FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Frédérique Tihy

Research Profile

Procedures

Disorders

Anatomy

Chemicals & Drugs

Physiology

Living Beings

Infants

Co-author Network

Publications

TOP 3
Jennifer Gignac; Karine Danis; Frédérique Tihy; Emmanuelle Lemyre
Prenatal detection of subtelomeric rearrangements by multi-subtelomere FISH in a cohort of fetuses with major malformations.
Meaghan Hysert; Hélène Bruyère; Gilbert B. Côté; Angelika J Dawson; Jo-Anna Dolling; raouf fetni; Monica Hrynchak; Josée Lavoie; Jean McGowan-Jordan; Frédérique Tihy; Alessandra M V Duncan
Prenatal cytogenetic assessment and inv(2)(p11.2q13).
Volkan Seyrantepe; Frédérique Tihy; Alexey V Pshezhetsky
The microcell-mediated transfer of human chromosome 8 restores the deficient N-acetylytransferase activity in skin fibroblasts of Mucopolysaccharidosis type IIIC patients.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Frédérique Tihy (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2006: Jennifer Gignac; Karine Danis; Frédérique Tihy; Emmanuelle Lemyre
Prenatal detection of subtelomeric rearrangements by multi-subtelomere FISH in a cohort of fetuses with major malformations.
American journal of medical genetics. Part A 2006;140(24):2768-75.
2006: Meaghan Hysert; Hélène Bruyère; Gilbert B. Côté; Angelika J Dawson; Jo-Anna Dolling; raouf fetni; Monica Hrynchak; Josée Lavoie; Jean McGowan-Jordan; Frédérique Tihy; Alessandra M V Duncan
Prenatal cytogenetic assessment and inv(2)(p11.2q13).
Prenatal diagnosis 2006;26(9):810-3.
2006: Volkan Seyrantepe; Frédérique Tihy; Alexey V Pshezhetsky
The microcell-mediated transfer of human chromosome 8 restores the deficient N-acetylytransferase activity in skin fibroblasts of Mucopolysaccharidosis type IIIC patients.
Human genetics 2006;120(2):293-6.
2005: Frédérique Tihy; Nicole Lemieux; Emmanuelle Lemyre
Complex chromosome rearrangement and recombinant balanced translocation in a mother and a daughter with the same phenotypic abnormalities.
American journal of medical genetics. Part A 2005;135(3):317-9.
2000: Frédérique Tihy; Emmanuelle Lemyre; Louis Dallaire; Nicole Lemieux
Supernumerary chromosome inherited from a maternal balanced translocation leading to pure trisomy 9p.
American journal of medical genetics 2000;91(5):383-6.
1999: Frédérique Tihy; Emmanuelle Lemyre; Nicole Lemieux; Louis Dallaire
De novo dup(X)(q22.1q25) in a girl with an abnormal phenotype.
American journal of medical genetics 1999;87(4):302-5.
1999: L Caron; Frédérique Tihy; Louis Dallaire
Frequencies of chromosomal abnormalities at amniocentesis: over 20 years of cytogenetic analyses in one laboratory.
American journal of medical genetics 1999;82(2):149-54.
1998: Frédérique Tihy; patrick scott; P Russo; Martin A Champagne; J C Tabet; Nicole Lemieux
Cytogenetic analysis of a parachordoma.
Cancer genetics and cytogenetics 1998;105(1):14-9.
1996: C H Kos; Frédérique Tihy; Heini Murer; Nicole Lemieux; Harriet S Tenenhouse
Comparative mapping of Na+-phosphate cotransporter genes, NPT1 and NPT2, in human and rabbit.
Cytogenetics and cell genetics 1996;75(1):22-4.
1996: Frédérique Tihy; Nicole Lemieux; M Lombard; Bernard Dutrillaux
Comparative RB1 gene mapping in Homo sapiens, Pithecia pithecia, Macaca sylvana, and Cercopithecus aethiops tantalus.
Cytogenetics and cell genetics 1996;72(1):9-11.
1994: Frédérique Tihy; Nicolas Vogt; Dominique Recan; Bernard Malfoy; France Leturcq; M Coquet; F Serville; D Fontan; Jean-Michel Guillard; Jean-Claude Kaplan
Skewed inactivation of an X chromosome deleted at the dystrophin gene in an asymptomatic mother and her affected daughter.
Human genetics 1994;93(5):563-7.
1994: C H Kos; Frédérique Tihy; Michael J Econs; Heini Murer; Nicole Lemieux; Harriet S Tenenhouse
Localization of a renal sodium-phosphate cotransporter gene to human chromosome 5q35.
Genomics 1994;19(1):176-7.
1993: M Labuda; Nicole Lemieux; Frédérique Tihy; C Prinster; Francis Glorieux
Human 25-hydroxyvitamin D 24-hydroxylase cytochrome P450 subunit maps to a different chromosomal location than that of pseudovitamin D-deficient rickets.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 1993;8(11):1397-406.
1992: Frédérique Tihy; M Kress; M Harper; Bernard Dutrillaux; Nicole Lemieux
Localization of the human kinesin-related gene to band 10q24 by fluorescence in situ hybridization.
Genomics 1992;13(4):1371-2.