L'ADMINISTRATION RURALE AU CAMBODGE ET SES PROJETS DE REFORMESAY B.1974Thesis

THREE SIBLINGS WITH ATYPICAL MUCOPOLYSACCHARIDOSIS = MUCOPOLYSACCHARIDOSE ATYPIQUE CHEZ TROIS ENFANTS D'UNE MEME FRATRIEALTAY C; SAY B.1973; ACTA PAEDIATR. SCAND.; SUEDE; DA. 1973; VOL. 62; NO 1; PP. 73-76; BIBL. 16 REF.Serial Issue

FAMILIAL TRIGONOCEPHALY ASSOCIATED WITH SHORT STATURE AND DEVELOPMENTAL DELAYSAY B; MEYER J.1981; AM. J. DIS. CHILD. (1960); ISSN 0002-922X; USA; DA. 1981; VOL. 135; NO 8; PP. 711-712; BIBL. 9 REF.Article

CHROMOSOME ABERRATION IN ECTOPIA CORDIS (46, XX, 17Q⁺).SAY B; WILSEY CE.1978; AMER. HEART J.; U.S.A.; DA. 1978; VOL. 95; NO 2; PP. 274-275; BIBL. 1 REF.Article

ALPHA -THALASSEMIA AND BETA -THALASSEMIA IN A TURKISH FAMILY.ALTAY C; SAY B; YETGIN S et al.1977; AMER. J. HEMATOL.; U.S.A.; DA. 1977; VOL. 2; NO 1; PP. 1-15; BIBL. 26 REF.Article

GONADAL DYSGENESIS IN A PATIENT WITH AN X;3 TRANSLOCATION: CASE REPORT AND REVIEWCARPENTER NJ; SAY B; BROWNING D et al.1980; J. MED. GENET.; GBR; DA. 1980; VOL. 17; NO 3; PP. 216-221; BIBL. 49 REF.Article

PATTERN PROFILE ANALYSIS OF THE HAND IN TRICHLORHINOPHALANGEAL SYNDROME.SAY B; BARBER N; POZNANSKI AK et al.1977; PEDIATRICS; U.S.A.; DA. 1977; VOL. 59; NO 1; PP. 123-126; BIBL. 6 REF.Article

CORNEAL OPACITY, MICROPHTHALMIA, MENTAL RETARDATION, MICROCEPHALY AND GENERALIZED MUSCULAR SPASTICITY ASSOCIATED WITH HYPERGLYCINEMIA = OPACITE CORNEENNE, MICROPHTHALMIE, ARRIERATION MENTALE, MICROCEPHALIE ET SPASTICITE MUSCULAIRE GENERALISEE ASSOCIEES A UNE HYPERGLYCINEMIEBALCI S; SAY B; FIRAT T et al.1974; CLIN. GENET.; DANM.; DA. 1974; VOL. 5; NO 1; PP. 36-39; BIBL. 6REF.Article

FREQUENCY OF RED CELL ADENOSINE DEAMINASE AND 6-PHOSPHOGLUCONATE DEHYDROGENASE IN A SAMPLE OF THE TURKISH POPULATION = FREQUENCE DE L'ADENOSINE DESAMINASE ET DE LA 6-PHOSPHOGLUCONATE DESHYDROGENASE ERYTHROCYTAIRES DANS UN ECHANTILLON DE POPULATION TURQUEALTAY C; SAY B; TUNCBILEK E et al.1974; HUM. HERED.; SWITZ.; DA. 1974; VOL. 24; NO 3; PP. 306-308; BIBL. 9REF.Article

A FAMILIAL SYNDROME OF UNUSUAL FACIES ASSOCIATED WITH MALOCCLUSION AND SHORT STATURE = UN SYNDROME FAMILIAL AVEC FACIES INHABITUEL, MALOCCLUSION ET PETITE TAILLESAY B; TUNCBILEK E; PIRNAR T et al.1973; HUMANGENETIK; DTSCH.; DA. 1973; VOL. 18; NO 3; PP. 279-282; BIBL. 2REF.Serial Issue

FAMILIAL GYNECOMASTIA WITHOUT HYPOGONADISMSAY B; CARPENTER N; COLDWELL JG et al.1979; SOUTH. MED. J.; USA; DA. 1979; VOL. 72; NO 10; PP. 1330-1331; BIBL. 2 REF.Article

THE STICKLER SYNDROME (HEREDITARY ARTHRO-OPHTHALMOPATHY).SAY B; BERRY J; BARBER N et al.1977; CLIN. GENET.; DENM.; DA. 1977; VOL. 12; NO 3; PP. 179-182; BIBL. 5 REF.Article

