UNEXPECTED ENCOUNTERS IN CYTOGENETICS: REPEATED ABORTIONS AND PARENTAL SEX CHROMOSOME MOSAICISM MAY INDICATE RISK OF NONDISJUNCTIONHECHT F.1982; AM. J. HUM. GENET.; ISSN 0002-9297; USA; DA. 1982; VOL. 34; NO 3; PP. 514-516; BIBL. 7 REF.Article

OCCASIONAL COMMENT: GENENTECH AND GEORGE HARDYHECHT F.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 9; NO 3; PP. 261-262Article

DER PALAEOZOISCHE UNTERBAU LIBYENS (LE SUBSTRATUM PALEOZOIQUE DE LA LIBYE).HECHT F.1968; Z. DTSCH. GEOL. GESELLSCH.; DEU; 1968(12), VOL. 117, NUM. 2-3Miscellaneous

LETTER TO THE EDITOR: OBSERVATIONS ON THE NATURAL HISTORY OF 49,XXXXY INDIVIDUALSHECHT F.1982; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1982; VOL. 13; NO 3; PP. 335-336Article

TEACHING MEDICAL GENETICS AND ALICE IN WONDERLANDHECHT F.1981; AM. J. HUM. GENET.; ISSN 0002-9297; USA; DA. 1981; VOL. 33; NO 1; PP. 138-139; BIBL. 2 REF.Article

CONSTRUCTION D'UNE BASE DE FONCTIONS P₁ NON CONFORME A DIVERGENCE NULLE DANS R³HECHT F.1981; R.A.I.R.O. ANAL. NUMER.; ISSN 0399-0516; FRA; DA. 1981; VOL. 15; NO 2; PP. 119-150; ABS. ENG; BIBL. 14 REF.Article

Genetic linkage and physical mapping of a cancer gene : ataxia-telangiectasiaHECHT, F.Cancer genetics and cytogenetics. 1990, Vol 46, Num 1, pp 133-134, issn 0165-4608Article

TORT LIABILITY IN GENETIC DIAGNOSIS AND GENETIC COUNSELINGBURI CE; HECHT F.1982; AM. J. HUM. GENET.; ISSN 0002-9297; USA; DA. 1982; VOL. 34; NO 2; PP. 353-356; BIBL. 12 REF.Article

RADIOCHEMISCHE VERSUCHE ZUR OPTIMIERUNG DER EXTRAKTIONSCHROMATOGRAPHIE MIT POLYTRIFLUORMONOCHLORAETHYLEN (VOLTALEF) ALS TRAEGER = ETUDE RADIOCHIMIQUE DE L'OPTIMALISATION DE LA CHROMATOGRAPHIE D'EXTRACTION AVEC COMME SUPPORT LE POLYTRIFLUOROMONOCHLORETHYLENE (VOLTALEF)BECKER R; HECHT F.1973; MIKROCHIM. ACTA; AUSTR.; DA. 1973; NO 4; PP. 625-640; ABS. ANGL.; BIBL. 1 P.Serial Issue

Rare and polymorphic fragile sites and cancerHECHT, F.Cancer genetics and cytogenetics. 1988, Vol 34, Num 2, pp 195-199, issn 0165-4608Article

Bes, aesop and morgante : reflections of achondroplasiaHECHT, F.Clinical genetics. 1990, Vol 37, Num 4, pp 279-282, issn 0009-9163Article

Mapping the gene for X-linked lymphoproliferative diseaseHECHT, F.Cancer genetics and cytogenetics. 1990, Vol 47, Num 2, pp 271-272, issn 0165-4608Article

KOSMOCHEMISCHE METEORITENUNTERSUCHUNGEN MITTELS NEUTRONENAKTIVIERUNGSANALYSE. = ETUDES COSMOCHIMIQUES DES METEORITES PAR ACTIVATION NEUTRONIQUE.HECHT F; KIESL W.1971; CHEM. D. ERDE; DDR; 1971, VOL. 30, NUM. 0001-0004, P. 145 A 155Miscellaneous

