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Caries research, ISSN 0008-6568, 1967
Journal
2005, 3rd ed., ISBN 0198529783
eBook
1858, 61, [2] p., [2] leaves of plates (p. [2] at end advertisement)
Book
1997, 2nd ed., Oxford medical publications, ISBN 0192626922, ix, 214
Book
1994, 2nd ed., ISBN 8716109163, 421
Book
Science (Washington), ISSN 0036-8075, 11/2010, Volume 330, Issue 6005, pp. 732 - 732
Journal Article
Nature, ISSN 0028-0836, 05/2019, Volume 569, Issue 7757, pp. 459 - 459
Journal Article
Clinical Genetics, ISSN 0009-9163, 04/2017, Volume 91, Issue 4, pp. 507 - 519
Constitutional mismatch repair (MMR) deficiency (CMMRD) is a rare childhood cancer susceptibility syndrome resulting from biallelic germline loss‐of‐function... 
acute myeloid leukaemia | neurofibromatosis type 1 | childhood cancer | constitutional mismatch repair deficiency | high‐grade glioma | café‐au‐lait spot | rhabdomyosarcoma | germline mutation | mismatch repair gene | high-grade glioma | café-au-lait spot | COMPOUND-HETEROZYGOUS MUTATIONS | LYNCH-SYNDROME | HEMATOLOGICAL MALIGNANCY | GLIOBLASTOMA-MULTIFORME | MICROSATELLITE INSTABILITY | cafe-au-lait spot | EUROPEAN CONSORTIUM CARE | GENETICS & HEREDITY | EARLY-ONSET | GERMLINE MUTATIONS | BIALLELIC PMS2 MUTATIONS | AU-LAIT SPOTS | Neoplastic Syndromes, Hereditary - pathology | Glioma - diagnosis | Neurofibromatosis 1 - epidemiology | Colorectal Neoplasms - genetics | Humans | Brain Neoplasms - pathology | Child, Preschool | Rhabdomyosarcoma - pathology | DNA Mismatch Repair - genetics | Cafe-au-Lait Spots - diagnosis | Colorectal Neoplasms - diagnosis | Glioma - genetics | Neoplastic Syndromes, Hereditary - epidemiology | Glioma - pathology | Germ-Line Mutation | Neoplastic Syndromes, Hereditary - genetics | Neurofibromatosis 1 - genetics | Colorectal Neoplasms - epidemiology | Cafe-au-Lait Spots - genetics | Diagnosis, Differential | Rhabdomyosarcoma - diagnosis | Leukemia, Myeloid, Acute - pathology | Brain Neoplasms - diagnosis | Brain Neoplasms - genetics | Neoplastic Syndromes, Hereditary - diagnosis | Neurofibromatosis 1 - diagnosis | Cafe-au-Lait Spots - physiopathology | Neurofibromatosis 1 - pathology | Phenotype | Leukemia, Myeloid, Acute - diagnosis | Rhabdomyosarcoma - genetics | Colorectal Neoplasms - pathology | Brain Neoplasms - epidemiology | Leukemia, Myeloid, Acute - genetics | Medical research | Gene mutations | Gliomas | Neurofibromatosis | Leukemia | Medicine, Experimental | Disease susceptibility | Pediatrics | Genotype & phenotype | Medical diagnosis | Cancer
Journal Article
PLoS ONE, ISSN 1932-6203, 09/2015, Volume 10, Issue 9, p. e0138207
Journal Article
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