MacDonald, R.J.4
Johnson, J.E.5
-
27
-
-
0035046997
-
p48 subunit of mouse PTF1 binds to RBP-Jkappa/CBF-1, the intracellular mediator of Notch signalling, and is expressed in the neural tube of early stage embryos
-
Obata J, Yano M, Mimura H, Goto T, Nakayama R, et al. (2001) p48 subunit of mouse PTF1 binds to RBP-Jkappa/CBF-1, the intracellular mediator of Notch signalling, and is expressed in the neural tube of early stage embryos. Genes to cells: devoted to molecular & cellular mechanisms 6: 345-360.
-
(2001)
Genes to Cells: Devoted to Molecular & Cellular Mechanisms
, vol.6
, pp. 345-360
-
-
Obata, J.1
Yano, M.2
Mimura, H.3
Goto, T.4
Nakayama, R.5
-
28
-
-
0036730427
-
The role of the transcriptional regulator Ptf1a in converting intestinal to pancreatic progenitors
-
Kawaguchi Y, Cooper B, Gannon M, Ray M, MacDonald RJ, et al. (2002) The role of the transcriptional regulator Ptf1a in converting intestinal to pancreatic progenitors. Nature genetics 32: 128-134.
-
(2002)
Nature Genetics
, vol.32
, pp. 128-134
-
-
Kawaguchi, Y.1
Cooper, B.2
Gannon, M.3
Ray, M.4
MacDonald, R.J.5
-
29
-
-
84857846185
-
RNA profiling and chromatin immunoprecipitation-sequencing reveal that PTF1a stabilizes pancreas progenitor identity via the control of MNX1/HLXB9 and a network of other transcription factors
-
Thompson N, Gesina E, Scheinert P, Bucher P, Grapin-Botton A, (2012) RNA profiling and chromatin immunoprecipitation-sequencing reveal that PTF1a stabilizes pancreas progenitor identity via the control of MNX1/HLXB9 and a network of other transcription factors. Molecular and cellular biology 32: 1189-1199.
-
(2012)
Molecular and Cellular Biology
, vol.32
, pp. 1189-1199
-
-
Thompson, N.1
Gesina, E.2
Scheinert, P.3
Bucher, P.4
Grapin-Botton, A.5
-
30
-
-
69049083510
-
Neurog2 is a direct downstream target of the Ptf1a-Rbpj transcription complex in dorsal spinal cord
-
Henke RM, Savage TK, Meredith DM, Glasgow SM, Hori K, et al. (2009) Neurog2 is a direct downstream target of the Ptf1a-Rbpj transcription complex in dorsal spinal cord. Development 136: 2945-2954.
-
(2009)
Development
, vol.136
, pp. 2945-2954
-
-
Henke, R.M.1
Savage, T.K.2
Meredith, D.M.3
Glasgow, S.M.4
Hori, K.5
-
31
-
-
38349060863
-
A nonclassical bHLH Rbpj transcription factor complex is required for specification of GABAergic neurons independent of Notch signaling
-
Hori K, Cholewa-Waclaw J, Nakada Y, Glasgow SM, Masui T, et al. (2008) A nonclassical bHLH Rbpj transcription factor complex is required for specification of GABAergic neurons independent of Notch signaling. Genes Dev 22: 166-178.
-
(2008)
Genes Dev
, vol.22
, pp. 166-178
-
-
Hori, K.1
Cholewa-Waclaw, J.2
Nakada, Y.3
Glasgow, S.M.4
Masui, T.5
-
32
-
-
29144516650
-
Ptf1a determines GABAergic over glutamatergic neuronal cell fate in the spinal cord dorsal horn
-
Glasgow SM, Henke RM, Macdonald RJ, Wright CV, Johnson JE, (2005) Ptf1a determines GABAergic over glutamatergic neuronal cell fate in the spinal cord dorsal horn. Development 132: 5461-5469.
-
(2005)
Development
, vol.132
, pp. 5461-5469
-
-
Glasgow, S.M.1
Henke, R.M.2
Macdonald, R.J.3
Wright, C.V.4
Johnson, J.E.5
-
33
-
-
0035046997
-
p48 subunit of mouse PTF1 binds to RBP-Jkappa/CBF-1, the intracellular mediator of Notch signalling, and is expressed in the neural tube of early stage embryos
-
Obata J, Yano M, Mimura H, Goto T, Nakayama R, et al. (2001) p48 subunit of mouse PTF1 binds to RBP-Jkappa/CBF-1, the intracellular mediator of Notch signalling, and is expressed in the neural tube of early stage embryos. Genes Cells 6: 345-360.
-
(2001)
Genes Cells
, vol.6
, pp. 345-360
-
-
Obata, J.1
Yano, M.2
Mimura, H.3
Goto, T.4
Nakayama, R.5
-
34
-
-
0024746213
-
The cell-specific transcription factor PTF1 contains two different subunits that interact with the DNA
-
Roux E, Strubin M, Hagenbuchle O, Wellauer PK, (1989) The cell-specific transcription factor PTF1 contains two different subunits that interact with the DNA. Genes Dev 3: 1613-1624.
