An algorithm for constructing Gröbner and free Schreier bases in free group algebrasROSENMANN, A.Journal of symbolic computation. 1993, Vol 16, Num 6, pp 523-549, issn 0747-7171Article

ECTRODACTYLY, ECTODERMAL DYSPLASIA AND CLEFT PALATE (EEC SYNDROME). REPORT OF A FAMILY AND REVIEW OF THE LITERATUREROSENMANN A; SHAPIRA T; COHEN MM et al.1976; CLIN. GENET.; DENM.; DA. 1976; VOL. 9; NO 3; PP. 347-353; BIBL. 21 REF.Article

SIB RISK OF NEURAL TUBE DEFECT: IS PRENATAL DIAGNOSIS INDICATED IN PREGNANCIES FOLLOWING THE BIRTH OF A HYDROCEPHALIC CHILD.COHEN T; STERN E; ROSENMANN A et al.1979; J. MED. GENET.; GBR; DA. 1979; VOL. 16; NO 1; PP. 14-16; BIBL. 14 REF.Article

PARTIAL TRISOMY 18(Q11->QTER) IN AN INFANT AND ABORTED FETUS RESULTING FROM A BALANCED PATERNAL TRANSLOCATION T(13;18) (Q32;Q11).ROSENMANN A; ISACSON M; COHEN R et al.1978; ANN. GENET.; FR.; DA. 1978; VOL. 21; NO 1; PP. 60-64; ABS. FR.; BIBL. 20 REF.Article

11-DEOXYCORTISOL IN AMNIOTIC FLUID: PRENATAL DIAGNOSIS OF CONGENITAL ADRENAL HYPERPLASIA DUE TO 11BETA -HYDROXYLASE DEFICIENCYSCHUMERT Z; ROSENMANN A; LANDAU H et al.1980; CLIN. ENDOCRINOL.; GBR; DA. 1980; VOL. 12; NO 3; PP. 257-260; BIBL. 9 REF.Article

FAMILIAL EBSTEIN'S ANOMALY.ROSENMANN A; ARAD I; SIMCHA A et al.1976; J. MED. GENET.; G.B.; DA. 1976; VOL. 13; NO 6; PP. 532-534; BIBL. 16 REF.Article

PARTIAL TRISOMY D: A DIAGNOSTIC AND CYTOGENETIC DILEMNA.COHEN MM; ROSENMANN A; DAGAN J et al.1976; J. MED. GENET.; G.B.; DA. 1976; VOL. 13; NO 6; PP. 535-538; BIBL. 11 REF.Article

DICENTRIC X-ISOCHROMOSOME (XQI DIC) AND PERICENTRIC INVERSION OF NO.2 (INV(2)(P15Q21)) IN A PATIENT WITH GONADAL DYSGENESIS = ISOCHROMOSOME X DICENTRIQUE (XQI DIC) ET INVERSION PERICENTRIQUE DU NO 2 (INV(2)(P15Q21)) CHEZ UN MALADE ATTEINT DE DYSGENESIE GONADIQUECOHEN MM; ROSENMANN A; HACHAM ZADEH S et al.1975; CLIN. GENET.; DENM.; DA. 1975; VOL. 8; NO 1; PP. 11-17; BIBL. 16 REF.Article

AN INHERITED TRANSLOCATION T(4;15)(P16;Q22) LEADING TO TWO CASES OF PARTIAL TRISOMY 15COHEN MM; ORNOY A; ROSENMANN A et al.1975; ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 2; PP. 99-103; ABS. FR.; BIBL. 10REF.Article

HISTIDINAEMIA. II: IMPACT; A RETROSPECTIVE STUDYROSENMANN A; SCRIVER CR; CLOW CL et al.1983; JOURNAL OF INHERITED METABOLIC DISEASE; ISSN 0141-8955; GBR; DA. 1983; VOL. 6; NO 2; PP. 54-57; BIBL. 2 P.Article

AMNIOTIC 17-ALPHA HYDROXYPROGESTERONE AND HLA TYPING FOR THE PRENATAL DIAGNOSIS OF 21-ALPHA HYDROXYLASE DEFICIENCY-CONGENITAL ADRENAL HYPERPLASIAROSENMANN A; SCHUMERT Z; THEODOR R et al.1980; AMER. J. MED. GENET.; USA; DA. 1980; VOL. 6; NO 4; PP. 295-300; BIBL. 22 REF.Article

