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British Journal of Haematology
|
May 29, 2010
Malignancies and survival patterns in the National Cancer Institute inherited bone marrow failure syndromes cohort study
Blanche P Alter, Neelam Giri, Sharon A Savage, et al.
Pediatric Blood & Cancer
|
July 19, 2016
Otologic manifestations of Fanconi anemia and other inherited bone marrow failure syndromes
Adedoyin Kalejaiye, Neelam Giri, Carmen C Brewer, et al.
Oral Diseases
|
October 22, 2008
Oral and dental phenotype of dyskeratosis congenita
J C Atkinson, K E Harvey, D L Domingo, et al.
The Journal of Pediatrics
|
December 13, 2000
Successful bone marrow transplantation in a patient with Schimke immuno-osseous dysplasia
E M Petty, G A Yanik, R J Hutchinson, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 10, 2015
Endocrine disorders in Fanconi anemia: recommendations for screening and treatment
Anna Petryk, Roopa Kanakatti Shankar, Neelam Giri, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 22, 2016
Research participant interest in primary, secondary, and incidental genomic findings
Jennifer T Loud, Renee C Bremer, Phuong L Mai, et al.
The Journal of Pediatrics
|
August 17, 2002
Shwachman-Diamond syndrome: report from an international conference
Robert Rothbaum, Jean Perrault, Adrianna Vlachos, et al.
Blood
|
May 1, 2007
Very short telomere length by flow fluorescence in situ hybridization identifies patients with dyskeratosis congenita
Blanche P Alter, Gabriela M Baerlocher, Sharon A Savage, et al.
Blood
|
August 1, 1993
Treatment of Diamond-Blackfan anemia with recombinant human interleukin-3
A P Gillio, L B Faulkner, B P Alter, et al.
Stem Cells (Dayton, Ohio)
|
July 1, 1993
Successful treatment of Diamond-Blackfan anemia with interleukin 3
A P Gillio, L B Faulkner, B P Alter, et al.
Page
of 37
Search research articles
Search
Showing results (291-300 of 362) with videos related to
Sort By:
Page
of 37
British Journal of Haematology
|
May 29, 2010
Malignancies and survival patterns in the National Cancer Institute inherited bone marrow failure syndromes cohort study
Blanche P Alter, Neelam Giri, Sharon A Savage, et al.
Pediatric Blood & Cancer
|
July 19, 2016
Otologic manifestations of Fanconi anemia and other inherited bone marrow failure syndromes
Adedoyin Kalejaiye, Neelam Giri, Carmen C Brewer, et al.
Oral Diseases
|
October 22, 2008
Oral and dental phenotype of dyskeratosis congenita
J C Atkinson, K E Harvey, D L Domingo, et al.
The Journal of Pediatrics
|
December 13, 2000
Successful bone marrow transplantation in a patient with Schimke immuno-osseous dysplasia
E M Petty, G A Yanik, R J Hutchinson, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 10, 2015
Endocrine disorders in Fanconi anemia: recommendations for screening and treatment
Anna Petryk, Roopa Kanakatti Shankar, Neelam Giri, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 22, 2016
Research participant interest in primary, secondary, and incidental genomic findings
Jennifer T Loud, Renee C Bremer, Phuong L Mai, et al.
The Journal of Pediatrics
|
August 17, 2002
Shwachman-Diamond syndrome: report from an international conference
Robert Rothbaum, Jean Perrault, Adrianna Vlachos, et al.
Blood
|
May 1, 2007
Very short telomere length by flow fluorescence in situ hybridization identifies patients with dyskeratosis congenita
Blanche P Alter, Gabriela M Baerlocher, Sharon A Savage, et al.
Blood
|
August 1, 1993
Treatment of Diamond-Blackfan anemia with recombinant human interleukin-3
A P Gillio, L B Faulkner, B P Alter, et al.
Stem Cells (Dayton, Ohio)
|
July 1, 1993
Successful treatment of Diamond-Blackfan anemia with interleukin 3
A P Gillio, L B Faulkner, B P Alter, et al.
Page
of 37