تغاير الزيجوت المركب (Arabic Wikipedia)

Analysis of information sources in references of the Wikipedia article "تغاير الزيجوت المركب" in Arabic language version.

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9nih.gov

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5doi.org

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2web.archive.org

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2archive.org

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1uq.edu.au

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archive.org

Rossi E، Olynyk JK، Cullen DJ، Papadopoulos G، Bulsara M، Summerville L، Powell LW (فبراير 2000). "Compound heterozygous hemochromatosis genotype predicts increased iron and erythrocyte indices in women". Clinical Chemistry. ج. 46 ع. 2: 162–166. PMID:10657371.
Anderson JA، Fisch R، Miller E، Doeden D (مارس 1966). "Atypical phenylketonuric heterozygote. Deficiency in phenylalanine hydroxylase and transaminase activity". Journal of Pediatrics. ج. 68 ع. 3: 351–360. DOI:10.1016/s0022-3476(66)80237-8. PMID:4379218.

doi.org

KJ Allen؛ LC Gurrin؛ CC Constantine؛ وآخرون (17 يناير 2008). "Iron-Overload–Related Disease in HFE Hereditary Hemochromatosis" (PDF). New England Journal of Medicine. ج. 358 ع. 3: 221–230. DOI:10.1056/NEJMoa073286. PMID:18199861. مؤرشف من الأصل (PDF) في 2023-04-07.
Deugnier Y، Mosser J (أغسطس 2008). "Modifying factors of the HFE hemochromatosis phenotype". Expert Review of Gastroenterology & Hepatology. ج. 2 ع. 4: 531–540. DOI:10.1586/17474124.2.4.531. PMID:19072401.
Anderson JA، Fisch R، Miller E، Doeden D (مارس 1966). "Atypical phenylketonuric heterozygote. Deficiency in phenylalanine hydroxylase and transaminase activity". Journal of Pediatrics. ج. 68 ع. 3: 351–360. DOI:10.1016/s0022-3476(66)80237-8. PMID:4379218.
Gonzalez-Redondo JM، Stoming TA، Lanclos KD، وآخرون (1988). "Clinical and genetic heterogeneity in black patients with homozygous beta-thalassemia from the southeastern United States". Blood. ج. 72 ع. 3: 1007–1014. DOI:10.1182/blood.V72.3.1007.bloodjournal7231007. PMID:2458145.
Witkowska HE؛ Lubin BH؛ Beuzard Y؛ Baruchel S؛ Esseltine DW؛ Vichinsky EP؛ Kleman KM؛ Bardakdjian-Michau J؛ Pinkoski L؛ Cahn S؛ وآخرون (17 أكتوبر 1991). "Sickle cell disease in a patient with sickle cell trait and compound heterozygosity for hemoglobin S and hemoglobin Quebec-Chori". New England Journal of Medicine. Massachusetts Medical Society. ج. 325 ع. 16: 1150–1154. DOI:10.1056/NEJM199110173251607. PMID:1891024.

jbc.org

Ohno, Kousaku & Suzuki, Kunihiko (5 ديسمبر 1988). "Multiple Abnormal beta-Hexosaminidase alpha-Chain mRNAs in a Compound-Heterozygous Ashkenazi Jewish Patient with Tay–Sachs Disease" (PDF). Journal of Biological Chemistry. ج. 263 ع. 34: 18563–7. PMID:2973464. مؤرشف من الأصل (PDF) في 2007-09-26. اطلع عليه بتاريخ 2007-05-11.

