RASSEGNA DI SETTE CASI DI PATOLOGIA AUTOSOMICA DI PUI RARO RISCONTRO: TRISOMIE 9P, MONOSOMIE 18Q, ANNEAU 21, TRISOMIE 6P, TRISOMIE 2Q, TRANSLOCATION 1;21 = REVUE DE 7 CAS DE PATHOLOGIE AUTOSOMIQUE RARE: TRISOMIE 9P, MONOSOMIE 18Q, ANNEAU 21, TRISOMIE 6P, TRISOMIE 2Q, TRANSLOCATION 1:21FIORETTI G; PAGANO L; RENDA S et al.1980; MINERVA PEDIATR.; ISSN 0026-4946; ITA; DA. 1980; VOL. 32; NO 12; PP. 807-814; ABS. ENG; BIBL. 4 REF.Article

EFFECT OF BACTERIAL ENDOTOXIN ON LYSOSOMAL ENZYME ACTIVITIES OF NORMAL AND MUCOLIPIDOSIS III FIBROBLASTSDI NATALE P; STABILE M; RONSISVALLE L et al.1981; BIOMEDICINE; FRA; DA. 1981; VOL. 35; NO 2; PP. 46-49; ABS. FRE; BIBL. 30 REF.Article

A AND B POSTAXIAL POLYDACTYLY IN TWO MEMBERS OF THE SAME FAMILYVENTRUTO V; THEO G; CELONA A et al.1980; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1980; VOL. 18; NO 5; PP. 342-347; BIBL. 5 REF.Article

STUDIO DI UNA FAMIGLIA CON FEMMINILIZZAZIONE TESTICOLARE. QUATTRO SOGGETTI APPARTENENTI A 3 SUCCESSIVE GENERAZIONI. = ETUDE D'UNE FAMILLE AVEC FEMINISATION TESTICULAIRE. QUATRE SUJETS APPARTENANT A 3 GENERATIONS SUCCESSIVESSTABILE M; DI CESARE D; ANNIBALLO R et al.1978; MINERVA PEDIATR.; ITAL.; DA. 1978; VOL. 30; NO 8; PP. 663-668; ABS. ANGL.; BIBL. 8 REF.Article

T(21Q21Q)/R(T(21Q21P)) MOSAIC IN TWO UNRELATED PATIENTS WITH MILD STIGMATA OF DOWN'S SYNDROMEDALLAPICCOLA B; BIANCO I; BRINCHI V et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 1; PP. 56-58; ABS. ENG; BIBL. 4 REF.Article

A CASE OF EDWARD'S SYNDROME WITH PSEUDODICENTRIC ISOCHROMOSOME 18: 46,XY,I DIC(18) (P11:P11)FIORETTI G; STABILE M; PAGANO L et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 2; PP. 116-118; ABS. FRE; BIBL. 13 REF.Article

SU UNA OSSERVAZIONE DI SINDROME DI POLAND: BRACHISINDATTILIA CON APLASIA IPSILATERALE DEL MUSCOLO GRANDE PETTORALE = SUR UNE OBSERVATION DE SYNDROME DE POLAND: BRACHYSYNDACTYLIE AVEC APLASIE IPSILATERALE DU MUSCLE GRAND PECTORALSTABILE M; PISCIOTTA R; CAVALIERE ML et al.1980; MINERVA PEDIATR.; ISSN 0026-4946; ITA; DA. 1980; VOL. 32; NO 11; PP. 759-762; ABS. ENG; BIBL. 7 REF.Article

The Changing Role of Government in Financing Health Care : An International Perspective = L'évolution du rôle du gouvernement dans le financement des soins de santé : une perspective internationaleSTABILE, M; THOMSON, S.2013, 62 p.Report

VALIDATION OF THE SOIL LINE TRANSFORMATION TECHNIQUESTABILE, M. C. C; SEARCY, S. W.Transactions of the ASABE (Print). 2009, Vol 52, Num 2, pp 633-640, issn 2151-0032, 8 p.Article

Hydrops foetalis caused by hepatic haemangiomaALBANO, G; PUGLIESE, A; STABILE, M et al.Acta paediatrica (Oslo). 1998, Vol 87, Num 12, pp 1307-1309, issn 0803-5253Article

