متلازمة شواخمان دايموند (Arabic Wikipedia)

Analysis of information sources in references of the Wikipedia article "متلازمة شواخمان دايموند" in Arabic language version.

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11nih.gov

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9doi.org

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3archive.org

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3semanticscholar.org

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archive.org

Shwachman H، Diamond LK، Oski FA، Khaw KT (1964). "The syndrome of pancreatic insufficiency and bone marrow dysfunction". J Pediatr. ج. 65: 645–63. DOI:10.1016/S0022-3476(64)80150-5. PMID:14221166.
Goobie، S؛ Popovic, M؛ Morrison, J؛ Ellis, L؛ Ginzberg, H؛ Boocock, GR؛ Ehtesham, N؛ Bétard, C؛ Brewer, CG؛ Roslin, NM؛ Hudson, TJ؛ Morgan, K؛ Fujiwara, TM؛ Durie, PR؛ Rommens, JM (أبريل 2001). "Shwachman-Diamond syndrome with exocrine pancreatic dysfunction and bone marrow failure maps to the centromeric region of chromosome 7". American Journal of Human Genetics. ج. 68 ع. 4: 1048–54. DOI:10.1086/319505. PMC:1275624. PMID:11254457.
Zhang S، Shi M، Hui CC، Rommens، JM (2006). "Loss of the mouse ortholog of the shwachman-diamond syndrome gene (Sbds) results in early embryonic lethality". Mol Cell Biol. ج. 26 ع. 17: 6656–63. DOI:10.1128/MCB.00091-06. PMC:1592835. PMID:16914746.

books.google.com

Orkin، Stuart H.؛ Nathan، David G.؛ Ginsburg، David؛ A. Thomas Look (2009). Nathan and Oski's hematology of infancy and childhood. Elsevier Health Sciences. ص. 344–. ISBN:978-1-4160-3430-8. مؤرشف من الأصل في 2021-10-05. اطلع عليه بتاريخ 2011-08-08.

doi.org

Shammas C، Menne TF، Hilcenko C، Michell SR، Goyenechea B، Boocock GR، Durie PR، Rommens JM، Warren AJ (2005). "Structural and mutational analysis of the SBDS protein family. Insight into the leukemia-associated Shwachman–Diamond Syndrome". J Biol Chem. ج. 280 ع. 19: 19221–9. DOI:10.1074/jbc.M414656200. PMID:15701631.
Hassan، Fauziya؛ Byersdorfer, Craig؛ Nasr, Samya (1 يناير 2010). "Severe Shwachman-Diamond syndrome and associated CF carrier mutations". Respiratory Medicine CME. ج. 3 ع. 1: 18–19. DOI:10.1016/j.rmedc.2009.02.001.
Shwachman H، Diamond LK، Oski FA، Khaw KT (1964). "The syndrome of pancreatic insufficiency and bone marrow dysfunction". J Pediatr. ج. 65: 645–63. DOI:10.1016/S0022-3476(64)80150-5. PMID:14221166.
Shammas C، Menne TF، Hilcenko C، Michell SR، Goyenechea B، Boocock GR، Durie PR، Rommens JM، Warren AJ (2005). "Structural and mutational analysis of the SBDS protein family. Insight into the leukemia-associated Shwachman–Diamond Syndrome". J Biol Chem. ج. 280 ع. 19: 19221–9. DOI:10.1074/jbc.M414656200. PMID:15701631. S2CID:8011896.
Austin KM، Leary RJ، Shimamura A (2005). "The Shwachman–Diamond SBDS protein localizes to the nucleolus". Blood. ج. 106 ع. 4: 1253–8. DOI:10.1182/blood-2005-02-0807. PMC:1895203. PMID:15860664.
Makitie O، Ellis L، Durie PR، Morrison JA، Sochett EB، Rommens JM، Cole WG (2004). "Skeletal phenotype in patients with Shwachman–Diamond syndrome and mutations in SBDS". Clin Genet. ج. 65 ع. 2: 101–12. DOI:10.1111/j.0009-9163.2004.00198.x. PMID:14984468. S2CID:34964226.
Goobie، S؛ Popovic, M؛ Morrison, J؛ Ellis, L؛ Ginzberg, H؛ Boocock, GR؛ Ehtesham, N؛ Bétard, C؛ Brewer, CG؛ Roslin, NM؛ Hudson, TJ؛ Morgan, K؛ Fujiwara, TM؛ Durie, PR؛ Rommens, JM (أبريل 2001). "Shwachman-Diamond syndrome with exocrine pancreatic dysfunction and bone marrow failure maps to the centromeric region of chromosome 7". American Journal of Human Genetics. ج. 68 ع. 4: 1048–54. DOI:10.1086/319505. PMC:1275624. PMID:11254457.
Popovic، M؛ Goobie, S؛ Morrison, J؛ Ellis, L؛ Ehtesham, N؛ Richards, N؛ Boocock, G؛ Durie, PR؛ Rommens, JM (أبريل 2002). "Fine mapping of the locus for Shwachman-Diamond syndrome at 7q11, identification of shared disease haplotypes, and exclusion of TPST1 as a candidate gene". European Journal of Human Genetics. ج. 10 ع. 4: 250–8. DOI:10.1038/sj.ejhg.5200798. PMID:12032733. S2CID:12667823.
Zhang S، Shi M، Hui CC، Rommens، JM (2006). "Loss of the mouse ortholog of the shwachman-diamond syndrome gene (Sbds) results in early embryonic lethality". Mol Cell Biol. ج. 26 ع. 17: 6656–63. DOI:10.1128/MCB.00091-06. PMC:1592835. PMID:16914746.

