Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

86 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Macrocephaly with multiple lipomas and hemangiomas.
Zonana J, Rimoin DL, Davis DC. Zonana J, et al. J Pediatr. 1976 Oct;89(4):600-3. doi: 10.1016/s0022-3476(76)80397-6. J Pediatr. 1976. PMID: 957004 No abstract available.
Macrocephaly with hamartomas: Bannayan-Zonana syndrome.
Miles JH, Zonana J, Mcfarlane J, Aleck KA, Bawle E. Miles JH, et al. Among authors: zonana j. Am J Med Genet. 1984 Oct;19(2):225-34. doi: 10.1002/ajmg.1320190204. Am J Med Genet. 1984. PMID: 6507473
The Bannayan-Zonana syndrome is an autosomal-dominant trait with male predominance of affected individuals....
The Bannayan-Zonana syndrome is an autosomal-dominant trait with male predominance of affected individuals....
Coloboma, congenital heart disease, and choanal atresia with multiple anomalies: CHARGE association.
Pagon RA, Graham JM Jr, Zonana J, Yong SL. Pagon RA, et al. Among authors: zonana j. J Pediatr. 1981 Aug;99(2):223-7. doi: 10.1016/s0022-3476(81)80454-4. J Pediatr. 1981. PMID: 6166737
Heterogeneity of nonlethal severe short-limbed dwarfism.
Romeo G, Zonana J, Rimoin DL, Lachman RS, Scott CI Jr, Kaveggia EG, Spranger JW, Opitz JM. Romeo G, et al. Among authors: zonana j. J Pediatr. 1977 Dec;91(6):918-23. doi: 10.1016/s0022-3476(77)80890-1. J Pediatr. 1977. PMID: 925797
Dominant inheritance of cerebral gigantism.
Zonana J, Sotos JF, Romshe CA, Fisher DA, Elders MJ, Rimoin DL. Zonana J, et al. J Pediatr. 1977 Aug;91(2):251-6. doi: 10.1016/s0022-3476(77)80822-6. J Pediatr. 1977. PMID: 889595
CHARGE association.
Pagon RA, Zonana J, Graham JM. Pagon RA, et al. Among authors: zonana j. Pediatrics. 1982 Nov;70(5):827-8. Pediatrics. 1982. PMID: 7133839 No abstract available.
Improved definition of carrier status in X-linked hypohidrotic ectodermal dysplasia by use of restriction fragment length polymorphism-based linkage analysis.
Zonana J, Sarfarazi M, Thomas NS, Clarke A, Marymee K, Harper PS. Zonana J, et al. J Pediatr. 1989 Mar;114(3):392-9. doi: 10.1016/s0022-3476(89)80556-6. J Pediatr. 1989. PMID: 2564048
Further clinical and molecular delineation of the 15q24 microdeletion syndrome.
Mefford HC, Rosenfeld JA, Shur N, Slavotinek AM, Cox VA, Hennekam RC, Firth HV, Willatt L, Wheeler P, Morrow EM, Cook J, Sullivan R, Oh A, McDonald MT, Zonana J, Keller K, Hannibal MC, Ball S, Kussmann J, Gorski J, Zelewski S, Banks V, Smith W, Smith R, Paull L, Rosenbaum KN, Amor DJ, Silva J, Lamb A, Eichler EE. Mefford HC, et al. Among authors: zonana j. J Med Genet. 2012 Feb;49(2):110-8. doi: 10.1136/jmedgenet-2011-100499. Epub 2011 Dec 17. J Med Genet. 2012. PMID: 22180641 Free PMC article.
Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome.
Driscoll DA, Spinner NB, Budarf ML, McDonald-McGinn DM, Zackai EH, Goldberg RB, Shprintzen RJ, Saal HM, Zonana J, Jones MC, et al. Driscoll DA, et al. Among authors: zonana j. Am J Med Genet. 1992 Sep 15;44(2):261-8. doi: 10.1002/ajmg.1320440237. Am J Med Genet. 1992. PMID: 1360769
Comparison of the 15q deletions in Prader-Willi and Angelman syndromes: specific regions, extent of deletions, parental origin, and clinical consequences.
Magenis RE, Toth-Fejel S, Allen LJ, Black M, Brown MG, Budden S, Cohen R, Friedman JM, Kalousek D, Zonana J, et al. Magenis RE, et al. Among authors: zonana j. Am J Med Genet. 1990 Mar;35(3):333-49. doi: 10.1002/ajmg.1320350307. Am J Med Genet. 1990. PMID: 2309780
86 results
Jump to page
Feedback