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Publications by Mr I K Jalili |
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A progressive cone-rod dystrophy and
amelogenesis imperfecta: a new syndrome.
(OMIM 217080)
Jalili IK, Smith
NJD.
Journal of Medical Genetics,
l988;25:738-740.
(Reprint) |
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A
syndrome of amelogenesis imperfecta associated with cone-rod dystrophy: dental
and ophthalmic findings - abstract.
Jalili IK, Smith NJD. Journal of Dental Research 1988.
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Cone
rod congenital amaurosis associated with
congenital hypertrichosis: an
autosomal recessive condition.
Jalili
IK. Journal
of Medical Genetics, l989;26:504-5l0.
(Reprint)
-
(OMIM
204110) |
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The
above two conditions were also included in the London Dysmorphology Database of Winter
and Baraitser, and registered as Syndromes #4615 and #4740 respectively by The
Murdoch Institute for Research into Birth Defects Limited, Royal Children's
Hospital, Flemington Road, Parkville 3052, Melbourne, Australia.
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Increased band sharing in DNA fingerprints of an
inbred human population. Bellamy RJ, Inglehearn CF, Jalili IK,
Jeffreys AJ, Bhattacharya SS. Human Genetics 1991;87:341-347.
(Request
Reprint)
The paper have demonstrated that moderate but
prolonged inbreeding can lead to increased similarity in human DNA
fingerprints. This should be considered when analysing DNA fingerprints in
forensic or paternity cases involving members of an inbred community. |
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Congenital
onset central chorioretinal dystrophy associated with high myopia:
Iqbal M,
Jalili IK.
Eye
1998;12:260-265. (Request
a reprint) |
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Ophthalmic Primary Care:
The
Warrington
Model.
Peckar
CO, Wishart MS, Jalili IK, Mathews P. European
J of Implant and Refractive Surgery 1994:6:1:2-5.
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E coli panophthalmitis
with orbital cellulitis.
Burns SJ, Scott JA, Hiscott PS, Hebbar G, Kamauddin J,
Jalili IK.
Eye. 1997;11 (
Pt 3):436-8. |
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Identification of a locus on chromosome 2q11 at which recessive amelogenesis imperfecta and cone-rod dystrophy cosegregate.
Downey LM,
Keen TJ, Jalili IK, McHale J, Aldred MJ, Robertson SP, Mighell A, Fayle S,
Wissinger B, Inglehearn CF. European
Journal of Human Genetics 2002:19,865-860. |
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Jalili Syndrome - Cone-Rod Dystrophy
(CRD) and Amelogenesis Imperfecta (AI); Six Families and Consistent Linkage to
2q11.
ARVO Presentation
Inglehearn CF, El-Sayed W, Shore RC,
Jalili IK, Dollfus H, Carlos R,
Blain KM, Mansfield DC, Moore AT,
Mighell AJ. (The Association for Research in Vision and
Ophthalmology (ARVO)
2008. |
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Jalili Syndrome - Cone-Rod Dystrophy
(CRD) and Amelogenesis Imperfecta (AI); Six Families and Consistent Linkage to
2q11.
Inglehearn
CF, El-Sayed W, Shore RC,
Jalili IK, Dollfus H, Carlos R,
Blain KM, Mansfield DC, Moore AT,
Mighell AJ.
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Amelogenesis
Imperfecta and Central Blindness: An Inherited Syndrome.
Mighell
AJ, El-Sayed W, Shore RC,
Jalili IK, Dollfus H, Bloch-Zupan A,
Carlos R, Blain K, Mansfield D,
Moore AT and Inglehearn CF.
International Association for Dental
research (IADR), July 2008.
Link to the article |
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Synopses
on post-traumatic headache (PTH) and related topics: a review. Electronic
publication.
Jalili IK.
(Reprint) |
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Mutations in CNNM4 Cause Jalili Syndrome, Consisting
of Autosomal-Recessive Cone-Rod Dystrophy and Amelogenesis Imperfecta
(Link to the article)
Parry DA, Mighell
AJ, El-Sayed W, Shore RC,
Jalili IK, Dollfus H, Bloch-Zupan A,
Carlos R, Carr IM, Downey LM, Blain KM, Mansfield DC, Shahrabi M,
Heidari M, Aref P, Abbasi M, Michaelides M, Moore AT, Kirkham J, Inglehearn CF.
American Journal of Human Genetics; 2009:84:266–273.
The gene was found simultaneously by Polok and
Colleagues. See American Journal of Human genetics. 2009,84:259-65. |
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Refer also to the section on presentation. |
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Other |
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For other research
click on this link |
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