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DISCISSION OF THE ECTOPIC CRYSTALLINE LENS

Bulletin des societes d'ophtalmologie de France, 1964-04, Vol.64, p.420

1964

Volltextzugriff (PDF)

Apropos of a case of fat embolism

Bulletin des societes d'ophtalmologie de France, 1968-07, Vol.68 (7), p.690

1968

Volltextzugriff (PDF)

Fat embolism during a nephrotic syndrome in a 4-year-old girl

La Nouvelle presse medicale, 1973-05, Vol.2 (19), p.1308

1973

Volltextzugriff (PDF)

Fundus oculi in hyperlipidemia

Bulletin des societes d'ophtalmologie de France, 1969-04, Vol.69 (4), p.491

1969

Volltextzugriff (PDF)

NUP98 is rearranged in 3.8% of pediatric AML forming a clinical and molecular homogenous group with a poor prognosis

Leukemia, 2017-03, Vol.31 (3), p.565-572

2017

Volltextzugriff (PDF)

Letter: Influence of tobacco smoke on the pressure of the central artery of the retina

La Nouvelle presse medicale, 1976-07, Vol.5 (27), p.1699

1976

Volltextzugriff (PDF)

Influence of tobacco smoke on the pressure of the central retinal artery

Bulletin des societes d'ophtalmologie de France, 1976-07, Vol.76 (7-8), p.675

1976

Volltextzugriff (PDF)

Pregnancy outcomes of prenatally diagnosed Turner syndrome: a French multicenter retrospective study including a series of 975 cases

Prenatal diagnosis, 2014-12, Vol.34 (12), p.1133-1138

2014

Volltextzugriff (PDF)

Microdeletion at chromosome 4q21 defines a new emerging syndrome with marked growth restriction, mental retardation and absent or severely delayed speech

Journal of medical genetics, 2010-06, Vol.47 (6), p.377-384

2010

Volltextzugriff (PDF)

Prognosis of inv(16)/t(16;16) acute myeloid leukemia (AML): a survey of 110 cases from the French AML Intergroup

Blood, 2003-07, Vol.102 (2), p.462-469

2003

Volltextzugriff (PDF)

Acute myeloid leukaemia with 8p11 ( ) rearrangement: an integrated cytologic, cytogenetic and molecular study by the groupe francophone de cytogénétique hématologique

Leukemia, 2008-08, Vol.22 (8), p.1567-1575

2008

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Endogenous retroviral sequence is fused to FGFR1 kinase in the 8p12 stem-cell myeloproliferative disorder with t(8;19)(p12;q13.3)

Blood, 2003-01, Vol.101 (1), p.286-288

2003

Volltextzugriff (PDF)

Refining the critical region for congenital diaphragmatic hernia on chromosome 15q26 from the study of four fetuses

Prenatal diagnosis, 2011-09, Vol.31 (9), p.912-914

2011

Volltextzugriff (PDF)

What can we learn from old microdeletion syndromes using array-CGH screening?

Clinical genetics, 2012-07, Vol.82 (1), p.41-47

2012

Volltextzugriff (PDF)

M0 AML, clinical and biologic features of the disease, including AML1 gene mutations: a report of 59 cases by the Groupe Français d'Hématologie Cellulaire (GFHC) and the Groupe Français de Cytogénétique Hématologique (GFCH)

Blood, 2003-02, Vol.101 (4), p.1277-1283

2003

Volltextzugriff (PDF)

Polymicrogyria in a child with inv dup del(9p) and 22q11.2 microduplication

American journal of medical genetics. Part A, 2009-03, Vol.149A (3), p.475-481

2009

Volltextzugriff (PDF)

Untreated growth hormone deficiency with extremely short stature, bone dysplasia, cleft lip–palate and severe mental retardation in a 26-year-old man with a de novo unbalanced translocation t(1;12)(q24;q24)

European journal of medical genetics, 2007-11, Vol.50 (6), p.455-464

2007

Volltextzugriff (PDF)

Chromosomal factors of infertility in candidate couples for ICSI: an equal risk of constitutional aberrations in women and men