-
(1989)
Genes Dev
, vol.3
, pp. 1613-1624
-
-
Roux, E.1
Strubin, M.2
Hagenbuchle, O.3
Wellauer, P.K.4
-
35
-
-
0036730427
-
The role of the transcriptional regulator Ptf1a in converting intestinal to pancreatic progenitors
-
Kawaguchi Y, Cooper B, Gannon M, Ray M, MacDonald RJ, et al. (2002) The role of the transcriptional regulator Ptf1a in converting intestinal to pancreatic progenitors. Nat Genet 32: 128-134.
-
(2002)
Nat Genet
, vol.32
, pp. 128-134
-
-
Kawaguchi, Y.1
Cooper, B.2
Gannon, M.3
Ray, M.4
MacDonald, R.J.5
-
36
-
-
35348985382
-
Early pancreatic development requires the vertebrate Suppressor of Hairless (RBPJ) in the PTF1 bHLH complex
-
Masui T, Long Q, Beres TM, Magnuson MA, MacDonald RJ, (2007) Early pancreatic development requires the vertebrate Suppressor of Hairless (RBPJ) in the PTF1 bHLH complex. Genes Dev 21: 2629-2643.
-
(2007)
Genes Dev
, vol.21
, pp. 2629-2643
-
-
Masui, T.1
Long, Q.2
Beres, T.M.3
Magnuson, M.A.4
MacDonald, R.J.5
-
37
-
-
33645236232
-
PTF1 is an organ-specific and Notch-independent basic helix-loop-helix complex containing the mammalian Suppressor of Hairless (RBP-J) or its paralogue, RBP-L
-
Beres TM, Masui T, Swift GH, Shi L, Henke RM, et al. (2006) PTF1 is an organ-specific and Notch-independent basic helix-loop-helix complex containing the mammalian Suppressor of Hairless (RBP-J) or its paralogue, RBP-L. Mol Cell Biol 26: 117-130.
-
(2006)
Mol Cell Biol
, vol.26
, pp. 117-130
-
-
Beres, T.M.1
Masui, T.2
Swift, G.H.3
Shi, L.4
Henke, R.M.5
-
38
-
-
33845897880
-
Ptf1a determines horizontal and amacrine cell fates during mouse retinal development
-
Fujitani Y, Fujitani S, Luo H, Qiu F, Burlison J, et al. (2006) Ptf1a determines horizontal and amacrine cell fates during mouse retinal development. Development 133: 4439-4450.
-
(2006)
Development
, vol.133
, pp. 4439-4450
-
-
Fujitani, Y.1
Fujitani, S.2
Luo, H.3
Qiu, F.4
Burlison, J.5
-
39
-
-
9644255692
-
Mutations in PTF1A cause pancreatic and cerebellar agenesis
-
Sellick GS, Barker KT, Stolte-Dijkstra I, Fleischmann C, Coleman RJ, et al. (2004) Mutations in PTF1A cause pancreatic and cerebellar agenesis. Nat Genet 36: 1301-1305.
-
(2004)
Nat Genet
, vol.36
, pp. 1301-1305
-
-
Sellick, G.S.1
Barker, K.T.2
Stolte-Dijkstra, I.3
Fleischmann, C.4
Coleman, R.J.5
-
40
-
-
33745684608
-
Ascl1 and Gsh1/2 control inhibitory and excitatory cell fate in spinal sensory interneurons
-
Mizuguchi R, Kriks S, Cordes R, Gossler A, Ma Q, et al. (2006) Ascl1 and Gsh1/2 control inhibitory and excitatory cell fate in spinal sensory interneurons. Nat Neurosci 9: 770-778.
-
(2006)
Nat Neurosci
, vol.9
, pp. 770-778
-
-
Mizuguchi, R.1
Kriks, S.2
Cordes, R.3
Gossler, A.4
Ma, Q.5
-
41
-
-
22544464692
-
Ptf1a, a bHLH transcriptional gene, defines GABAergic neuronal fates in cerebellum
-
Hoshino M, Nakamura S, Mori K, Kawauchi T, Terao M, et al. (2005) Ptf1a, a bHLH transcriptional gene, defines GABAergic neuronal fates in cerebellum. Neuron 47: 201-213.
-
(2005)
Neuron
, vol.47
, pp. 201-213
-
-
Hoshino, M.1
Nakamura, S.2
Mori, K.3
Kawauchi, T.4
Terao, M.5
-
42
-
-
34247644810
-
Cerebellar GABAergic progenitors adopt an external granule cell-like phenotype in the absence of Ptf1a transcription factor expression
-
Pascual M, Abasolo I, Mingorance-Le Meur A, Martinez A, Del Rio JA, et al. (2007) Cerebellar GABAergic progenitors adopt an external granule cell-like phenotype in the absence of Ptf1a transcription factor expression. Proc Natl Acad Sci U S A 104: 5193-5198.
