C R Bryke
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Explore the profile of C R Bryke including associated specialties, affiliations and a list of published articles.
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Articles
12
Citations
117
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Recent Articles
1.
Chorzalska A, Salloum I, Shafqat H, Khan S, Marjon P, Treaba D, et al.
Leukemia
. 2014 Apr;
28(11):2165-77.
PMID: 24699303
The basis for persistence of leukemic stem cells in the bone marrow microenvironment remains poorly understood. We present evidence that signaling cross-talk between α4 integrin and Abelson interactor-1 (Abi-1) is...
2.
Lloyd A, Ragosta K, Bryke C, Hoo J
Am J Med Genet A
. 2006 Apr;
140(11):1253-5.
PMID: 16642505
No abstract available.
3.
Bellus G, Spector E, Speiser P, Weaver C, GARBER A, Bryke C, et al.
Am J Hum Genet
. 2000 Oct;
67(6):1411-21.
PMID: 11055896
The fibroblast growth factor-receptor 3 (FGFR3) Lys650 codon is located within a critical region of the tyrosine kinase-domain activation loop. Two missense mutations in this codon are known to result...
4.
Shohat M, Lachman R, Gruber H, HSIA Y, Golbus M, Witt D, et al.
Am J Med Genet
. 1994 Aug;
52(1):9-18.
PMID: 7977470
To further characterize the clinical, radiographic and chondro-osseous morphologic changes in the Desbuquois syndrome, 7 patients from three sibships are described. They all had prenatal onset severe rhizomelic and mesomelic...
5.
Lindgren V, Bryke C, Ozcelik T, Yang-Feng T, Francke U
Am J Hum Genet
. 1992 May;
50(5):988-97.
PMID: 1315124
We have studied three patients, one with extensive polyposis of the colon, who have constitutional interstitial deletions of the long arm of chromosome 5. High-resolution banding studies indicated that the...
6.
Lindgren V, Chen C, Bryke C, Lichter P, Page D, Yang-Feng T
Hum Genet
. 1992 Feb;
88(4):393-8.
PMID: 1740316
Cytogenetic and molecular techniques were employed to determine the origin of marker chromosomes in five patients with mosaic 45,X karyotypes. The markers were shown to be derived from the X...
7.
Bryke C, Lindgren V, Fryburg J, Yang-Feng T
Am J Med Genet
. 1990 Jun;
36(2):247-50.
PMID: 2368814
A previously unreported isodicentric chromosome 18 was discovered in an abnormal infant boy whose mosaic karyotype was 46,XY/46,XY,-18,+idic(18)(q12.2). His constellation of congenital anomalies was typical of the 18q-syndrome. The clinical...
8.
Bryke C, BREG W, Potluri V, Yang-Feng T
Am J Med Genet
. 1990 May;
36(1):43-4.
PMID: 2333906
A family with an unusual variant of chromosome 16 is presented. The mother and son both with additional material present in the short arm of chromosome 16 adjacent to the...
9.
Bryke C, Mahoney M, Yang-Feng T
Am J Med Genet
. 1989 Oct;
34(2):207-10.
PMID: 2816999
A diagnosis of 45,X/48,XYYY was made antenatally. Counseling this case was hampered by the paucity of literature describing the phenotype of patients with this chromosome constitution. The fetus had ambiguous...
10.
Bryke C, Tunnessen Jr W, SCULLY T, Oski F
Pediatrics
. 1988 Nov;
82(5):752-5.
PMID: 3186356
Patient, contact data, collected by two first year pediatric residents, separated in time by 25 years, were compared, and it is concluded that pediatric residency has undergone major changes throughout...