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O Rittinger

Showing results (1-10 of 24) with videos related to

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Klinische Padiatrie|June 22, 2001
[Clinical aspects and genetics of Prader-Willi syndrome]O Rittinger
Padiatrie Und Padologie|January 1, 1984
[Maternal phenylketonuria]O Rittinger, E Plöchl, E Jarosch
Clinical Dysmorphology|October 26, 1999
Bilateral hydronephrosis due to megacalicosis as a prenatal sonographic finding in a female with Schinzel-Giedion syndromeO Rittinger, P Weiss-Wichert, G Hasenöhrl
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 15, 2003
Malignant astrocytoma arising 10 years after combined treatment of craniopharyngiomaO Rittinger, M Kranzinger, R Jones, et al.
Klinische Padiatrie|November 1, 1991
[Neonatal form of a nonketotic hyperglycinemia in consanguinous parents]E Plöchl, O Rittinger, E Doringer, et al.
Klinische Padiatrie|May 1, 1997
A Turner-like phenotype in a girl with an isodicentric fluorescent Y chromosome mosaicismE Bergendi, E Plöchl, I Vlasak, et al.
Cytogenetic and Genome Research|March 9, 2004
De novo 9-break-event in one chromosome 21 combined with a microdeletion in 21q22.11 in a mentally retarded boy with short statureA Weise, O Rittinger, H Starke, et al.
Klinische Padiatrie|September 17, 2005
[Menkes' disease: heterozygosity testing by quantitative real-time PCR and the dilemma of therapeutic support]O Rittinger, G Sander, A Schaller, et al.
Ophthalmology|February 5, 2005
Ocular manifestations of keratitis-ichthyosis-deafness (KID) syndromeE M Messmer, K R Kenyon, O Rittinger, et al.
American Journal of Medical Genetics|July 12, 1996
Regional localization of two MRX genes to Xq28 (MRX28) and to Xp11.4-Xp22.12 (MRX33)E Holinski-Feder, A Golla, I Rost, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Klinische Padiatrie|June 22, 2001
[Clinical aspects and genetics of Prader-Willi syndrome]O Rittinger
Padiatrie Und Padologie|January 1, 1984
[Maternal phenylketonuria]O Rittinger, E Plöchl, E Jarosch
Clinical Dysmorphology|October 26, 1999
Bilateral hydronephrosis due to megacalicosis as a prenatal sonographic finding in a female with Schinzel-Giedion syndromeO Rittinger, P Weiss-Wichert, G Hasenöhrl
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 15, 2003
Malignant astrocytoma arising 10 years after combined treatment of craniopharyngiomaO Rittinger, M Kranzinger, R Jones, et al.
Klinische Padiatrie|November 1, 1991
[Neonatal form of a nonketotic hyperglycinemia in consanguinous parents]E Plöchl, O Rittinger, E Doringer, et al.
Klinische Padiatrie|May 1, 1997
A Turner-like phenotype in a girl with an isodicentric fluorescent Y chromosome mosaicismE Bergendi, E Plöchl, I Vlasak, et al.
Cytogenetic and Genome Research|March 9, 2004
De novo 9-break-event in one chromosome 21 combined with a microdeletion in 21q22.11 in a mentally retarded boy with short statureA Weise, O Rittinger, H Starke, et al.
Klinische Padiatrie|September 17, 2005
[Menkes' disease: heterozygosity testing by quantitative real-time PCR and the dilemma of therapeutic support]O Rittinger, G Sander, A Schaller, et al.
Ophthalmology|February 5, 2005
Ocular manifestations of keratitis-ichthyosis-deafness (KID) syndromeE M Messmer, K R Kenyon, O Rittinger, et al.
American Journal of Medical Genetics|July 12, 1996
Regional localization of two MRX genes to Xq28 (MRX28) and to Xp11.4-Xp22.12 (MRX33)E Holinski-Feder, A Golla, I Rost, et al.
Pageof 3