GOODPASTURE'S SYNDROME (PULMONARY HEMOSIDEROSIS WITH NEPHRITIS) = SYNDROME DE GOODPASTURE (HEMOSIDEROSE PULMONAIRE AVEC NEPHRITE)OZSOYLU S; HICSONMEZ G; BERKEL I et al.1976; CLIN. PEDIATR.; U.S.A.; DA. 1976; VOL. 15; NO 4; PP. 358-360; BIBL. 16 REF.Article

A NEW DOMINANTLY INHERITED SYNDROME OF CLEFT PALATE = UN NOUVEAU SYNDROME DOMINANT DE DIVISION PALATINESAY B; BARBER DH; HOBBS J et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 26; NO 3; PP. 267-269; BIBL. 3REF.Article

AN UNUSUAL CHROMOSOMAL ABERRATION IN A CASE OF CHEDIAK-HIGASHI SYNDROME = UNE ABERRATION CHROMOSOMIQUE INHABITUELLE DANS UN CAS DU SYNDROME DE CHEDIAK-HIGASHISAY B; TUNCBILEK E; YAMAK B et al.1970; J. MED. GENET.; G.B.; DA. 1970; VOL. 7; NO 4; PP. 417-421; BIBL. 25REF.Serial Issue

Current approaches to punctuation in computational linguistics = Approches récentes de la ponctuation en linguistique informatiqueSAY, B; AKMAN, V.Computers and the humanities. 1996, Vol 30, Num 6, pp 457-469, issn 0010-4817Article

AGENESIS OF THE LUNG ASSOCIATED WITH A CHROMOSOME ABNORMALITY (46,XX,2P+)SAY B; CARPENTER NJ; GIACOIA G et al.1980; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1980; VOL. 17; NO 6; PP. 477-478; BIBL. 6 REF.Article

NITROBLUE TETRAZOLIUM TEST IN CHILDREN WITH MALNUTRITION = LE TEST AU NITROBLUE TETRAZOLIUM CHEZ LES ENFANTS SOUFFRANT DE MALNUTRITIONALTAY C; SAY B; DOGRAMACI N et al.1972; J. PEDIATR.; U.S.A.; DA. 1972; VOL. 81; NO 2; PP. 392-393; BIBL. 9REF.Serial Issue

Spondylocostal dysplasia and neural tube defectsGIACOIA, G. P; SAY, B.Journal of medical genetics. 1991, Vol 28, Num 1, pp 51-53, issn 0022-2593, 3 p.Article

AN INFANT WITH RING 17 CHROMOSOME AND UNUSUAL DERMATOGLYPHS: A NEW SYNDROME .CARPENTER NJ; LEICHTMAN LG; STAMPER S et al.1981; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1981; VOL. 18; NO 3; PP. 234-236; BIBL. 7 REF.Article

A CONDITION RESEMBLING CONGENITAL HYPOPLASTIC ANEMIA OCCURRING IN A MOTHER AND SONMCFARLAND G; SAY B; CARPENTER NJ et al.1982; CLINICAL PEDIATRICS; ISSN 0009-9228; USA; DA. 1982; VOL. 21; NO 12; PP. 755-756; BIBL. 7 REF.Article

DOMINANT CONGENITAL COXA VARASAY B; TAYSI K; PIRNAR T et al.1974; J. BONE JOINT SURG., BRIT. ED.; G.B.; DA. 1974; VOL. 56; NO 1; PP. 78-85; BIBL. 7REF.Article

Cloverleaf skull associated with unusual skeletal anomaliesSAY, B; POZNANSKI, A. K.Pediatric radiology. 1987, Vol 17, Num 2, pp 93-96, issn 0301-0449Article

THE RADIAL DYSPLASIA/IMPERFORATE ANUS/VERTEBRAL ANOMALIES SYNDROME (THE VATER ASSOCIATION): DEVELOPMENTAL ASPECTS AND EYE FINDING.GREENBERG D; SAY B; HARRIS R et al.1977; ACTA PAEDIATR. SCAND.; SUEDE; DA. 1977; VOL. 66; NO 2; PP. 233-235; BIBL. 8 REF.Article

FAMILIAL TRANSLOCATION (3P 15P) WITH PARTIAL TRISOMY FOR THE UPPER ARM OF CHROMOSOME 3 IN TWO SIBS.SAY B; BARBER N; BOBROW M et al.1976; J. PEDIATR.; U.S.A.; DA. 1976; VOL. 88; NO 3; PP. 447-450; BIBL. 3 REF.Article