Jalili syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Jalili syndrome" in English language version.

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Jalili, I K; Smith, N J (1988). "A progressive cone-rod dystrophy and amelogenesis imperfecta: A new syndrome". Journal of Medical Genetics. 25 (11): 738–40. doi:10.1136/jmg.25.11.738. PMC 1051576. PMID 3236352.
Michaelides, M; Bloch-Zupan, A; Holder, GE; Hunt, DM; Moore, AT (2004). "An autosomal recessive cone-rod dystrophy associated with amelogenesis imperfecta". Journal of Medical Genetics. 41 (6): 468–73. doi:10.1136/jmg.2003.015792. PMC 1735797. PMID 15173235.
Polok, Bozena; Escher, Pascal; Ambresin, Aude; Chouery, Eliane; Bolay, Sylvain; Meunier, Isabelle; Nan, Francis; Hamel, Christian; Munier, Francis L. (2009). "Mutations in CNNM4 Cause Recessive Cone-Rod Dystrophy with Amelogenesis Imperfecta". The American Journal of Human Genetics. 84 (2): 259–65. doi:10.1016/j.ajhg.2009.01.006. PMC 2668018. PMID 19200527.
Parry, David A.; Mighell, Alan J.; El-Sayed, Walid; Shore, Roger C.; Jalili, Ismail K.; Dollfus, Hélène; Bloch-Zupan, Agnes; Carlos, Roman; Carr, Ian M. (2009). "Mutations in CNNM4 Cause Jalili Syndrome, Consisting of Autosomal-Recessive Cone-Rod Dystrophy and Amelogenesis Imperfecta". The American Journal of Human Genetics. 84 (2): 266–73. doi:10.1016/j.ajhg.2009.01.009. PMC 2668026. PMID 19200525.

Jalili, I K; Smith, N J (1988). "A progressive cone-rod dystrophy and amelogenesis imperfecta: A new syndrome". Journal of Medical Genetics. 25 (11): 738–40. doi:10.1136/jmg.25.11.738. PMC 1051576. PMID 3236352.
Michaelides, M; Bloch-Zupan, A; Holder, GE; Hunt, DM; Moore, AT (2004). "An autosomal recessive cone-rod dystrophy associated with amelogenesis imperfecta". Journal of Medical Genetics. 41 (6): 468–73. doi:10.1136/jmg.2003.015792. PMC 1735797. PMID 15173235.
Polok, Bozena; Escher, Pascal; Ambresin, Aude; Chouery, Eliane; Bolay, Sylvain; Meunier, Isabelle; Nan, Francis; Hamel, Christian; Munier, Francis L. (2009). "Mutations in CNNM4 Cause Recessive Cone-Rod Dystrophy with Amelogenesis Imperfecta". The American Journal of Human Genetics. 84 (2): 259–65. doi:10.1016/j.ajhg.2009.01.006. PMC 2668018. PMID 19200527.
Parry, David A.; Mighell, Alan J.; El-Sayed, Walid; Shore, Roger C.; Jalili, Ismail K.; Dollfus, Hélène; Bloch-Zupan, Agnes; Carlos, Roman; Carr, Ian M. (2009). "Mutations in CNNM4 Cause Jalili Syndrome, Consisting of Autosomal-Recessive Cone-Rod Dystrophy and Amelogenesis Imperfecta". The American Journal of Human Genetics. 84 (2): 266–73. doi:10.1016/j.ajhg.2009.01.009. PMC 2668026. PMID 19200525.

Jalili, I K; Smith, N J (1988). "A progressive cone-rod dystrophy and amelogenesis imperfecta: A new syndrome". Journal of Medical Genetics. 25 (11): 738–40. doi:10.1136/jmg.25.11.738. PMC 1051576. PMID 3236352.
Michaelides, M; Bloch-Zupan, A; Holder, GE; Hunt, DM; Moore, AT (2004). "An autosomal recessive cone-rod dystrophy associated with amelogenesis imperfecta". Journal of Medical Genetics. 41 (6): 468–73. doi:10.1136/jmg.2003.015792. PMC 1735797. PMID 15173235.
Polok, Bozena; Escher, Pascal; Ambresin, Aude; Chouery, Eliane; Bolay, Sylvain; Meunier, Isabelle; Nan, Francis; Hamel, Christian; Munier, Francis L. (2009). "Mutations in CNNM4 Cause Recessive Cone-Rod Dystrophy with Amelogenesis Imperfecta". The American Journal of Human Genetics. 84 (2): 259–65. doi:10.1016/j.ajhg.2009.01.006. PMC 2668018. PMID 19200527.
Parry, David A.; Mighell, Alan J.; El-Sayed, Walid; Shore, Roger C.; Jalili, Ismail K.; Dollfus, Hélène; Bloch-Zupan, Agnes; Carlos, Roman; Carr, Ian M. (2009). "Mutations in CNNM4 Cause Jalili Syndrome, Consisting of Autosomal-Recessive Cone-Rod Dystrophy and Amelogenesis Imperfecta". The American Journal of Human Genetics. 84 (2): 266–73. doi:10.1016/j.ajhg.2009.01.009. PMC 2668026. PMID 19200525.