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Author: SSIEM
Publisher: Springer Science & Business Media
Published: 2012-01-13
Total Pages: 137
ISBN-13: 3642249353
DOWNLOAD EBOOKJIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder.
Author: SSIEM
Publisher: Springer Science & Business Media
Published: 2011-11-25
Total Pages: 123
ISBN-13: 364224758X
DOWNLOAD EBOOKJIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder.
Author: Johannes Zschocke
Publisher: Springer
Published: 2014-07-24
Total Pages: 164
ISBN-13: 3642541496
DOWNLOAD EBOOKJIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder or serve as an important reminder of clinical or biochemical features of a Mendelian disorder.
Author: Johannes Zschocke
Publisher: Springer Science & Business Media
Published: 2012-09-11
Total Pages: 133
ISBN-13: 3642324428
DOWNLOAD EBOOKJIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder.
Author: SSIEM
Publisher: Springer Science & Business Media
Published: 2012-02-01
Total Pages: 138
ISBN-13: 3642257518
DOWNLOAD EBOOKJIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder.
Author: SSIEM
Publisher: Springer Science & Business Media
Published: 2011-08-03
Total Pages: 133
ISBN-13: 3642177085
DOWNLOAD EBOOKJIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder.
Author: Johannes Zschocke
Publisher: Springer Science & Business Media
Published: 2012-12-18
Total Pages: 143
ISBN-13: 3642355188
DOWNLOAD EBOOKJIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder.
Author: SSIEM
Publisher: Springer Science & Business Media
Published: 2012-02-13
Total Pages: 130
ISBN-13: 364228096X
DOWNLOAD EBOOKJIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder.
Author: SSIEM
Publisher: Springer Science & Business Media
Published: 2012-05-10
Total Pages: 129
ISBN-13: 364228129X
DOWNLOAD EBOOKJIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder.
Author: Johannes Zschocke
Publisher: Springer Science & Business Media
Published: 2012-10-02
Total Pages: 155
ISBN-13: 3642334326
DOWNLOAD EBOOKJIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder.
