ALX4 (Arabic Wikipedia)

Analysis of information sources in references of the Wikipedia article "ALX4" in Arabic language version.

Last modified: 11:03:00, 20 January 2026 (UTC)

Ref.Un. Ref.Website

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1812nih.gov

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85doi.org

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32web.archive.org

1^st place

21biologists.org

5,151^st place

3,629^th place

11archive.org

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archive.org (Global: 6^th place; Arabic: 3^rd place)

Wu YQ، Badano JL، McCaskill C، Vogel H، Potocki L، Shaffer LG (نوفمبر 2000). "Haploinsufficiency of ALX4 as a potential cause of parietal foramina in the 11p11.2 contiguous gene-deletion syndrome". American Journal of Human Genetics. ج. 67 ع. 5: 1327–32. DOI:10.1016/S0002-9297(07)62963-2. PMC:1288575. PMID:11017806.

biologists.org (Global: 5,151^st place; Arabic: 3,629^th place)

dev.biologists.org

Takahashi M، Tamura K، Büscher D، Masuya H، Yonei-Tamura S، Matsumoto K، Naitoh-Matsuo M، Takeuchi J، Ogura K، Shiroishi T، Ogura T، Izpisúa Belmonte JC (نوفمبر 1998). "The role of Alx-4 in the establishment of anteroposterior polarity during vertebrate limb development". Development. ج. 125 ع. 22: 4417–25. PMID:9778501. مؤرشف من الأصل في 2018-06-17.

doi.org (Global: 2^nd place; Arabic: 4^th place)

Forsthoefel PF (نوفمبر 1963). "The embryological development of the effects of Strong's luxoid gene in the mouse". Journal of Morphology. ج. 113 ع. 3: 427–51. DOI:10.1002/jmor.1051130307. PMID:14079603.
Kuijper S، Feitsma H، Sheth R، Korving J، Reijnen M، Meijlink F (سبتمبر 2005). "Function and regulation of Alx4 in limb development: complex genetic interactions with Gli3 and Shh". Developmental Biology. ج. 285 ع. 2: 533–44. DOI:10.1016/j.ydbio.2005.06.017. PMID:16039644.
Panman L، Drenth T، Tewelscher P، Zuniga A، Zeller R (1 يوليو 2004). "Genetic interaction of Gli3 and Alx4 during limb development". The International Journal of Developmental Biology. ج. 49 ع. 4: 443–8. DOI:10.1387/ijdb.051984lp. PMID:15968591.
Kayserili H، Uz E، Niessen C، Vargel I، Alanay Y، Tuncbilek G، Yigit G، Uyguner O، Candan S، Okur H، Kaygin S، Balci S، Mavili E، Alikasifoglu M، Haase I، Wollnik B، Akarsu NA (نوفمبر 2009). "ALX4 dysfunction disrupts craniofacial and epidermal development". Human Molecular Genetics. ج. 18 ع. 22: 4357–66. DOI:10.1093/hmg/ddp391. PMID:19692347.
Wu YQ، Badano JL، McCaskill C، Vogel H، Potocki L، Shaffer LG (نوفمبر 2000). "Haploinsufficiency of ALX4 as a potential cause of parietal foramina in the 11p11.2 contiguous gene-deletion syndrome". American Journal of Human Genetics. ج. 67 ع. 5: 1327–32. DOI:10.1016/S0002-9297(07)62963-2. PMC:1288575. PMID:11017806.

nih.gov (Global: 5^th place; Arabic: 6^th place)