nih.gov

pubmed.ncbi.nlm.nih.gov

Shammas C، Menne TF، Hilcenko C، Michell SR، Goyenechea B، Boocock GR، Durie PR، Rommens JM، Warren AJ (2005). "Structural and mutational analysis of the SBDS protein family. Insight into the leukemia-associated Shwachman–Diamond Syndrome". J Biol Chem. ج. 280 ع. 19: 19221–9. DOI:10.1074/jbc.M414656200. PMID:15701631.
Shwachman H، Diamond LK، Oski FA، Khaw KT (1964). "The syndrome of pancreatic insufficiency and bone marrow dysfunction". J Pediatr. ج. 65: 645–63. DOI:10.1016/S0022-3476(64)80150-5. PMID:14221166.
Shammas C، Menne TF، Hilcenko C، Michell SR، Goyenechea B، Boocock GR، Durie PR، Rommens JM، Warren AJ (2005). "Structural and mutational analysis of the SBDS protein family. Insight into the leukemia-associated Shwachman–Diamond Syndrome". J Biol Chem. ج. 280 ع. 19: 19221–9. DOI:10.1074/jbc.M414656200. PMID:15701631. S2CID:8011896.
Austin KM، Leary RJ، Shimamura A (2005). "The Shwachman–Diamond SBDS protein localizes to the nucleolus". Blood. ج. 106 ع. 4: 1253–8. DOI:10.1182/blood-2005-02-0807. PMC:1895203. PMID:15860664.
Makitie O، Ellis L، Durie PR، Morrison JA، Sochett EB، Rommens JM، Cole WG (2004). "Skeletal phenotype in patients with Shwachman–Diamond syndrome and mutations in SBDS". Clin Genet. ج. 65 ع. 2: 101–12. DOI:10.1111/j.0009-9163.2004.00198.x. PMID:14984468. S2CID:34964226.
Goobie، S؛ Popovic, M؛ Morrison, J؛ Ellis, L؛ Ginzberg, H؛ Boocock, GR؛ Ehtesham, N؛ Bétard, C؛ Brewer, CG؛ Roslin, NM؛ Hudson, TJ؛ Morgan, K؛ Fujiwara, TM؛ Durie, PR؛ Rommens, JM (أبريل 2001). "Shwachman-Diamond syndrome with exocrine pancreatic dysfunction and bone marrow failure maps to the centromeric region of chromosome 7". American Journal of Human Genetics. ج. 68 ع. 4: 1048–54. DOI:10.1086/319505. PMC:1275624. PMID:11254457.
Popovic، M؛ Goobie, S؛ Morrison, J؛ Ellis, L؛ Ehtesham, N؛ Richards, N؛ Boocock, G؛ Durie, PR؛ Rommens, JM (أبريل 2002). "Fine mapping of the locus for Shwachman-Diamond syndrome at 7q11, identification of shared disease haplotypes, and exclusion of TPST1 as a candidate gene". European Journal of Human Genetics. ج. 10 ع. 4: 250–8. DOI:10.1038/sj.ejhg.5200798. PMID:12032733. S2CID:12667823.
Zhang S، Shi M، Hui CC، Rommens، JM (2006). "Loss of the mouse ortholog of the shwachman-diamond syndrome gene (Sbds) results in early embryonic lethality". Mol Cell Biol. ج. 26 ع. 17: 6656–63. DOI:10.1128/MCB.00091-06. PMC:1592835. PMID:16914746.

