13 results on '"Jennings, Lawrence J."'
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2. Normalization of NPM1 mutant transcript to the wild‐type transcript
3. Congenital central hypoventilation syndrome: Severe disease caused by co‐occurrence of two PHOX2B variants inherited separately from asymptomatic family members
4. The classification of pediatric and young adult renal cell carcinomas registered on the children's oncology group (COG) protocol AREN03B2 after focused genetic testing
5. Early mixed T-cell chimerism is predictive of pediatric AML or MDS relapse after hematopoietic stem cell transplant
6. Expanding the spectrum ofALK-rearranged renal cell carcinomas in children: Identification of a novelHOOK1-ALKfusion transcript
7. ALK-rearranged renal cell carcinomas in children
8. Gain of 1q is associated with inferior event-free and overall survival in patients with favorable histology Wilms tumor: A report from the Children's Oncology Group
9. Germline mosaicism ofPHOX2Bmutation accounts for familial recurrence of congenital central hypoventilation syndrome (CCHS)
10. Mammary Analogue Secretory Carcinoma of the Parotid Gland in a Pediatric Patient
11. Variable human phenotype associated with novel deletions of thePHOX2Bgene
12. Agminated presentation of fusion-driven melanocytic neoplasms.
13. Mammary analogue secretory carcinoma of the parotid gland in a pediatric patient.
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