Hannaleena, Kokkonen: search on Z-Library

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1

Clinical first-trimester routine screening for Down syndrome in singleton pregnancies in northern Finland

Yrtti Valinen, Katrin Rapakko, Hannaleena Kokkonen, Paivi Laitinen, Aydin Tekay, Tarja Ahola, Markku Ryynanen

Journal:

American Journal of Obstetrics and Gynecology

Year:

2007

Language:

english

File:

PDF, 99 KB

english, 2007

2

Biogenesis of the mitochondrial respiratory chain in children with severe multiorgan disorders

Reetta Hinttala, Johanna Uusimaa, Hana Antonicka, Hannaleena Kokkonen, Jukka S. Moilanen, Heikki Rantala, Kari Majamaa, Eric A. Shoubridge

Journal:

Year:

2012

Language:

english

File:

PDF, 58 KB

english, 2012

3

Infantile spasms and 15q11.2q13.1 chromosome duplication in two successive generations

Riikonen, Raili Sylvia, Wallden, Tiina, Kokkonen, Hannaleena

Journal:

European Journal of Paediatric Neurology

Year:

2016

Language:

english

File:

PDF, 444 KB

english, 2016

4

Report of interstitial 22q13.1q13.2 microduplication in two siblings with distinctive dysmorphic features, heart defect and mental retardation

Rahikkala, Elisa, Forsström, Linda M., Kokkonen, Hannaleena, Knuutila, Sakari, Mustonen, Aki, Ignatius, Jaakko

Journal:

European Journal of Medical Genetics

Year:

2013

Language:

english

File:

PDF, 1.81 MB

english, 2013

5

An unexpected recurrence of Angelman syndrome suggestive of maternal germ-line mosaicism of del(15)(q11q13) in a Finnish family

Hannaleena Kokkonen, Jaakko Leisti

Journal:

Year:

2000

Language:

english

File:

PDF, 37 KB

english, 2000

6

False-Negative Results in Routine Combined First-Trimester Screening for Down Syndrome in Finland

Marttala, Jaana, Kaijomaa, Marja, Ranta, Jenni, Dahlbacka, Anna, Nieminen, Pentti, Tekay, Aydin, Kokkonen, Hannaleena, Laitinen, Paivi, Ignatius, Jaakko, Romppanen, Jarkko, Heinonen, Seppo, Jarvela, I

Journal:

American Journal of Perinatology

Year:

2012

Language:

english

File:

PDF, 112 KB

english, 2012

7

A homozygous I684T in GLE1 as a novel cause of arthrogryposis and motor neuron loss

Paakkola, Teija, Vuopala, Katri, Kokkonen, Hannaleena, Ignatius, Jaakko, Valkama, Marita, Moilanen, Jukka S., Fahiminiya, Somayyeh, Majewski, Jacek, Hinttala, Reetta, Uusimaa, Johanna

Journal:

Clinical Genetics

Year:

2017

Language:

english

File:

PDF, 1.31 MB

english, 2017

8

Decreased binding of [11C]flumazenil in Angelman syndrome patients with GABAA receptor β3 subunit deletions

Irma E. Holopainen, E.-Liisa Metsähonkala, Hannaleena Kokkonen, Riitta K. Parkkola, Tuula E. Manner, Kjell Någren, Esa R. Korpi

Journal:

Annals of Neurology

Year:

2001

Language:

english

File:

PDF, 6.37 MB

english, 2001

9

UBE3A gene mutations in finnish Angelman syndrome patients detected by conformation sensitive gel electrophoresis

Katrin Rapakko, Hannaleena Kokkonen, Jaakko Leisti

Journal:

American Journal of Medical Genetics Part A

Year:

2004

Language:

english

File:

PDF, 98 KB

english, 2004

10

Screening for large genomic rearrangements in the FANCA gene reveals extensive deletion in a Finnish breast cancer family

Szilvia Solyom, Robert Winqvist, Jenni Nikkilä, Katrin Rapakko, Pasi Hirvikoski, Hannaleena Kokkonen, Katri Pylkäs

Journal:

Year:

2011

Language:

english

File:

PDF, 720 KB

english, 2011

11

More invasive procedures are done to detect each case of Down's syndrome in younger women

JAANA MARTTALA, JENNI K. RANTA, MARJA KAIJOMAA, PENTTI NIEMINEN, PAIVI LAITINEN, HANNALEENA KOKKONEN, JARKKO ROMPPANEN, ESA HAMALAINEN, JOHANNA KULTTI, AYDIN TEKAY, VELI-MATTI ULANDER, TIMPPA HONKASAL

Journal:

Acta Obstetricia et Gynecologica Scandinavica

Year:

2011

Language:

english

File:

PDF, 226 KB

english, 2011

12

Combined First-Trimester Screening in Northern Finland: Experiences of the First Ten Years

Anna, Merilainen, Sini, Peuhkurinen, Timppa, Honkasalo, Paivi, Laitinen, Hannaleena, Kokkonen, Markku, Ryynanen, Jaana, Marttala

Journal:

Clinical Medicine Insights Reproductive Health

Year:

2014

Language:

english

File:

PDF, 251 KB

english, 2014

13

A molecular and cytogenetic study in Finnish Prader-Willi patients

Hannaleena Kokkonen, Marketta Kähkönen, Jaakko Leisti

Journal:

Year:

1995

Language:

english

File:

PDF, 424 KB

english, 1995

14

An unexpected recurrence of Angelman syndrome suggestive of maternal germ-line mosaicism of del(15)(q11q13) in a Finnish family

Hannaleena Kokkonen,Jaakko Leisti

Journal:

Year:

2000

Language:

english

File:

PDF, 37 KB

english, 2000

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