-
1
-
-
0025017752
-
Two 46,XX, t(X;Y) females with linear skin defects and congenital microphtalmia: A new syndrome at Xp22.3
-
Al Gazali LI, Mueller RF, Caine A, Antoniou A, Mc Cartney A, Fitchett M, et al. (1990). Two 46,XX, t(X;Y) females with linear skin defects and congenital microphtalmia: a new syndrome at Xp22.3. J Med Genet 27:59-63.
-
(1990)
J Med Genet
, vol.27
, pp. 59-63
-
-
Al Gazali, L.I.1
Mueller, R.F.2
Caine, A.3
Antoniou, A.4
McCartney, A.5
Fitchett, M.6
-
2
-
-
0016764842
-
Das Goltz-Gorlin-Syndrom: Übersicht und kasuistic
-
Braun-Falco O, Hofmann C (1975). Das Goltz-Gorlin-Syndrom: Übersicht und kasuistic. Hautarzt 26:393-400.
-
(1975)
Hautarzt
, vol.26
, pp. 393-400
-
-
Braun-Falco, O.1
Hofmann, C.2
-
3
-
-
0026686762
-
Focal dermal hypoplasia syndrome in a male patient. Report of a case and histologic and immunohistochemical studies
-
Buchner SA, Itin P (1992). Focal dermal hypoplasia syndrome in a male patient. Report of a case and histologic and immunohistochemical studies. Arch Dermatol 128:1078-1082.
-
(1992)
Arch Dermatol
, vol.128
, pp. 1078-1082
-
-
Buchner, S.A.1
Itin, P.2
-
5
-
-
0018148266
-
Focal dermal hypoplasia (Goltz syndrome)
-
Derks B, Gericke GS, Louw M (1978). Focal dermal hypoplasia (Goltz syndrome). S Afr Med J 54:27-29.
-
(1978)
S Afr Med J
, vol.54
, pp. 27-29
-
-
Derks, B.1
Gericke, G.S.2
Louw, M.3
-
6
-
-
13244256768
-
Developmental toxicity studies with glyphosate and selected surfactants in rats
-
Farmer DR, Kaempfe TA, Heydens WF (2000). Developmental toxicity studies with glyphosate and selected surfactants in rats. Teratology 61:446.
-
(2000)
Teratology
, vol.61
, pp. 446
-
-
Farmer, D.R.1
Kaempfe, T.A.2
Heydens, W.F.3
-
7
-
-
0015307081
-
Goltz's syndrome
-
Ferrara A (1972). Goltz's syndrome. Am J Dis Child 123:263.
-
(1972)
Am J Dis Child
, vol.123
, pp. 263
-
-
Ferrara, A.1
-
8
-
-
0001232401
-
Provisional deletion mapping of the focal dermal hypoplasia (FDH) gene to Xp22.31
-
Friedman PA, Rao KW, Teplin SW, Aylsworth AS (1988). Provisional deletion mapping of the focal dermal hypoplasia (FDH) gene to Xp22.31. Am J Hum Genet 43:A50.
-
(1988)
Am J Hum Genet
, vol.43
-
-
Friedman, P.A.1
Rao, K.W.2
Teplin, S.W.3
Aylsworth, A.S.4
-
10
-
-
0026738894
-
Focal dermal hypoplasia syndrome: An update
-
Goltz RW (1992). Focal dermal hypoplasia syndrome: an update. Arch Dermatol 128:1108-1111.
-
(1992)
Arch Dermatol
, vol.128
, pp. 1108-1111
-
-
Goltz, R.W.1
-
11
-
-
0014704403
-
Focal dermal hypoplasia syndrome. A review of the literature and report of two cases
-
Goltz RW, Henderson RR, Hitch JM, Ott JE (1970). Focal dermal hypoplasia syndrome. A review of the literature and report of two cases. Arch Dermatol 101:1-11.
-
(1970)
Arch Dermatol
, vol.101
, pp. 1-11
-
-
Goltz, R.W.1
Henderson, R.R.2
Hitch, J.M.3
Ott, J.E.4
-
13
-
-
0344410719
-
Focal dermal hypoplasia (Goltz-Gorlin syndrome)
-
Gorlin RJ, Cohen MM. Jr, Hennekan RCM. New York
-
Gorlin RJ, Cohen MM. Jr, Hennekan RCM (2001). Focal dermal hypoplasia (Goltz-Gorlin syndrome). In: Gorlin RJ, Cohen MM. Jr, Hennekan RCM. Syndromes of Head and Neck. New York, pp. 571-576.
