A DUPLICATION-DEFICIENCY X CHROMOSOME IN A GIRL WITH SEVERE MENTAL RETARDATIONSACCHI N; DALPRA L; KEHYAYAN E et al.1980; HUM. GENET.; DEU; DA. 1980; VOL. 54; NO 2; PP. 279-281; BIBL. 10 REF.Article

SATELLITE ASSOCIATIONS AND SILVER STAINING IN A CASE OF MULTIPLE G AND D VARIANTSDI LERNIA R; RIVA ML; DALPRA L et al.1980; HUM. GENET.; DEU; DA. 1980; VOL. 53; NO 2; PP. 237-240; BIBL. 12 REF.Article

VARIATIONS OF DNA REPAIR SYNTHESIS AFTER UV IRRADIATION IN PHA STIMULATED LYMPHOCYTESDALPRA L; STEFANINI M; GIULOTTO E et al.1979; HAEMATOLOGICA; ITA; DA. 1979; VOL. 64; NO 1; PP. 31-39; ABS. ITA; BIBL. 17 REF.Article

Chromosomal instability in Incontinentia pigmenti: study of four familiesPALLOTTA, R; DALPRA, L.Annales de génétique (Paris). 1988, Vol 31, Num 1, pp 27-31, issn 0003-3995Article

THE OFFSPRING OF MARRIAGE BETWEEN TWO FIRST COUSINS WITH THE SAME RECIPROCAL TRANSLOCATION T(2; 7) (P11; Q31)SIMONI G; DALPRA L; TERZOLI GL et al.1980; HUM. GENET.; DEU; DA. 1980; VOL. 55; NO 2; PP. 199-202; BIBL. 13 REF.Article

Further delineation of 7p trisomy : Case report and review literaturePALLOTTA, R; DALPRA, L; FUSILLI, P et al.Annales de génétique (Paris). 1996, Vol 39, Num 3, pp 152-158, issn 0003-3995Article

47, XXX CHROMOSOME CONSTITUTION IN A MALEBIGOZZI U; SIMONI G; MONTALI E et al.1980; J. MED. GENET.; GBR; DA. 1980; VOL. 17; NO 1; PP. 62-66; BIBL. 16 REF.Article

RING CHROMOSOME 10 ASSOCIATED WITH MULTIPLE CONGENITAL MALFORMATIONSSIMONI G; ROSSELLA F; DALPRA L et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 51; NO 2; PP. 117-121; BIBL. 8 REF.Article

CYTOGENETIC FINDINGS IN 4952 PRENATAL DIAGNOSES. AN ITALIAN COLLABORATIVE STUDYSIMONI G; FRACCARO M; ARSLANIAN A et al.1982; HUM. GENT.; ISSN 0340-6717; DEU; DA. 1982; VOL. 60; NO 1; PP. 63-68; BIBL. 8 REF.Article

SCE ANALYSIS IN CHILDREN EXPOSED TO LEAD EMISSION FROM A SMELTING PLANTDALPRA L; TIBILETTI MG; NOCERA G et al.1983; MUTATION RESEARCH; ISSN 0027-5107; NLD; DA. 1983; VOL. 120; NO 4; PP. 249-256; BIBL. 1 P.Article

DIFFERENCES IN THE LEVELS OF UV REPAIR AND IN CLINICAL SYMPTOMS IN TWO SIBS AFFECTED BY XERODERMA PIGMENTOSUMSTEFANINI M; KEIJZER W; DALPRA L et al.1980; HUM. GENET.; DEU; DA. 1980; VOL. 54; NO 2; PP. 177-182; BIBL. 16 REF.Article

A WOMAN CARRIER OF TWO APPARENTLY UNRELATED RECIPROCAL TRANSLOCATIONS: PRENATAL DIAGNOSIS OF NORMAL KARYOTYPE IN THE FOETUSSIMONI G; MONTALI E; ROSSELLA F et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 46; NO 2; PP. 159-162; BIBL. 7 REF.Article

INCORPORATION OF (³H) THYMIDINE STIMULATED BY ULTRAVIOLET RADIATION INTO HUMAN FIBROBLAST CULTURESSTEFANINI M; DALPRA L; ZEI G et al.1976; MUTATION RES.; NETHERL.; DA. 1976; VOL. 34; NO 2; PP. 313-325; BIBL. 17 REF.Article

Five cases of prenatally diagnosed sex chromosome mosaicismNOCERA, G; DALPRA, L; TIBILETTI, M. G et al.Prenatal diagnosis. 1985, Vol 5, Num 3, pp 169-174, issn 0197-3851Article

Genotype-phenotype correlation in two sets of monozygotic twins with Williams syndromeCASTORINA, P; SELICORNI, A; BEDESCHI, F et al.American journal of medical genetics. 1997, Vol 69, Num 1, pp 107-111, issn 0148-7299Article

Different phenotypes in two cases of an apparently identical familial (Yq;13p) translocationDONEDA, L; MAGNANI, I; TIBILETTI, M. G et al.Human reproduction (Oxford. Print). 1992, Vol 7, Num 4, pp 495-499, issn 0268-1161Article

The phenotype of partial dup (7q) reconsidered: a report of five new casesFORABOSCO, A; BARONCINI, A; DALPRA, L et al.Clinical genetics. 1988, Vol 34, Num 1, pp 48-59, issn 0009-9163Article

A rare non-heterochromatic 9p+ variant in two amniotic fluid cell culturesARCHIDIACONO, N; PECILE, V; ROCCHI, M et al.Prenatal diagnosis. 1984, Vol 4, Num 3, pp 231-233, issn 0197-3851Article

Morphology and nuclear content in IVF embryosDALPRA, L; TIBILETTI, M. G; CRISTIANI, C et al.Annales de génétique (Paris). 1993, Vol 36, Num 2, pp 100-106, issn 0003-3995Article

Routine chromosome analysis on fetal blood microaliquots obtained at fetoscopySIMONI, G; TIBILETTI, M. G; DALPRA, L et al.Prenatal diagnosis. 1983, Vol 3, Num 3, pp 203-208, issn 0197-3851Article

Influence of intermediate and uninterrupted FMR1 CGG expansions in premature ovarian failure manifestationBODEGA, B; BIONE, S; DALPRA, L et al.Human reproduction (Oxford. Print). 2006, Vol 21, Num 4, pp 952-957, issn 0268-1161, 6 p.Article

19p deletion in recurring leiomyosarcoma lesions from the same patientRIVA, P; DALPRA, L; GUALANDRI, V et al.Cancer genetics and cytogenetics. 2000, Vol 119, Num 2, pp 102-108, issn 0165-4608Article

Characterization of a cytogenetic 17q11.2 deletion in an NF1 patient with a contiguous gene syndromeRIVA, P; CASTORINA, P; MANOUKIAN, S et al.Human genetics. 1996, Vol 98, Num 6, pp 646-650, issn 0340-6717Article

Mutation analysis of the inhibin alpha gene in a cohort of Italian women affected by ovarian failureMAROZZI, A; PORTA, C; VEGETTI, W et al.Human reproduction (Oxford. Print). 2002, Vol 17, Num 7, pp 1741-1745, issn 0268-1161Article

Identification of a small supernumerary marker chromosome, r(2)(p10q11.2), and the problem of determining prognosisVILLA, N; RIVA, P; COLOMBO, D et al.Prenatal diagnosis. 2001, Vol 21, Num 10, pp 801-805, issn 0197-3851Article