nih.gov

pubmed.ncbi.nlm.nih.gov

KJ Allen؛ LC Gurrin؛ CC Constantine؛ وآخرون (17 يناير 2008). "Iron-Overload–Related Disease in HFE Hereditary Hemochromatosis" (PDF). New England Journal of Medicine. ج. 358 ع. 3: 221–230. DOI:10.1056/NEJMoa073286. PMID:18199861. مؤرشف من الأصل (PDF) في 2023-04-07.
Rossi E، Olynyk JK، Cullen DJ، Papadopoulos G، Bulsara M، Summerville L، Powell LW (فبراير 2000). "Compound heterozygous hemochromatosis genotype predicts increased iron and erythrocyte indices in women". Clinical Chemistry. ج. 46 ع. 2: 162–166. PMID:10657371.
Deugnier Y، Mosser J (أغسطس 2008). "Modifying factors of the HFE hemochromatosis phenotype". Expert Review of Gastroenterology & Hepatology. ج. 2 ع. 4: 531–540. DOI:10.1586/17474124.2.4.531. PMID:19072401.
Anderson JA، Fisch R، Miller E، Doeden D (مارس 1966). "Atypical phenylketonuric heterozygote. Deficiency in phenylalanine hydroxylase and transaminase activity". Journal of Pediatrics. ج. 68 ع. 3: 351–360. DOI:10.1016/s0022-3476(66)80237-8. PMID:4379218.
Avigad S، Kleiman S، Weinstein M، Cohen BE، Schwartz G، Woo SL، Shiloh Y (أغسطس 1991). "Compound heterozygosity in nonphenylketonuria hyperphenylalanemia: The contribution of mutations for classical phenylketonuria". American Journal of Human Genetics. ج. 49 ع. 2: 393–399. PMC:1683284. PMID:1867197.
Ohno, Kousaku & Suzuki, Kunihiko (5 ديسمبر 1988). "Multiple Abnormal beta-Hexosaminidase alpha-Chain mRNAs in a Compound-Heterozygous Ashkenazi Jewish Patient with Tay–Sachs Disease" (PDF). Journal of Biological Chemistry. ج. 263 ع. 34: 18563–7. PMID:2973464. مؤرشف من الأصل (PDF) في 2007-09-26. اطلع عليه بتاريخ 2007-05-11.
Gonzalez-Redondo JM، Stoming TA، Lanclos KD، وآخرون (1988). "Clinical and genetic heterogeneity in black patients with homozygous beta-thalassemia from the southeastern United States". Blood. ج. 72 ع. 3: 1007–1014. DOI:10.1182/blood.V72.3.1007.bloodjournal7231007. PMID:2458145.
Witkowska HE؛ Lubin BH؛ Beuzard Y؛ Baruchel S؛ Esseltine DW؛ Vichinsky EP؛ Kleman KM؛ Bardakdjian-Michau J؛ Pinkoski L؛ Cahn S؛ وآخرون (17 أكتوبر 1991). "Sickle cell disease in a patient with sickle cell trait and compound heterozygosity for hemoglobin S and hemoglobin Quebec-Chori". New England Journal of Medicine. Massachusetts Medical Society. ج. 325 ع. 16: 1150–1154. DOI:10.1056/NEJM199110173251607. PMID:1891024.

ncbi.nlm.nih.gov

Avigad S، Kleiman S، Weinstein M، Cohen BE، Schwartz G، Woo SL، Shiloh Y (أغسطس 1991). "Compound heterozygosity in nonphenylketonuria hyperphenylalanemia: The contribution of mutations for classical phenylketonuria". American Journal of Human Genetics. ج. 49 ع. 2: 393–399. PMC:1683284. PMID:1867197.

uq.edu.au

espace.library.uq.edu.au

KJ Allen؛ LC Gurrin؛ CC Constantine؛ وآخرون (17 يناير 2008). "Iron-Overload–Related Disease in HFE Hereditary Hemochromatosis" (PDF). New England Journal of Medicine. ج. 358 ع. 3: 221–230. DOI:10.1056/NEJMoa073286. PMID:18199861. مؤرشف من الأصل (PDF) في 2023-04-07.

web.archive.org

KJ Allen؛ LC Gurrin؛ CC Constantine؛ وآخرون (17 يناير 2008). "Iron-Overload–Related Disease in HFE Hereditary Hemochromatosis" (PDF). New England Journal of Medicine. ج. 358 ع. 3: 221–230. DOI:10.1056/NEJMoa073286. PMID:18199861. مؤرشف من الأصل (PDF) في 2023-04-07.
Ohno, Kousaku & Suzuki, Kunihiko (5 ديسمبر 1988). "Multiple Abnormal beta-Hexosaminidase alpha-Chain mRNAs in a Compound-Heterozygous Ashkenazi Jewish Patient with Tay–Sachs Disease" (PDF). Journal of Biological Chemistry. ج. 263 ع. 34: 18563–7. PMID:2973464. مؤرشف من الأصل (PDF) في 2007-09-26. اطلع عليه بتاريخ 2007-05-11.