-
(2007)
Proc Natl Acad Sci U S A
, vol.104
, pp. 5193-5198
-
-
Pascual, M.1
Abasolo, I.2
Mingorance-Le Meur, A.3
Martinez, A.4
Del Rio, J.A.5
-
43
-
-
33745214464
-
Ectopic pancreas formation in Hes1 -knockout mice reveals plasticity of endodermal progenitors of the gut, bile duct, and pancreas
-
Fukuda A, Kawaguchi Y, Furuyama K, Kodama S, Horiguchi M, et al. (2006) Ectopic pancreas formation in Hes1-knockout mice reveals plasticity of endodermal progenitors of the gut, bile duct, and pancreas. J Clin Invest 116: 1484-1493.
-
(2006)
J Clin Invest
, vol.116
, pp. 1484-1493
-
-
Fukuda, A.1
Kawaguchi, Y.2
Furuyama, K.3
Kodama, S.4
Horiguchi, M.5
-
44
-
-
0031870637
-
Genetic interactions suggest that Danforth's short tail (Sd) is a gain-of-function mutation
-
Zachgo J, Korn R, Gossler A, (1998) Genetic interactions suggest that Danforth's short tail (Sd) is a gain-of-function mutation. Dev Genet 23: 86-96.
-
(1998)
Dev Genet
, vol.23
, pp. 86-96
-
-
Zachgo, J.1
Korn, R.2
Gossler, A.3
-
45
-
-
11144339384
-
Long-range control of gene expression: emerging mechanisms and disruption in disease
-
Kleinjan DA, van Heyningen V, (2005) Long-range control of gene expression: emerging mechanisms and disruption in disease. Am J Hum Genet 76: 8-32.
-
(2005)
Am J Hum Genet
, vol.76
, pp. 8-32
-
-
Kleinjan, D.A.1
van Heyningen, V.2
-
46
-
-
20044366725
-
Highly conserved non-coding sequences are associated with vertebrate development
-
doi: 10.1371/journal.pbio.0030007
-
Woolfe A, Goodson M, Goode DK, Snell P, McEwen GK, et al. (2005) Highly conserved non-coding sequences are associated with vertebrate development. PLoS Biol 3: e7 doi:10.1371/journal.pbio.0030007.
-
(2005)
PLoS Biol
, vol.3
-
-
Woolfe, A.1
Goodson, M.2
Goode, D.K.3
Snell, P.4
McEwen, G.K.5
-
47
-
-
39049141215
-
Organization of conserved elements near key developmental regulators in vertebrate genomes
-
Woolfe A, Elgar G, (2008) Organization of conserved elements near key developmental regulators in vertebrate genomes. Adv Genet 61: 307-338.
-
(2008)
Adv Genet
, vol.61
, pp. 307-338
-
-
Woolfe, A.1
Elgar, G.2
-
48
-
-
84870891672
-
Copy Number Disorders are a Common Cause of Congenital Kidney Malformations
-
Sanna-Cherchi S, Kiryluk K, Burgess K, Bodria M, Sampson M, et al. (2012) Copy Number Disorders are a Common Cause of Congenital Kidney Malformations. Am J Hum Genet (in press).
-
(2012)
Am J Hum Genet
-
-
Sanna-Cherchi, S.1
Kiryluk, K.2
Burgess, K.3
Bodria, M.4
Sampson, M.5
-
49
-
-
80052851950
-
Mouse genomic variation and its effect on phenotypes and gene regulation
-
Keane TM, Goodstadt L, Danecek P, White MA, Wong K, et al. (2011) Mouse genomic variation and its effect on phenotypes and gene regulation. Nature 477: 289-294.
-
(2011)
Nature
, vol.477
, pp. 289-294
-
-
Keane, T.M.1
Goodstadt, L.2
Danecek, P.3
White, M.A.4
Wong, K.5
-
50
-
-
33750831582
-
Annotation, submission and screening of repetitive elements in Repbase: RepbaseSubmitter and Censor
-
Kohany O, Gentles AJ, Hankus L, Jurka J, (2006) Annotation, submission and screening of repetitive elements in Repbase: RepbaseSubmitter and Censor. BMC Bioinformatics 7: 474.
-
(2006)
BMC Bioinformatics
, vol.7
, pp. 474
-
-
Kohany, O.1
Gentles, A.J.2
Hankus, L.3
Jurka, J.4
-
51
-
-
0027445532
-
Detection of messenger RNA by in situ hybridization to tissue sections and whole mounts
-
Wilkinson DG, Nieto MA, (1993) Detection of messenger RNA by in situ hybridization to tissue sections and whole mounts. Methods Enzymol 225: 361-373.
-
(1993)
Methods Enzymol
, vol.225
, pp. 361-373
-
-
Wilkinson, D.G.1
Nieto, M.A.2
|