Pages that link to "Q33248334"

The following pages link to Isolation and regional localization of 35 unique anonymous DNA markers for human chromosome 22. (Q33248334):

Displaying 22 items.

• Isolation and Characterization of a Gene from the DiGeorge Chromosomal Region Homologous to the MouseTbx1Gene (Q24324759) (← links)
• Clinical, cytogenetic, and molecular characterization of seven patients with deletions of chromosome 22q13.3 (Q28237313) (← links)
• Analysis of chromosome 22 deletions in neurofibromatosis type 2-related tumors (Q30541671) (← links)
• Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects (Q33595838) (← links)
• Der(22)t(11;22) resulting from a paternal de novo translocation, adjacent 1 segregation, and maternal heterodisomy of chromosome 22. (Q33678031) (← links)
• The phenotypic effects of chromosome rearrangement involving bands 7q21.3 and 22q13.3 (Q33679632) (← links)
• Metachromatic leucodystrophy (MLD) in a patient with a constitutional ring chromosome 22. (Q33682593) (← links)
• A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q11. (Q35195482) (← links)
• Molecular definition of the 22q11 deletions in velo-cardio-facial syndrome (Q35642954) (← links)
• Minute supernumerary ring chromosome 22 associated with cat eye syndrome: further delineation of the critical region. (Q35643563) (← links)
• Molecular characterization of the marker chromosome associated with cat eye syndrome (Q35889314) (← links)
• Isolation of NotI sites from chromosome 22q11. (Q36721387) (← links)
• Isolation and mapping of cosmid markers on human chromosome 22, including one within the submicroscopically deleted region of DiGeorge syndrome (Q36721514) (← links)
• Sequence patterns and hybridization analysis of clones generated by Alu-PCR. (Q36729537) (← links)
• Anorectal malformation: the etiological factors (Q38434061) (← links)
• Constitutional DNA-level aberrations in chromosome 22 in a patient with multiple meningiomas. (Q40388570) (← links)
• Clinical and molecular studies in full trisomy 22: Further delineation of the phenotype and review of the literature (Q40440957) (← links)
• A radiation hybrid map of the region on human chromosome 22 containing the neurofibromatosis type 2 locus (Q41595616) (← links)
• Molecular analysis of a partial deletion of 22q in a central nervous system rhabdoid tumor (Q48440019) (← links)
• Red cell dimorphism in a young man with a constitutional chromosomal translocation t(11;22)(p15.5;q11.21) (Q58613903) (← links)
• Use of fluorescence in situ hybridization (FISH) in the diagnosis of DiGeorge sequence and related diseases (Q71088352) (← links)
• Mapping of the human lambda immunoglobulin variable gene subgroup 1 (Q72080548) (← links)