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THE AFRICAN MUS (PIGMY-MICE): THE ROLE OF CHROMOSOMAL POLYMORPHISM IN SPECIATIONJOTTERAND M.1975; CARYOLOGIA; ITAL.; DA. 1975; VOL. 28; NO 3; PP. 335-344; BIBL. 1 P.Article

A CHROMOSOME MUTATION AFFECTING THE NUMBER OF NUCLEOLI IN XENOPUS BOREALIS PARKER = MUTATION CHROMOSOMIQUE AFFECTANT LE NOMBRE DE NUCLEOLES CHEZ X. B. PARKERJOTTERAND M; FISCHBERG M.1974; EXPERIENTIA; SUISSE; DA. 1974; VOL. 30; NO 9; PP. 1003-1005; ABS. FR.; BIBL. 8 REF.Article

Cytogénétique des hémopathies malignes = Cytogenetics of malignant hemopathiesJOTTERAND, M.Médecine et hygiène. 2002, Vol 60, Num 2389, pp 838-842, issn 0025-6749Article

A NEW CASE OF TRISOMY FOR THE DISTAL PART OF 13Q DUE TO MATERNAL TRANSLOCATION, T(9;13) (P21;Q21).JOTTERAND M; JUILLARD E.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 33; NO 3; PP. 213-222; BIBL. 20 REF.Article

LA MANUL OTOCOLOBUS MANUL (PALLAS1776): SON CARYOTYPE ET SA POSITION DANS LA CLASSIFICATION DES FELIDESSCHAUENBERG P; JOTTERAND M.1975; REV. SUISSE ZOOL.; SUISSE; DA. 1975; VOL. 82; NO 2; PP. 425-429; BIBL. 5REFArticle

L'ANALYSE DU CARYOTYPE PERMET DE RECONNAITRE DEUX ESPECES CRYPTIQUES CONFONDUES SOUS LE NOM DE TATERILLUS GRACILIS TH. (RONGEURS-GERBILLIDAE)MATTHEY R; JOTTERAND M.1972; MAMMALIA; FR.; DA. 1972; VOL. 36; NO 2; PP. 193-209; H.T. 6; ABS. ANGL.; BIBL. 14 REF.Serial Issue

FAUSSES-COUCHES PRECOCES ITERATIVES ET CARYOTYPE. ETUDE CYTOGENETIQUE DE 80 COUPLES CONSECUTIFSPESCIA G; JOTTERAND M; GAIDE AC et al.1979; J. GYNECOL. OBSTETR. BIOL. REPROD.; FRA; DA. 1979; VOL. 8; NO 1; PP. 35-38; ABS. ENG; BIBL. 16 REF.Article

A CASE OF (9P+,13Q-) TRANSLOCATION. CYTOGENETICS AND FAMILY HISTORYJOTTERAND M; CATTI A; JUILLARD E et al.1975; ARCH. GENET.; SCHWEIZ; DA. 1975; VOL. 48; NO 1; PP. 75; (SCHWEIZ. GES. GENET. JAHRESVERSAMML. ZUSAMMENFASSUNGEN REFRATE; LAUSANNE; 1974)Conference Paper

ATTITUDE PRATIQUE FACE A L'HYPERTENSION ARTERIELLE DE L'ENFANTGUIGNARD JP; DORNER F; JOTTERAND M et al.1980; REV. MED. SUISSE ROMANDE; CHE; DA. 1980; VOL. 100; NO 3; PP. 213-219; BIBL. 7 REF.Article

Effect of conditioned medium, nutritive elements and mitotic synchronization on the accuracy of the cytogenetic analysis in patients with chronic myeloid leukemia at diagnosis and during α-interferon therapyCASTAGNE, C; MÜHLEMATTER, D; MARTINET, D et al.Cancer genetics and cytogenetics. 1999, Vol 109, Num 2, pp 166-171, issn 0165-4608Article

Detection of 16 p deletions by FISH in patients with inv(16) or t(16;16) and acute myeloid leukemia (AML)MARTINET, D; MÜHLEMATTER, D; LEEMAN, M et al.Leukemia. 1997, Vol 11, Num 7, pp 964-970, issn 0887-6924Article

Hybridation in situ fluorescente (FISH), un complément à l'analyse cytogénétique des hemopathies malignes = Fluorescence in situ hybridization (FISH), an additional technique to cytogentic analysis of malignant hemopathiesMÜHLEMATTER, D; CASTAGNE, C; BEYER, V et al.Revue médicale de la Suisse romande. 2000, Vol 120, Num 5, pp 393-400, issn 0035-3655Article

Dicentric translocation (9;12) presenting as refractory Philadelphia chromosome-positive acute B-cell lymphoblastic leukemiaBARGETZI, M. J; MÜHLEMATTER, D; TICHELLI, A et al.Cancer genetics and cytogenetics. 1999, Vol 113, Num 1, pp 90-92, issn 0165-4608Article

CD34/QBEND10 immunostaining in bone marrow biopsies : an additional parameter for the diagnosis and classification of myelodysplastic syndromesBAUR, A. S; MEUGE-MORAW, C; SCHMIDT, P.-M et al.European journal of haematology. 2000, Vol 64, Num 2, pp 71-79, issn 0902-4441Article

A novel BCR-ABL transcript e2a2 in a chronic myelogenous leukaemia patient with a duplicated Ph-chromosome and monosomy 7LEIBUNDGUT, E. O; JOTTERAND, M; RIGAMONTI, V et al.British journal of haematology. 1999, Vol 106, Num 4, pp 1041-1044, issn 0007-1048Article

Identification of a novel imatinib responsive KIF5B-PDGFRA fusion gene following screening for PDGFRA overexpression in patients with hypereosinophiliaSCORE, J; CURTIS, C; WAGHORN, K et al.Leukemia. 2006, Vol 20, Num 5, pp 827-832, issn 0887-6924, 6 p.Article

Systemic mastocytosis with associated myeloproliferative disease and precursor B lymphoblastic leukaemia with t(13;13)(q12;q22) involving FLT3TZANKOV, A; SOTLAR, K; MUHLEMATTER, D et al.Journal of clinical pathology. 2008, Vol 61, Num 8, pp 958-961, issn 0021-9746, 4 p.Article

Combination of broad molecular screening and cytogenetic analysis for genetic risk assignment and diagnosis in patients with acute leukemiaMEYER-MONARD, S; PARLIER, V; TICHELLI, A et al.Leukemia. 2006, Vol 20, Num 2, pp 247-253, issn 0887-6924, 7 p.Article

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