-
1
-
-
0034672337
-
Molecular characterization of a case of atransferrinemia
-
Beutler E, Gelbart T, Lee P, Trevino R, Fernandez MA, Fairbanks VF. Molecular characterization of a case of atransferrinemia. Blood. 2000;96:4071-4074.
-
(2000)
Blood
, vol.96
, pp. 4071-4074
-
-
Beutler, E.1
Gelbart, T.2
Lee, P.3
Trevino, R.4
Fernandez, M.A.5
Fairbanks, V.F.6
-
2
-
-
0015543930
-
Congenital hypochromic microcytic anaemia with iron overload of the liver and hyperferraemia
-
Stavem P, Saltvedt E, Elgjo K, Rootwelt K. Congenital hypochromic microcytic anaemia with iron overload of the liver and hyperferraemia. Scand J Haematol. 1973;10:153-160.
-
(1973)
Scand J Haematol
, vol.10
, pp. 153-160
-
-
Stavem, P.1
Saltvedt, E.2
Elgjo, K.3
Rootwelt, K.4
-
3
-
-
0034254752
-
The molecular defect in hypotransferrinemic mice
-
Trenor CC, Campagna DR, Sellers VM, Andrews NC, Fleming MD. The molecular defect in hypotransferrinemic mice. Blood. 2000;96:1113-1118.
-
(2000)
Blood
, vol.96
, pp. 1113-1118
-
-
Trenor, C.C.1
Campagna, D.R.2
Sellers, V.M.3
Andrews, N.C.4
Fleming, M.D.5
-
4
-
-
0031612929
-
Recommendations for a nomenclature system for human gene mutations: Nomenclature Working Group
-
Antonarakis SE. Recommendations for a nomenclature system for human gene mutations: Nomenclature Working Group. Hum Mutat. 1998;11:1-3.
-
(1998)
Hum Mutat
, vol.11
, pp. 1-3
-
-
Antonarakis, S.E.1
-
5
-
-
0033987736
-
Mutation nomenclature extensions and suggestions to describe complex mutations: A discussion
-
den Dunnen JT, Antonarakis SE. Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion. Hum Mutat. 2000;15:7-12.
-
(2000)
Hum Mutat
, vol.15
, pp. 7-12
-
-
Den Dunnen, J.T.1
Antonarakis, S.E.2
-
7
-
-
0027360042
-
Studies on familial hypotransferrinemia: Unique clinical course and molecular pathology
-
Hayashi A, Wada Y, Suzuki T, Shimizu A. Studies on familial hypotransferrinemia: unique clinical course and molecular pathology. Am J Hum Genet. 1993; 53:201-213.
-
(1993)
Am J Hum Genet
, vol.53
, pp. 201-213
-
-
Hayashi, A.1
Wada, Y.2
Suzuki, T.3
Shimizu, A.4
-
8
-
-
0036308217
-
Molecular analysis of the transferrin gene in a patient with hereditary hypotransferrinemia
-
Asada-Senju M, Maeda T, Sakata T, Hayashi A, Suzuki T. Molecular analysis of the transferrin gene in a patient with hereditary hypotransferrinemia. J Hum Genet. 2002;47:355-359.
-
(2002)
J Hum Genet
, vol.47
, pp. 355-359
-
-
Asada-Senju, M.1
Maeda, T.2
Sakata, T.3
Hayashi, A.4
Suzuki, T.5
-
9
-
-
0014340744
-
Kongenitálna atransferinémia u 11-mesačného diet'at'a
-
Čáp J, Lehotská V, Mayerová A. Kongenitálna atransferinémia u 11-mesačného diet'at'a. Cesk Pediatr. 1968;23:1020-1025.
-
(1968)
Cesk Pediatr
, vol.23
, pp. 1020-1025
-
-
Čáp, J.1
Lehotská, V.2
Mayerová, A.3
-
11
-
-
4944225586
-
Kongenitale atransferrinämie: Klinische beobachtungen während einer 18jährigen substitution mit humantransferrin
-
Hromec A, Čáp J, Schwick HG. Kongenitale Atransferrinämie: Klinische Beobachtungen während einer 18jährigen Substitution mit Humantransferrin. Pädiatr Praxis. 1989;38:633-637.
-
(1989)
Pädiatr Praxis
, vol.38
, pp. 633-637
-
-
Hromec, A.1
Čáp, J.2
Schwick, H.G.3
-
12
-
-
0028766424
-
Kongenitale atransferrinämie
-
Hromec A, Payer J Jr, Killinger Z, Rybär I, Rovensky J. Kongenitale Atransferrinämie. Dtsch Med Wochenschr. 1994;119:663-666.
-
(1994)
Dtsch Med Wochenschr
, vol.119
, pp. 663-666
-
-
Hromec, A.1
Payer Jr., J.2
Killinger, Z.3
Rybär, I.4
Rovensky, J.5
|