Do Stimulant Medications Improve Educational and Behavioral Outcomes for Children with ADHD ? = Les médicaments stimulants améliorent-ils les performances scolaires et le comportement des enfants atteints de TDHD ?CURRIE, J; STABILE, M; JONES, L.E et al.2013, 30 p.Report

A case of suspected teratogenic holoprosencephalySTABILE, M; BIANCO, A; IANNUZZI, S et al.Journal of medical genetics. 1985, Vol 22, Num 2, pp 147-149, issn 0022-2593Article

Child health and young adult outcomes = Etat de santé durant l'enfance et impact sur le jeune adulteCURRIE, J; STABILE, M; MANIVONG, P et al.2008, 38 p.Book

Abnormal B.A.E.P. in a family with Moebius syndrome: evidence for supranuclear lesionSTABILE, M; CAVALIERE, M. L; SCARANO, G et al.Clinical genetics. 1984, Vol 25, Num 5, pp 459-463, issn 0009-9163Article

Fertility in a i(Xq) Klinefelter patient : importance of XIST expression level determined by qRT-PCR in ruling out Klinefelter cryptic mosaicism as cause of oligozoospermiaSTABILE, M; ANGELINO, T; CAIAZZO, F et al.Molecular human reproduction. 2008, Vol 14, Num 11-12, pp 635-640, issn 1360-9947, 6 p.Article

Multiple endocrine neoplasia type 2 (Sipplés syndrome): clinical and cytogenetic analysis of a kindredZATTERALE, A; STABILE, M; NUNZIATA, V et al.Journal of medical genetics. 1984, Vol 21, Num 2, pp 108-111, issn 0022-2593Article

Prune belly appearance in a Turner subjectSAVANELLI, A; ORFEO, L; STABILE, M et al.Journal of medical genetics. 1986, Vol 23, Num 1, pp 92-93, issn 0022-2593Article

Prenatal ultrasound diagnosis of macroglossia in the Wiedemann-Beckwith syndromeCOBELLIS, G; IANNOTO, P; STABILE, M et al.Prenatal diagnosis. 1988, Vol 8, Num 1, pp 79-81, issn 0197-3851Article

Study of a form of pulverulent cataract in a large kindredSTABILE, M; AMORIELLO, A; CAPOBIANCO, S et al.Journal of medical genetics. 1983, Vol 20, Num 6, pp 419-421, issn 0022-2593Article

Seckel syndrome : report of three sibships with the type I primordial dwarfism possible linkage with HLA locusSTOPPOLONI, G; STABILE, M; RINALDI, M. M et al.Annales de génétique (Paris). 1992, Vol 35, Num 4, pp 213-216, issn 0003-3995Article

Multiple skeletal familial abnormalities associated with balanced reciprocal translocation 2; 8 (932; p13)VENTRUTO, V; PISCIOTTA, R; RENDA, S et al.American journal of medical genetics. 1983, Vol 16, Num 4, pp 589-594, issn 0148-7299Article

(7R, 8S, 10bR)-7,8-Dihydroxy-1,5,6,7,8,9,-10.10b-octahydro-3H-1,3-oxazolo[4,5-a]i so-quinolin-3-oneABBOUD, K. A; BUTORA, G; FEARNLEY, S. P et al.Acta crystallographica. Section C, Crystal structure communications. 1998, Vol 54, pp 1162-1164, issn 0108-2701, 8Article

Supplemental oxygen and exercise performance in patients with cystic fibrosis with severe pulmonary diseaseMARCUS, C. L; BADER, D; STABILE, M. W et al.Chest. 1992, Vol 101, Num 1, pp 52-57, issn 0012-3692Article

Childhood sequelae of infant lung disease: exercise and pulmonary function abnormalities after bronchopulmonary dysplasiaBADER, D; RAMOS, A. D; LEW, C. D et al.The Journal of pediatrics. 1987, Vol 110, Num 5, pp 693-699, issn 0022-3476Article

Cytogenetic study of a cell line of human penile cancerGENTILE, G; GIRAIDO, G; STABILE, M et al.Annales de génétique (Paris). 1987, Vol 30, Num 3, pp 164-169, issn 0003-3995Article