Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

84 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Genetic studies in neural tube defects. NTD Collaborative Group.
Melvin EC, George TM, Worley G, Franklin A, Mackey J, Viles K, Shah N, Drake CR, Enterline DS, McLone D, Nye J, Oakes WJ, McLaughlin C, Walker ML, Peterson P, Brei T, Buran C, Aben J, Ohm B, Bermans I, Qumsiyeh M, Vance J, Pericak-Vance MA, Speer MC. Melvin EC, et al. Among authors: qumsiyeh m. Pediatr Neurosurg. 2000 Jan;32(1):1-9. doi: 10.1159/000028889. Pediatr Neurosurg. 2000. PMID: 10765131 Review.
Genetic studies of autistic disorder and chromosome 7.
Ashley-Koch A, Wolpert CM, Menold MM, Zaeem L, Basu S, Donnelly SL, Ravan SA, Powell CM, Qumsiyeh MB, Aylsworth AS, Vance JM, Gilbert JR, Wright HH, Abramson RK, DeLong GR, Cuccaro ML, Pericak-Vance MA. Ashley-Koch A, et al. Among authors: qumsiyeh mb. Genomics. 1999 Nov 1;61(3):227-36. doi: 10.1006/geno.1999.5968. Genomics. 1999. PMID: 10552924
Three probands with autistic disorder and isodicentric chromosome 15.
Wolpert CM, Menold MM, Bass MP, Qumsiyeh MB, Donnelly SL, Ravan SA, Vance JM, Gilbert JR, Abramson RK, Wright HH, Cuccaro ML, Pericak-Vance MA. Wolpert CM, et al. Among authors: qumsiyeh mb. Am J Med Genet. 2000 Jun 12;96(3):365-72. doi: 10.1002/1096-8628(20000612)96:3<365::aid-ajmg25>3.0.co;2-x. Am J Med Genet. 2000. PMID: 10898916 Review.
Postnatal developmental delay and chromosomal abnormalities.
Ahmed MN, DeLong GR, Qumsiyeh MB. Ahmed MN, et al. Among authors: qumsiyeh mb. Clin Pediatr (Phila). 2000 Apr;39(4):233-5. doi: 10.1177/000992280003900407. Clin Pediatr (Phila). 2000. PMID: 10791136 No abstract available.
Familial subepithelial corneal amyloidosis (gelatinous drop-like corneal dystrophy): exclusion of linkage to lactoferrin gene.
Klintworth GK, Sommer JR, Obrian G, Han L, Ahmed MN, Qumsiyeh MB, Lin PY, Basti S, Reddy MK, Kanai A, Hotta Y, Sugar J, Kumaramanickavel G, Munier F, Schorderet DF, El Matri L, Iwata F, Kaiser-Kupfer M, Nagata M, Nakayasu K, Hejtmancik JF, Teng CT. Klintworth GK, et al. Among authors: qumsiyeh mb. Mol Vis. 1998 Dec 31;4:31. Mol Vis. 1998. PMID: 9873069 Free article.
84 results