-
8
-
-
13344259999
-
A comprehensive genetic map of the human genome based on 5,264 microsatellites
-
(1996)
Nature
, vol.380
, pp. 152-154
-
-
Dib, C.1
Fauré, S.2
Fizames, C.3
Samson, D.4
Drouot, N.5
Vignal, A.6
Millasseau, P.7
Marc, S.8
Hazan, J.9
Seboun, E.10
Lathrop, M.11
Gyapay, G.12
Morrissette, J.13
Weissenbach, J.14
-
13
-
-
8944233367
-
Duplication of a gene-rich cluster between 16p11.1 and Xq28: A novel pericentromeric-directed mechanism for paralogous genome evolution
-
(1996)
Hum Mol Genet
, vol.5
, pp. 899-912
-
-
Eichler, E.E.1
Lu, F.2
Shen, Y.3
Antonacci, R.4
Jurecic, V.5
Doggett, N.A.6
Moyzis, R.K.7
Baldini, A.8
Gibbs, R.A.9
Nelson, D.L.10
-
14
-
-
0033927869
-
Segregation analysis in Shwachman-Diamond syndrome: Evidence for recessive inheritance
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1413-1416
-
-
Ginzberg, H.1
Shin, J.2
Ellis, L.3
Goobie, S.4
Morrison, J.5
Corey, M.6
Durie, P.R.7
Rommens, J.M.8
-
15
-
-
0033497428
-
Shwachman syndrome: Phenotypic manifestations of sibling sets and isolated cases in a large patient cohort are similar
-
(1999)
J Pediatr
, vol.135
, pp. 81-88
-
-
Ginzberg, H.1
Shin, J.2
Ellis, L.3
Morrison, J.4
Ip, W.5
Dror, Y.6
Freedman, M.7
Heitlinger, L.A.8
Belt, M.A.9
Corey, M.10
Rommens, J.M.11
Durie, P.R.12
-
16
-
-
0032999951
-
Exclusion of linkage of Shwachman-Diamond syndrome to chromosome regions 6q and 12q implicated by a de novo translocation
-
(1999)
Am J Med Genet
, vol.85
, pp. 171-174
-
-
Goobie, S.1
Morrison, J.2
Ginzberg, H.3
Ellis, L.4
Corey, M.5
Masuno, M.6
Imaizumi, K.7
Kuroki, Y.8
Fujiwara, T.M.9
Morgan, K.10
Durie, P.R.11
Rommens, J.M.12
-
18
-
-
0002303695
-
PCR methods of genotyping
-
Dracopoli NC, Haines JL, Korf BR, Moir DT, Morton CC, Seidman CE, Seidman JG, Smith DR, Boyle AL (eds) Current protocols in human genetics. John Wiley & Sons, New York
-
(1997)
, pp. 251-2523
-
-
Hudson, T.J.1
Clark, C.D.2
Gschwend, M.3
Justice-Higgins, E.4
-
20
-
-
0032791181
-
Cloning of translocation breakpoints associated with Shwachman syndrome and identification of a candidate gene
-
(1999)
Clin Genet
, vol.55
, pp. 466-472
-
-
Ikegawa, S.1
Masuno, M.2
Kumano, Y.3
Okawa, A.4
Isomura, M.5
Koyama, K.6
Okui, K.7
Makita, Y.8
Sasaki, M.9
Kohdera, U.10
Okuda, M.11
Koyama, H.12
Ohashi, H.13
Tajiri, H.14
Imaizumi, K.15
Nakamura, Y.16
-
21
-
-
0032928889
-
Sequences flanking the centromere of human chromosome 10 are a complex patchwork of arm-specific sequences, stable duplications and unstable sequences with homologies to telomeric and other centromeric locations
-
(1999)
Hum Mol Genet
, vol.8
, pp. 205-215
-
-
Jackson, M.S.1
Rocchi, M.2
Thompson, G.3
Hearn, T.4
Crosier, M.5
Guy, J.6
Kirk, D.7
Mulligan, L.8
Ricco, A.9
Piccininni, S.10
Marzella, R.11
Viggiano, L.12
Archidiacono, N.13
-
30
-
-
0033785246
-
Isochromosome (7)(q10) in Shwachman Syndrome without MDS/AML and role of chromosome 7 anomalies in myeloproliferative disorders
-
(2000)
Cancer Genet Cytogenet
, vol.121
, pp. 167-171
-
-
Maserati, E.1
Minelli, A.2
Olivieri, C.3
Bonvini, L.4
Marchi, A.5
Bozzola, M.6
Danesino, C.7
Scappaticci, S.8
Pasquali, F.9
-
35
-
-
0032231916
-
Familial eosinophilia maps to the cytokine gene cluster on human chromosomal region 5q31-q33
-
(1998)
Am J Hum Genet
, vol.63
, pp. 1086-1094
-
-
Rioux, J.D.1
Stone, V.A.2
Daly, M.J.3
Cargill, M.4
Green, T.5
Nguyen, H.6
Nutman, T.7
Zimmerman, P.A.8
Tucker, M.A.9
Hudson, T.10
Goldstein, A.M.11
Lander, E.12
Lin, A.Y.13
-
39
-
-
0014635815
-
The syndrome of exocrine pancreatic insufficiency, neutropenia, metaphyseal dysostosis and dwarfism
-
(1969)
Helvetica Paediatr Acta
, vol.24
, pp. 547-575
-
-
Shmerling, D.H.1
Prader, A.2
Hitzig, W.H.3
Giedion, A.4
Hadorn, Z.B.5
Kühni, M.6
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