THE IMPORTANCE OF BEING A FRAGILE SITEHECHT F; KAISER MCCAW B.1979; AMER. J. HUM. GENET.; USA; DA. 1979; VOL. 31; NO 2; PP. 223-225; BIBL. 11 REF.Article

INDUCING FRAGILE SITES TO EXPRESS THEMSELVESHECHT F; KAISER MCCAW B.1980; AMER. J. HUM. GENET.; USA; DA. 1980; VOL. 32; NO 4; PP. 626-627; BIBL. 7 REF.Article

MARA AND BENOMI BUCK: FAMILIAL MENTAL RETARDATION IN COLONIAL JAMESTOWNHECHT I. W. D; HECHT F.JOURNAL OF THE HISTORY OF MEDICINE AND ALLIED SCIENCES. 1973, Vol 28, Num 2, pp 171-176Article

INCONTINENTIA PIGMENTI IN ARIZONA INDIANS INCLUDING TRANSMISSION FROM MOTHER TO SON INCONSISTENT WITH THE HALF CHROMATID MUTATION MODELHECHT F; KAISER HECHT B; AUSTIN WJ et al.1982; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1982; VOL. 21; NO 5; PP. 293-296; BIBL. 8 REF.Article

THE FRAGILE X CHROMOSOME. CURRENT METHODSHECHT F; JACKY PB; SUTHERLAND GR et al.1982; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1982; VOL. 11; NO 4; PP. 489-495Article

INHERITANCE OF GIANT PIGMENTED HAIRY NEVUS OF THE SCALPHECHT F; LACANNE KM; CARROLL DB et al.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 9; NO 2; PP. 177-178; BIBL. 3 REF.Article

ACTIVATION ANALYTICAL DETERMINATION OF ELEMENTS IN METEORITES,2.SCHAUDY R; KIESL W; HECHT F et al.1968; CHEM. GEOL.; NLD; 1968(12), VOL. 3, NUM. 0004, P. 307 A 312Miscellaneous

THE USE OF SEQUENTIAL SILVER AND QUINACRINE STAINING TO DETERMINE THE PARENTAL ORIGIN AND BREAKPOINTS OF A RING-22 HUMAN CHROMOSOMEFOWLER G; KAISER MCCAW B; HECHT F et al.1980; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1980; VOL. 18; NO 4; PP. 274-279; BIBL. 9 REF.Article

AMNIOCYTE CLONES FOR PRENATAL CYTOGENETICSHECHT F; PEAKMAN DC; KAISER MCCAW B et al.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 10; NO 1; PP. 51-54; BIBL. 5 REF.Article

ARE BALANCED TRANSLOCATIONS REALLY BALANCED. PRELIMINARY CYTOGENETIC EVIDENCE FOR POSITION EFFECT IN MANHECHT F; KAISER MCCAW B; SHIVANAND PATIL et al.1978; BIRTH DEFECTS ORIGIN. ARTICLE SER.; USA; DA. 1978; VOL. 14; NO 6C; PP. 281-286; BIBL. 7 REF.Article

ESTIMATING DISTANCES FORM THE CENTROMERE BY MEANS OF BENIGN OVARIAN TERATOMAS IN MAN.OTT J; LINDER D; MCCAW BK et al.1976; ANN. HUM. GENET.; G.B.; DA. 1976; VOL. 40; NO 2; PP. 191-196; BIBL. 19 REF.Article

EXCLUSION GENE MAPPING UTILIZING PATIENTS WITH CHROMOSOME IMBALANCE: THE HL-A SYSTEM AS A PROTOTYPE = LA CARTOGRAPHIE DES GENES PAR EXCLUSION GRACE A DES MALADES PORTEURS D'UN DESEQUILIBRE CHROMOSOMIQUE: UTILISATION DU SYSTEME HL-A COMME PROTOTYPEMAGENIS RE; OVERTON K; WYANDT H et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 27; NO 2; PP. 91-109; BIBL. 2P.1/2Article