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Craniofacial dyssynostosis with cryptorchidism and normal stature.
Am J Med Genet. 1998 Aug 27;79(1):5-7. doi: 10.1002/(sici)1096-8628(19980827)79:1<5::aid-ajmg2>3.0.co;2-p.
Am J Med Genet. 1998.
PMID: 9738859
Unusual traits associated with Robinow syndrome.
Sabry MA, Ismail EA, al-Naggar RL, al-Torki NA, Farah S, al-Awadi SA, Obenbergerova D, Bastaki L.
Sabry MA, et al. Among authors: al torki na.
J Med Genet. 1997 Sep;34(9):736-40. doi: 10.1136/jmg.34.9.736.
J Med Genet. 1997.
PMID: 9321759
Free PMC article.
Item in Clipboard
Kenny-Caffey syndrome: an Arab variant?
Sabry MA, Farag TI, Shaltout AA, Zaki M, Al-Mazidi Z, Abulhassan SJ, Al-Torki N, Quishawi A, Al Awadi SA.
Sabry MA, et al.
Clin Genet. 1999 Jan;55(1):44-9. doi: 10.1034/j.1399-0004.1999.550108.x.
Clin Genet. 1999.
PMID: 10066031
Review.
Item in Clipboard
Gerodermia osteodysplastica in a Bedouin sibship: further delineation of the syndrome.
al-Torki NA, al-Awadi SA, Cindro-Heberie L, Sabry MA.
al-Torki NA, et al.
Clin Dysmorphol. 1997 Jan;6(1):51-5.
Clin Dysmorphol. 1997.
PMID: 9018419
Item in Clipboard
Lowry-Maclean syndrome with osteopenic bones and possible autosomal dominant inheritance in a Bedouin family.
Al-Torki NA, Sabry MA, Al-Awadi SA, Al-Tarkeit N.
Al-Torki NA, et al.
Am J Med Genet. 1997 Dec 31;73(4):491-2. doi: 10.1002/(sici)1096-8628(19971231)73:4<491::aid-ajmg23>3.0.co;2-l.
Am J Med Genet. 1997.
PMID: 9415481
No abstract available.
Item in Clipboard
Additional EFNB1 mutations in craniofrontonasal syndrome.
Wallis D, Lacbawan F, Jain M, Der Kaloustian VM, Steiner CE, Moeschler JB, Losken HW, Kaitila II, Cantrell S, Proud VK, Carey JC, Day DW, Lev D, Teebi AS, Robinson LK, Hoyme HE, Al-Torki N, Siegel-Bartelt J, Mulliken JB, Robin NH, Saavedra D, Zackai EH, Muenke M.
Wallis D, et al.
Am J Med Genet A. 2008 Aug 1;146A(15):2008-12. doi: 10.1002/ajmg.a.32388.
Am J Med Genet A. 2008.
PMID: 18627045
Free PMC article.
No abstract available.
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