-
(2001)
Syndromes of Head and Neck
, pp. 571-576
-
-
Gorlin, R.J.1
Cohen Jr., M.M.2
Hennekan, R.C.M.3
-
15
-
-
0037100087
-
Probable identity of Goltz syndrome and Van Allen-Myhre syndrome: Evidence from phenotypic evolution
-
Hancock S, Pryde P, Fong C, Brazy JE, Stewart K, Favour A, et al. (2002). Probable identity of Goltz syndrome and Van Allen-Myhre syndrome: Evidence from phenotypic evolution. Am J Med Genet 110:370-379.
-
(2002)
Am J Med Genet
, vol.110
, pp. 370-379
-
-
Hancock, S.1
Pryde, P.2
Fong, C.3
Brazy, J.E.4
Stewart, K.5
Favour, A.6
-
16
-
-
0023319298
-
Lethal genes surviving by mosaicism: A possible explanation for sporadic birth defects involving the skin
-
Happle R (1987). Lethal genes surviving by mosaicism: A possible explanation for sporadic birth defects involving the skin. J Am Acad Dermatol 16:899-906.
-
(1987)
J Am Acad Dermatol
, vol.16
, pp. 899-906
-
-
Happle, R.1
-
17
-
-
0029925048
-
Focal dermal hypoplasia (Goltz syndrome) associated with intestinal malrotation and mediastinal dextroposition
-
Irvine AD, Stewart FJ, Bingham EA, Nevin NC, Booston VE (1996). Focal dermal hypoplasia (Goltz syndrome) associated with intestinal malrotation and mediastinal dextroposition. Am J Med Genet 62:231-215.
-
(1996)
Am J Med Genet
, vol.62
, pp. 231-215
-
-
Irvine, A.D.1
Stewart, F.J.2
Bingham, E.A.3
Nevin, N.C.4
Booston, V.E.5
-
18
-
-
13244262552
-
An evaluation of the genotoxic potential of glyphosate
-
Li AP, Long TJ (1988). An evaluation of the genotoxic potential of glyphosate. Arch Biochem Biophys 260:85-93.
-
(1988)
Arch Biochem Biophys
, vol.260
, pp. 85-93
-
-
Li, A.P.1
Long, T.J.2
-
19
-
-
0017342364
-
Kasuistischer beitrag zum Goltz-Gorlin syndrom
-
Rodermund OE, Heiusmann D (1977). Kasuistischer beitrag zum Goltz-Gorlin syndrom. Hautarzt 28:37-38.
-
(1977)
Hautarzt
, vol.28
, pp. 37-38
-
-
Rodermund, O.E.1
Heiusmann, D.2
-
20
-
-
0021751372
-
Syndrome de Goltz: Deux cas féminins
-
Stalder JF, Delaire J, David A, Cohen JY, Le Pape A (1984). Syndrome de Goltz: deux cas féminins. Ann Dermatol Venereol 111:833-834.
-
(1984)
Ann Dermatol Venereol
, vol.111
, pp. 833-834
-
-
Stalder, J.F.1
Delaire, J.2
David, A.3
Cohen, J.Y.4
Le Pape, A.5
-
22
-
-
0016365218
-
A case of focal dermal hypoplasia syndrome (Goltz) with bilateral cheil-gnatho-palatoschisis
-
Valerius NH (1974). A case of focal dermal hypoplasia syndrome (Goltz) with bilateral cheil-gnatho-palatoschisis. Acta Paediatr Scand 63:287-288.
-
(1974)
Acta Paediatr Scand
, vol.63
, pp. 287-288
-
-
Valerius, N.H.1
-
23
-
-
0025978279
-
New multiple congenital anomalies syndrome in a stillborn infant of consanguinous parents and a prediabetic pregnancy
-
Van Allen MI, Myhre S (1991). New multiple congenital anomalies syndrome in a stillborn infant of consanguinous parents and a prediabetic pregnancy. Am J Med Genet 38:523-528.
-
(1991)
Am J Med Genet
, vol.38
, pp. 523-528
-
-
Van Allen, M.I.1
Myhre, S.2
-
24
-
-
0020518307
-
X-linked dominant inherited diseases with lethality in hemizygous males
-
Wettke-Schafer R, Kantner G (1983). X-linked dominant inherited diseases with lethality in hemizygous males. Hum Genet 64:1-23.
-
(1983)
Hum Genet
, vol.64
, pp. 1-23
-
-
Wettke-Schafer, R.1
Kantner, G.2
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