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M Peippo

Showing results (11-20 of 23) with videos related to

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European Journal of Human Genetics : EJHG|January 1, 1993
Striking founder effect for the fragile X syndrome in FinlandC Oudet, H von Koskull, A M Nordström, et al.
Duodecim; Laaketieteellinen Aikakauskirja|July 16, 2002
[Williams syndrome--developmental syndrome's common cardiovascular disorders]M Peippo, A Hiippala, M Raatikka, et al.
Journal of Medical Genetics|August 6, 2002
Cardiovascular manifestations in 75 patients with Williams syndromeM Eronen, M Peippo, A Hiippala, et al.
Pediatric Neurology|January 24, 2004
Temporo-occipital spikes: a typical EEG finding in Kabuki syndromeVirpi E Oksanen, Maria A Arvio, Maarit M Peippo, et al.
Genetic Counseling (Geneva, Switzerland)|November 3, 2004
De novo paracentric inversion 14q13q24.1 in a patient with severe involuntary movements, epilepsy, oligodontia and dysmorphic featuresM Peippo, C Tengström, M Arvio, et al.
Annals of the Rheumatic Diseases|January 18, 2002
Carriers of the aspartylglucosaminuria genetic mutation and chronic arthritisM Arvio, K Laiho, M Kauppi, et al.
American Journal of Medical Genetics. Part A|March 22, 2017
The HHID syndrome of hypertrichosis, hyperkeratosis, abnormal corpus callosum, intellectual disability, and minor anomalies is caused by mutations in ARID1BMarkus Zweier, Maarit M Peippo, Minna Pöyhönen, et al.
Journal of Medical Genetics|June 17, 2003
A new genetic locus for X linked progressive cone-rod dystrophyR Jalkanen, F Y Demirci, H Tyynismaa, et al.
Clinical Dysmorphology|March 15, 2006
Pitt-Hopkins syndrome in two patients and further definition of the phenotypeMaarit M Peippo, Kalle O J Simola, Leena K Valanne, et al.
Clinical Dysmorphology|April 2, 2004
Hypertrichosis, hyperkeratosis, abnormal corpus callosum, mental retardation and dysmorphic features in three unrelated femalesMinna H Pöyhönen, Maarit M Peippo, Leena K Valanne, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
European Journal of Human Genetics : EJHG|January 1, 1993
Striking founder effect for the fragile X syndrome in FinlandC Oudet, H von Koskull, A M Nordström, et al.
Duodecim; Laaketieteellinen Aikakauskirja|July 16, 2002
[Williams syndrome--developmental syndrome's common cardiovascular disorders]M Peippo, A Hiippala, M Raatikka, et al.
Journal of Medical Genetics|August 6, 2002
Cardiovascular manifestations in 75 patients with Williams syndromeM Eronen, M Peippo, A Hiippala, et al.
Pediatric Neurology|January 24, 2004
Temporo-occipital spikes: a typical EEG finding in Kabuki syndromeVirpi E Oksanen, Maria A Arvio, Maarit M Peippo, et al.
Genetic Counseling (Geneva, Switzerland)|November 3, 2004
De novo paracentric inversion 14q13q24.1 in a patient with severe involuntary movements, epilepsy, oligodontia and dysmorphic featuresM Peippo, C Tengström, M Arvio, et al.
Annals of the Rheumatic Diseases|January 18, 2002
Carriers of the aspartylglucosaminuria genetic mutation and chronic arthritisM Arvio, K Laiho, M Kauppi, et al.
American Journal of Medical Genetics. Part A|March 22, 2017
The HHID syndrome of hypertrichosis, hyperkeratosis, abnormal corpus callosum, intellectual disability, and minor anomalies is caused by mutations in ARID1BMarkus Zweier, Maarit M Peippo, Minna Pöyhönen, et al.
Journal of Medical Genetics|June 17, 2003
A new genetic locus for X linked progressive cone-rod dystrophyR Jalkanen, F Y Demirci, H Tyynismaa, et al.
Clinical Dysmorphology|March 15, 2006
Pitt-Hopkins syndrome in two patients and further definition of the phenotypeMaarit M Peippo, Kalle O J Simola, Leena K Valanne, et al.
Clinical Dysmorphology|April 2, 2004
Hypertrichosis, hyperkeratosis, abnormal corpus callosum, mental retardation and dysmorphic features in three unrelated femalesMinna H Pöyhönen, Maarit M Peippo, Leena K Valanne, et al.
Pageof 3