Human reproduction (Oxford), 2001-01, Vol.16 (1), p.82-90

2001

Volltextzugriff (PDF)

X-linked recessive ichthyosis in a girl: strategy for identifying the causal mechanism

British journal of dermatology (1951), 2005-01, Vol.152 (1), p.191-193

2005

Volltextzugriff (PDF)

MLL amplification in myeloid leukemias: A study of 14 cases with multiple copies of 11q23

Genes chromosomes & cancer, 2000-09, Vol.29 (1), p.40-47

2000

Volltextzugriff (PDF)

Cytogenetic abnormalities in adult acute lymphoblastic leukemia : Correlations with hematologic findings and outcome. A collaborative study of the Groupe Français de Cytogénétique Hématologique

Blood, 1996-04, Vol.87 (8), p.3135-3142

1996

Volltextzugriff (PDF)

MLL amplification in acute leukaemia : A United Kingdom cancer cytogenetics group (UKCCG) study

Leukemia, 2000-11, Vol.14 (11), p.1885-1891

2000

Volltextzugriff (PDF)

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DISCISSION OF THE ECTOPIC CRYSTALLINE LENS

Apropos of a case of fat embolism

Fat embolism during a nephrotic syndrome in a 4-year-old girl

Fundus oculi in hyperlipidemia

NUP98 is rearranged in 3.8% of pediatric AML forming a clinical and molecular homogenous group with a poor prognosis

Letter: Influence of tobacco smoke on the pressure of the central artery of the retina

Influence of tobacco smoke on the pressure of the central retinal artery

Pregnancy outcomes of prenatally diagnosed Turner syndrome: a French multicenter retrospective study including a series of 975 cases

Microdeletion at chromosome 4q21 defines a new emerging syndrome with marked growth restriction, mental retardation and absent or severely delayed speech

Prognosis of inv(16)/t(16;16) acute myeloid leukemia (AML): a survey of 110 cases from the French AML Intergroup

Report of 34 patients with clonal chromosomal abnormalities in Philadelphia-negative cells during imatinib treatment of Philadelphia-positive chronic myeloid leukemia

Acute myeloid leukaemia with 8p11 ( ) rearrangement: an integrated cytologic, cytogenetic and molecular study by the groupe francophone de cytogénétique hématologique

Endogenous retroviral sequence is fused to FGFR1 kinase in the 8p12 stem-cell myeloproliferative disorder with t(8;19)(p12;q13.3)

Refining the critical region for congenital diaphragmatic hernia on chromosome 15q26 from the study of four fetuses

Molecular characterization of 39 de novo sSMC: contribution to prognosis and genetic counselling, a prospective study

What can we learn from old microdeletion syndromes using array-CGH screening?

M0 AML, clinical and biologic features of the disease, including AML1 gene mutations: a report of 59 cases by the Groupe Français d'Hématologie Cellulaire (GFHC) and the Groupe Français de Cytogénétique Hématologique (GFCH)

Polymicrogyria in a child with inv dup del(9p) and 22q11.2 microduplication

Untreated growth hormone deficiency with extremely short stature, bone dysplasia, cleft lip–palate and severe mental retardation in a 26-year-old man with a de novo unbalanced translocation t(1;12)(q24;q24)

Chromosomal factors of infertility in candidate couples for ICSI: an equal risk of constitutional aberrations in women and men

A French collaborative survey of 272 fetuses with 22q11.2 deletion: ultrasound findings, fetal autopsies and pregnancy outcomes: Prenatal diagnosis of the 22q11.2 deletion of 272 fetuses

X-linked recessive ichthyosis in a girl: strategy for identifying the causal mechanism

MLL amplification in myeloid leukemias: A study of 14 cases with multiple copies of 11q23

Cytogenetic abnormalities in adult acute lymphoblastic leukemia : Correlations with hematologic findings and outcome. A collaborative study of the Groupe Français de Cytogénétique Hématologique

MLL amplification in acute leukaemia : A United Kingdom cancer cytogenetics group (UKCCG) study

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