CHROMOSOMES IN FAMILIAL PRIMARY STERILITY AND IN COUPLES WITH RECURRENT ABORTIONS AND STILLBIRTHS.ROSENMANN A; SEGAL S; PALTI Z et al.1977; ISRAEL J. MED. SCI.; ISRAEL; DA. 1977; VOL. 13; NO 11; PP. 1131-1133; BIBL. 13 REF.Article

A LONG UNIDENTIFIABLE EXTRA CHROMOSOMAL SEGMENT - A POSSIBLE DUPLICATION OF HUMAN 7Q.WAHRMAN J; COHEN MM; ROSENMANN A et al.1978; CYTOGENET. CELL GENET.; SWITZ.; DA. 1978; VOL. 20; NO 1-6; PP. 160-168; BIBL. 16 REF.Article

CHROMATIN-POSITIVE KLINEFELTER'S SYNDROME WITH UNDETECTABLE PERIPHERAL FSH LEVELS. = SYNDROME DE KLINEFELTER AVEC CHROMATINE POSITIVE PRESENTANT DES TAUX EFFONDRES DE FSH PERIPHERIQUERABINOWITZ D; COHEN MM; ROSENMANN E et al.1975; AMER. J. MED.; U.S.A.; DA. 1975; VOL. 59; NO 4; PP. 584-590; BIBL. 14 REF.Article

PRENATAL DIAGNOSIS OF 11 BETA -HYDROXYLASE DEFICIENCY CONGENITAL ADRENAL HYPERPLASIAROESLER A; LEIBERMAN E; ROSENMANN A et al.1979; J. CLIN. ENDOCRINOL. METABOL.; USA; DA. 1979; VOL. 49; NO 4; PP. 546-551; BIBL. 40 REF.Article

AMNIOTIC FLUID 3,'3',5'-TRIIODOTHYRONINE IN THE DETECTION OF CONGENITAL HYPOTHYROIDISMLANDAU H; SACK J; FRUCHT H et al.1980; J. CLIN. ENDOCRINOL. METABOL.; USA; DA. 1980; VOL. 50; NO 4; PP. 799-801; BIBL. 9 REF.Article

Chromosomally derived sterile mice have a fertile active XY chromatin conformation but no XY bodyRICHLER, C; ULIEL, E; ROSENMANN, A et al.Chromosoma (Berlin. Print). 1989, Vol 97, Num 6, pp 465-474, issn 0009-5915Article

Under what circumstances is the human XY bivalent tangled? A note on chromosomally-derived sterilityROSENMANN, A; WAHRMAN, J; RICHLER, C et al.Cytogenetics and cell genetics. 1987, Vol 45, Num 1, pp 58-61, issn 0301-0171Article

Meiotic association between the XY chromosomes and unpaired autosomal elements as a cause of human male sterilityROSENMANN, A; WAHRMAN, J; RICHLER, C et al.Cytogenetics and cell genetics. 1985, Vol 39, Num 1, pp 19-29, issn 0301-0171Article

Mutations of the tyrosinase gene in patients with oculocutaneous albinism from various ethnic groups in IsraelGERSHONI-BARUCH, R; ROSENMANN, A; DROETTO, S et al.American journal of human genetics. 1994, Vol 54, Num 4, pp 586-594, issn 0002-9297Article

Persistent Müllerian structures in fertile maleHERSHLAG, A; SPITZ, I. M; HOCHNER-CELNIKIER, D et al.Urology (Ridgewood, NJ). 1986, Vol 28, Num 2, pp 138-141, issn 0090-4295Article

DNA-based carrier detection and prenatal diagnosis of tyrosinase-negative oculocutaneous albinism (OCA1A)FALIK-BORENSTEIN, T. C; HOLMES, S. A; BOROCHOWITZ, Z et al.Prenatal diagnosis. 1995, Vol 15, Num 4, pp 345-349, issn 0197-3851Article

Homozygosity mapping of achromatopsia to chromosome 2 using DNA poolingARBOUR, N. C; ZLOTOGORA, J; KNOWLTON, R. G et al.Human molecular genetics (Print). 1997, Vol 6, Num 5, pp 689-694, issn 0964-6906Article