ACNP - Italian Periodicals Catalogue

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Results: 1-13 |

Results: 13

CYTOGENETIC FINDINGS IN 30 LUNG-CARCINOMA PATIENTS

Authors: BERKERKARAUZUM S LULECI G OZBILIM G ERDOGAN A KUZUCU A DEMIRCAN A

Citation: S. Berkerkarauzum et al., CYTOGENETIC FINDINGS IN 30 LUNG-CARCINOMA PATIENTS, Cancer genetics and cytogenetics, 100(2), 1998, pp. 114-123

CYTOGENETIC STUDY IN 102 INFERTILE MEN

Authors: GUNDUZ G LULECI G BAYKARA M

Citation: G. Gunduz et al., CYTOGENETIC STUDY IN 102 INFERTILE MEN, Urologia internationalis, 61(1), 1998, pp. 32-34

A NEW-TYPE FAMILIAL TRANSLOCATION

Authors: LULECI G KESER I BAYSAL C

Citation: G. Luleci et al., A NEW-TYPE FAMILIAL TRANSLOCATION, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 247-247

DE-NOVO DUBLICATION FOR 2Q35-]QTER IN A CHILD

Authors: LULECI G KARAMAN B KARAUZUM SB TACOY S ACAR G

Citation: G. Luleci et al., DE-NOVO DUBLICATION FOR 2Q35-]QTER IN A CHILD, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 248-248

CYTOGENETIC FINDINGS IN 30 LUNG-CARCINOMA PATIENTS

Authors: BERKERKARAUZUM S LULECI G OZBILIM G ERDOGAN A KUZUCU A DEMIRCAN A

Citation: S. Berkerkarauzum et al., CYTOGENETIC FINDINGS IN 30 LUNG-CARCINOMA PATIENTS, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 354-354

GERMLINE HMSH2 AND HMLH1 GENE-MUTATIONS IN INCOMPLETE HNPCC FAMILIES

Authors: WANG Q DESSEIGNE F LASSET C SAURIN JC NAVARRO C YAGCI T KESER I BAGCI H LULECI G GELEN T CHAYVIALLE JA PUISIEUX A OZTURK M

Citation: Q. Wang et al., GERMLINE HMSH2 AND HMLH1 GENE-MUTATIONS IN INCOMPLETE HNPCC FAMILIES, International journal of cancer, 73(6), 1997, pp. 831-836

BLOOMS SYNDROME IN A TURKISH INDIVIDUAL

Authors: YILMAZ E ALPSOY E LULECI G BAGCI G YILMAZ GG CETIN L BASARAN E

Citation: E. Yilmaz et al., BLOOMS SYNDROME IN A TURKISH INDIVIDUAL, Clinical genetics, 49(6), 1996, pp. 314-315

PREMATURE CENTROMERE DIVISION IN 3 UNRELATED FAMILIES

Authors: KESER I LULECI G GUNDUZ G

Citation: I. Keser et al., PREMATURE CENTROMERE DIVISION IN 3 UNRELATED FAMILIES, Annales de genetique, 39(2), 1996, pp. 87-90

NORMAL PHENOTYPE WITH MATERNAL ISODISOMY IN A FEMALE WITH 2 ISOCHROMOSOMES - I(2P) AND I(2Q)

Authors: BERNASCONI F KARAGUZEL A CELEP F KESER I LULECI G DUTLY F SCHINZEL AA

Citation: F. Bernasconi et al., NORMAL PHENOTYPE WITH MATERNAL ISODISOMY IN A FEMALE WITH 2 ISOCHROMOSOMES - I(2P) AND I(2Q), American journal of human genetics, 59(5), 1996, pp. 1114-1118

A SOMATIC ORIGIN OF HOMOLOGOUS ROBERTSONIAN TRANSLOCATIONS AND ISOCHROMOSOMES

Authors: ROBINSON WP BERNASCONI F BASARAN S YUKSELAPAK M NERI G SERVILLE F BALICEK P HALUZA R FARAH LMS LULECI G SCHINZEL AA

Citation: Wp. Robinson et al., A SOMATIC ORIGIN OF HOMOLOGOUS ROBERTSONIAN TRANSLOCATIONS AND ISOCHROMOSOMES, American journal of human genetics, 54(2), 1994, pp. 290-302

MONOSOMY 7 MYELODYSPLASIA IN CHILDHOOD - 2 CASE-REPORTS

Authors: YESILIPEK MA LULECI G VELIPASAOGLU S BERKER S YEGIN O

Citation: Ma. Yesilipek et al., MONOSOMY 7 MYELODYSPLASIA IN CHILDHOOD - 2 CASE-REPORTS, Acta haematologica, 92(1), 1994, pp. 36-38

CALCIFICATION OF BASAL GANGLIA ASSOCIATED WITH PONTINE CALCIFICATION IN 4 CASES - A RADIOLOGIC AND GENETIC-STUDY

Authors: NADERI S COLAKOGLU Z LULECI G

Citation: S. Naderi et al., CALCIFICATION OF BASAL GANGLIA ASSOCIATED WITH PONTINE CALCIFICATION IN 4 CASES - A RADIOLOGIC AND GENETIC-STUDY, Clinical neurology and neurosurgery, 95(2), 1993, pp. 155-157

A CASE OF JUVENILE CHRONIC MYELOID-LEUKEMIA WITH XX XXX MOSAICISM/

Authors: YESILIPEK MA LULECI G OYGUR N BERKER S YEGIN O

Citation: Ma. Yesilipek et al., A CASE OF JUVENILE CHRONIC MYELOID-LEUKEMIA WITH XX XXX MOSAICISM/, Turkish Journal of Pediatrics, 34(4), 1992, pp. 251-254

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