ncbi.nlm.nih.gov

Austin KM، Leary RJ، Shimamura A (2005). "The Shwachman–Diamond SBDS protein localizes to the nucleolus". Blood. ج. 106 ع. 4: 1253–8. DOI:10.1182/blood-2005-02-0807. PMC:1895203. PMID:15860664.
Goobie، S؛ Popovic, M؛ Morrison, J؛ Ellis, L؛ Ginzberg, H؛ Boocock, GR؛ Ehtesham, N؛ Bétard, C؛ Brewer, CG؛ Roslin, NM؛ Hudson, TJ؛ Morgan, K؛ Fujiwara, TM؛ Durie, PR؛ Rommens, JM (أبريل 2001). "Shwachman-Diamond syndrome with exocrine pancreatic dysfunction and bone marrow failure maps to the centromeric region of chromosome 7". American Journal of Human Genetics. ج. 68 ع. 4: 1048–54. DOI:10.1086/319505. PMC:1275624. PMID:11254457.
Zhang S، Shi M، Hui CC، Rommens، JM (2006). "Loss of the mouse ortholog of the shwachman-diamond syndrome gene (Sbds) results in early embryonic lethality". Mol Cell Biol. ج. 26 ع. 17: 6656–63. DOI:10.1128/MCB.00091-06. PMC:1592835. PMID:16914746.

semanticscholar.org

api.semanticscholar.org

Shammas C، Menne TF، Hilcenko C، Michell SR، Goyenechea B، Boocock GR، Durie PR، Rommens JM، Warren AJ (2005). "Structural and mutational analysis of the SBDS protein family. Insight into the leukemia-associated Shwachman–Diamond Syndrome". J Biol Chem. ج. 280 ع. 19: 19221–9. DOI:10.1074/jbc.M414656200. PMID:15701631. S2CID:8011896.
Makitie O، Ellis L، Durie PR، Morrison JA، Sochett EB، Rommens JM، Cole WG (2004). "Skeletal phenotype in patients with Shwachman–Diamond syndrome and mutations in SBDS". Clin Genet. ج. 65 ع. 2: 101–12. DOI:10.1111/j.0009-9163.2004.00198.x. PMID:14984468. S2CID:34964226.
Popovic، M؛ Goobie, S؛ Morrison, J؛ Ellis, L؛ Ehtesham, N؛ Richards, N؛ Boocock, G؛ Durie, PR؛ Rommens, JM (أبريل 2002). "Fine mapping of the locus for Shwachman-Diamond syndrome at 7q11, identification of shared disease haplotypes, and exclusion of TPST1 as a candidate gene". European Journal of Human Genetics. ج. 10 ع. 4: 250–8. DOI:10.1038/sj.ejhg.5200798. PMID:12032733. S2CID:12667823.

web.archive.org

Orkin، Stuart H.؛ Nathan، David G.؛ Ginsburg، David؛ A. Thomas Look (2009). Nathan and Oski's hematology of infancy and childhood. Elsevier Health Sciences. ص. 344–. ISBN:978-1-4160-3430-8. مؤرشف من الأصل في 2021-10-05. اطلع عليه بتاريخ 2011-08-08.