pubmed.ncbi.nlm.nih.gov

Forsthoefel PF (نوفمبر 1963). "The embryological development of the effects of Strong's luxoid gene in the mouse". Journal of Morphology. ج. 113 ع. 3: 427–51. DOI:10.1002/jmor.1051130307. PMID:14079603.
Kuijper S، Feitsma H، Sheth R، Korving J، Reijnen M، Meijlink F (سبتمبر 2005). "Function and regulation of Alx4 in limb development: complex genetic interactions with Gli3 and Shh". Developmental Biology. ج. 285 ع. 2: 533–44. DOI:10.1016/j.ydbio.2005.06.017. PMID:16039644.
Niswander L (2002). "Interplay between the molecular signals that control vertebrate limb development". The International Journal of Developmental Biology. ج. 46 ع. 7: 877–81. PMID:12455624.
Panman L، Drenth T، Tewelscher P، Zuniga A، Zeller R (1 يوليو 2004). "Genetic interaction of Gli3 and Alx4 during limb development". The International Journal of Developmental Biology. ج. 49 ع. 4: 443–8. DOI:10.1387/ijdb.051984lp. PMID:15968591.
Takahashi M، Tamura K، Büscher D، Masuya H، Yonei-Tamura S، Matsumoto K، Naitoh-Matsuo M، Takeuchi J، Ogura K، Shiroishi T، Ogura T، Izpisúa Belmonte JC (نوفمبر 1998). "The role of Alx-4 in the establishment of anteroposterior polarity during vertebrate limb development". Development. ج. 125 ع. 22: 4417–25. PMID:9778501. مؤرشف من الأصل في 2018-06-17.
Meijlink F، Beverdam A، Brouwer A، Oosterveen TC، Berge DT (1999). "Vertebrate aristaless-related genes". The International Journal of Developmental Biology. ج. 43 ع. 7: 651–63. PMID:10668975.
Kayserili H، Uz E، Niessen C، Vargel I، Alanay Y، Tuncbilek G، Yigit G، Uyguner O، Candan S، Okur H، Kaygin S، Balci S، Mavili E، Alikasifoglu M، Haase I، Wollnik B، Akarsu NA (نوفمبر 2009). "ALX4 dysfunction disrupts craniofacial and epidermal development". Human Molecular Genetics. ج. 18 ع. 22: 4357–66. DOI:10.1093/hmg/ddp391. PMID:19692347.
Wu YQ، Badano JL، McCaskill C، Vogel H، Potocki L، Shaffer LG (نوفمبر 2000). "Haploinsufficiency of ALX4 as a potential cause of parietal foramina in the 11p11.2 contiguous gene-deletion syndrome". American Journal of Human Genetics. ج. 67 ع. 5: 1327–32. DOI:10.1016/S0002-9297(07)62963-2. PMC:1288575. PMID:11017806.
Bartsch O، Wuyts W، Van Hul W، Hecht JT، Meinecke P، Hogue D، Werner W، Zabel B، Hinkel GK، Powell CM، Shaffer LG، Willems PJ (أبريل 1996). "Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm of chromosome 11". American Journal of Human Genetics. ج. 58 ع. 4: 734–42. PMC:1914683. PMID:8644736.

ncbi.nlm.nih.gov

"Entrez Gene: ALX4 aristaless-like homeobox 4". مؤرشف من الأصل في 2010-12-05.
Wu YQ، Badano JL، McCaskill C، Vogel H، Potocki L، Shaffer LG (نوفمبر 2000). "Haploinsufficiency of ALX4 as a potential cause of parietal foramina in the 11p11.2 contiguous gene-deletion syndrome". American Journal of Human Genetics. ج. 67 ع. 5: 1327–32. DOI:10.1016/S0002-9297(07)62963-2. PMC:1288575. PMID:11017806.
Bartsch O، Wuyts W، Van Hul W، Hecht JT، Meinecke P، Hogue D، Werner W، Zabel B، Hinkel GK، Powell CM، Shaffer LG، Willems PJ (أبريل 1996). "Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm of chromosome 11". American Journal of Human Genetics. ج. 58 ع. 4: 734–42. PMC:1914683. PMID:8644736.

web.archive.org (Global: 1^st place; Arabic: 1^st place)

Takahashi M، Tamura K، Büscher D، Masuya H، Yonei-Tamura S، Matsumoto K، Naitoh-Matsuo M، Takeuchi J، Ogura K، Shiroishi T، Ogura T، Izpisúa Belmonte JC (نوفمبر 1998). "The role of Alx-4 in the establishment of anteroposterior polarity during vertebrate limb development". Development. ج. 125 ع. 22: 4417–25. PMID:9778501. مؤرشف من الأصل في 2018-06-17.
"Entrez Gene: ALX4 aristaless-like homeobox 4". مؤرشف من الأصل في 2010-12-05.

ALX4 (Arabic Wikipedia)

archive.org (Global: 6th place; Arabic: 3rd place)

biologists.org (Global: 5,151st place; Arabic: 3,629th place)