Petter Strömme: search on Z-Library

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51

Inspiratory impedance threshold valve during CPR

Audun Langhelle, Tævje Strømme, Kjetil Sunde, Lars Wik, Gunnar Nicolaysen, Petter Andreas Steen

Journal:

Year:

2002

Language:

english

File:

PDF, 153 KB

english, 2002

52

Molecular characterization of two deletion events involvingAlu-sequences, one novel base substitution and two tentative hotspot mutations in the hypoxanthine phosphoribosyltransferase (HPRT) gene in five patients with Lesch-Nyhan syndrome

T. Tvrdik, Suzanne Marcus, Sai-Mei Hou, Susann Fält, Peri Noori, Natalia Podlutskaja, Folker Hanefeld, Petter Strømme, Bo Lambert

Journal:

Year:

1998

Language:

english

File:

PDF, 124 KB

english, 1998

53

Blepharophimosis-ptosis-epicanthus inversus syndrome (BPES)

Petter Strømme, Frode Sandboe

Journal:

Acta Ophthalmologica (Blackwell)

Year:

1996

Language:

english

File:

PDF, 358 KB

english, 1996

54

A de novo 15q13.2q13.3 deletion in a boy with an Angelman syndrome like phenotype

Tuva Barøy, Doriana Misceo, Øivind Braaten, Johan R. Helle, Madeleine Fannemel, Petter Strømme, Eirik Frengen

Journal:

European Journal of Medical Genetics

Year:

2010

Language:

english

File:

PDF, 428 KB

english, 2010

55

Familial Hypomagnesemia—A Follow-Up Examination of Three Patients After 9 to 12 Years of Treatment

Strømme, Johan H, Steen-johnsen, Jon, Harnaes, Kristian, Hofstad, Fridjar, Brandtzaeg, Petter

Journal:

Pediatric Research

Year:

1981

Language:

english

File:

PDF, 2.89 MB

english, 1981

56

A novel type of rhizomelic chondrodysplasia punctata, RCDP5, is caused by loss of the PEX5 long isoform

Barøy, Tuva, Koster, Janet, Strømme, Petter, Ebberink, Merel S., Misceo, Doriana, Ferdinandusse, Sacha, Holmgren, Asbjørn, Hughes, Timothy, Merckoll, Else, Westvik, Jostein, Woldseth, Berit, Walter, J

Journal:

Human Molecular Genetics

Year:

2015

Language:

english

File:

PDF, 840 KB

english, 2015

57

Severe hypohidrotic ectodermal dysplasia in a girl caused by a de novo 9;X insertion that includes XIST and disrupts the EDA gene

Karen Helene Ørstavik, Gun Peggy S. Knudsen, Hilde Nordgarden, Eli Ormerod, Petter Strømme, Lazarous P. Lazarou, Lyndon G. Rosser, Trine Prescott, Gunnar Houge

Journal:

American Journal of Medical Genetics Part A

Year:

2007

Language:

english

File:

PDF, 158 KB

english, 2007

58

Apple peel intestinal atresia in siblings with ocular anomalies and microcephaly

Petter Strømme, Eilif Dahl, Tor Flage, Helge Stene-Johansen

Journal:

Clinical Genetics

Year:

1993

Language:

english

File:

PDF, 348 KB

english, 1993

59

Kaufman oculocerebrofacial syndrome in sisters with novel compound heterozygous mutation in UBE3B

Pedurupillay, Christeen Ramane J., Barøy, Tuva, Holmgren, Asbjørn, Blomhoff, Anne, Vigeland, Magnus D., Sheng, Ying, Frengen, Eirik, Strømme, Petter, Misceo, Doriana

Journal:

American Journal of Medical Genetics Part A

Year:

2015

Language:

english

File:

PDF, 6.73 MB

english, 2015

60

Learning disabilities and language pathology in patients with galactosemia

Rasmussen, Randi Korsvig, Andreassen, Anne Berit, Strømme, Petter, Hansen, Thor Willy Ruud

Journal:

Logopedics Phoniatrics Vocology

Year:

1996

Language:

english

File:

PDF, 622 KB

english, 1996

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