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Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1981 | 1 |
1983 | 1 |
1994 | 1 |
1995 | 1 |
2001 | 2 |
2005 | 1 |
2023 | 0 |
Search Results
7
results
Results by year
Page 1
Retinoblastoma and the 13q deletion syndrome.
J Pediatr Ophthalmol Strabismus. 2001 Jul-Aug;38(4):247-50. doi: 10.3928/0191-3913-20010701-14.
J Pediatr Ophthalmol Strabismus. 2001.
PMID: 11495315
No abstract available.
Isolated congenital atrichia in an Omani kindred.
Kenue RK, al-Dhafri KS.
Kenue RK, et al.
Dermatology. 1994;188(1):72-5. doi: 10.1159/000247092.
Dermatology. 1994.
PMID: 8305765
Item in Clipboard
Cytogenetic analysis of children suspected of chromosomal abnormalities.
Kenue RK, Raj AK, Harris PF, el-Bualy MS.
Kenue RK, et al.
J Trop Pediatr. 1995 Apr;41(2):77-80. doi: 10.1093/tropej/41.2.77.
J Trop Pediatr. 1995.
PMID: 7776401
Item in Clipboard
Acardia syndrome coexisting with gastroschisis in the co-twin.
Habbal OA, Kenue RK, Venugopalan P.
Habbal OA, et al. Among authors: kenue rk.
Clin Dysmorphol. 2005 Jan;14(1):45-47.
Clin Dysmorphol. 2005.
PMID: 15602095
Item in Clipboard
Ring chromosome 13 in an Omani infant boy with mental retardation and multiple congenital anomalies.
Venugopalan P, Kenue RK.
Venugopalan P, et al. Among authors: kenue rk.
Saudi Med J. 2001 Sep;22(9):800-3.
Saudi Med J. 2001.
PMID: 11590457
Item in Clipboard
H-Y antigen and karyotypic analysis in patients with abnormal sexual differentiation and development.
Kucheria K, Kenue RK, Mitra DK, Bhargava V, Taneja N, UpadhyayaP.
Kucheria K, et al. Among authors: kenue rk.
Indian Pediatr. 1983 Aug;20(8):593-7.
Indian Pediatr. 1983.
PMID: 6662584
No abstract available.
Item in Clipboard
An Indian family with postaxial polydactyly in four generations.
Kucheria K, Kenue RK, Taneja N.
Kucheria K, et al. Among authors: kenue rk.
Clin Genet. 1981 Jul;20(1):36-9. doi: 10.1111/j.1399-0004.1981.tb01803.x.
Clin Genet. 1981.
PMID: 7296946
Item in Clipboard
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