-
1
-
-
0017121616
-
The incidence of birthmarks in the neonate
-
Jacobs AH, Walton RG. The incidence of birthmarks in the neonate. Pediatrics 1976 58 : 218 22.
-
(1976)
Pediatrics
, vol.58
, pp. 218-22
-
-
Jacobs, A.H.1
Walton, R.G.2
-
3
-
-
0042632780
-
Vascular malformations: Localized defects in vascular morphogenesis
-
Brouillard P, Vikkula M. Vascular malformations: localized defects in vascular morphogenesis. Clin Genet 2003 63 : 340 51.
-
(2003)
Clin Genet
, vol.63
, pp. 340-51
-
-
Brouillard, P.1
Vikkula, M.2
-
4
-
-
0347362524
-
Capillary malformation-arteriovenous malformation, a new clinical and genetic disorder caused by RASA1 mutations
-
Eerola I, Boon LM, Mulliken JB et al. Capillary malformation- arteriovenous malformation, a new clinical and genetic disorder caused by RASA1 mutations. Am J Hum Genet 2003 73 : 1240 9.
-
(2003)
Am J Hum Genet
, vol.73
, pp. 1240-9
-
-
Eerola, I.1
Boon, L.M.2
Mulliken, J.B.3
-
5
-
-
0024212303
-
Molecular cloning of two types of GAP complementary DNA from human placenta
-
Trahey M, Wong G, Halenbeck R et al. Molecular cloning of two types of GAP complementary DNA from human placenta. Science 1988 242 : 1697 700.
-
(1988)
Science
, vol.242
, pp. 1697-700
-
-
Trahey, M.1
Wong, G.2
Halenbeck, R.3
-
6
-
-
0028788570
-
Vascular system defects and neuronal apoptosis in mice lacking ras GTPase-activating protein
-
Henkemeyer M, Rossi DJ, Holmyard DP et al. Vascular system defects and neuronal apoptosis in mice lacking ras GTPase-activating protein. Nature 1995 377 : 695 701.
-
(1995)
Nature
, vol.377
, pp. 695-701
-
-
Henkemeyer, M.1
Rossi, D.J.2
Holmyard, D.P.3
-
7
-
-
0034678368
-
Role of p120 Ras-GAP in directed cell movement
-
Kulkarni SV, Gish G, van der Geer P et al. Role of p120 Ras-GAP in directed cell movement. J Cell Biol 2000 149 : 457 70.
-
(2000)
J Cell Biol
, vol.149
, pp. 457-70
-
-
Kulkarni, S.V.1
Gish, G.2
Van Der Geer, P.3
-
8
-
-
0242266952
-
Denaturing high-performance liquid chromatography for the detection of mutations and polymorphisms in UBE3A
-
Bercovich D, Beaudet AL. Denaturing high-performance liquid chromatography for the detection of mutations and polymorphisms in UBE3A. Genet Test 2003 7 : 189 94.
-
(2003)
Genet Test
, vol.7
, pp. 189-94
-
-
Bercovich, D.1
Beaudet, A.L.2
-
9
-
-
33749491894
-
Vascular update: Morphogenesis, tumors, malformations, and molecular dimensions
-
Cohen MM Jr. Vascular update: morphogenesis, tumors, malformations, and molecular dimensions. Am J Med Genet A 2006 140 : 2013 38.
-
(2006)
Am J Med Genet a
, vol.140
, pp. 2013-38
-
-
Cohen Jr., M.M.1
-
10
-
-
0024394433
-
Age-related clinical profile of hereditary hemorrhagic telangiectasia in an epidemiologically recruited population
-
Plauchu H, de Chadarevian JP, Bideau A et al. Age-related clinical profile of hereditary hemorrhagic telangiectasia in an epidemiologically recruited population. Am J Med Genet 1989 32 : 291 7.
-
(1989)
Am J Med Genet
, vol.32
, pp. 291-7
-
-
Plauchu, H.1
De Chadarevian, J.P.2
Bideau, A.3
-
11
-
-
0030050973
-
Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2
-
Johnson DW, Berg JN, Baldwin MA et al. Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2. Nat Genet 1996 13 : 189 95.
-
(1996)
Nat Genet
, vol.13
, pp. 189-95
-
-
Johnson, D.W.1
Berg, J.N.2
Baldwin, M.A.3
-
12
-
-
0028171579
-
Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1
-
McAllister KA, Grogg KM, Johnson DW et al. Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1. Nat Genet 1994 8 : 345 51.
-
(1994)
Nat Genet
, vol.8
, pp. 345-51
-
-
McAllister, K.A.1
Grogg, K.M.2
Johnson, D.W.3
-
13
-
-
0030460775
-
Vascular dysmorphogenesis caused by an activating mutation in the receptor tyrosine kinase TIE2
-
Vikkula M, Boon LM, Carraway KL 3rd. et al. Vascular dysmorphogenesis caused by an activating mutation in the receptor tyrosine kinase TIE2. Cell 1996 87 : 1181 90.
-
(1996)
Cell
, vol.87
, pp. 1181-90
-
-
Vikkula, M.1
Boon, L.M.2
Carraway III, K.L.3
-
14
-
-
0036201378
-
Mutations in a novel factor, glomulin, are responsible for glomuvenous malformations ('glomangiomas')
-
Brouillard P, Boon LM, Mulliken JB et al. Mutations in a novel factor, glomulin, are responsible for glomuvenous malformations ('glomangiomas'). Am J Hum Genet 2002 70 : 866 74.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 866-74
-
-
Brouillard, P.1
Boon, L.M.2
Mulliken, J.B.3
|