A CASE OF MULTIPLE SKELETAL ANOMALIES, ECTODERMAL DYSPLASIA, AND SEVERE GROWTH AND MENTAL RETARDATIONSCHINZEL A.1980; HELV. PAEDIATR. ACTA; CHE; DA. 1980; VOL. 35; NO 3; PP. 243-251; ABS. GER/FRE; BIBL. 7 REF.Article

POSSIBLE TRISOMY 1Q25->1Q32 IN A MALFORMED GIRL WITH A DE NOVO INSERTION IN 1QSCHINZEL A.1979; HUM. GENET.; DEU; DA. 1979; VOL. 49; NO 2; PP. 167-173; BIBL. 4 REF.Article

AUTOSOMAL CHROMOSOME ABERRATIONS. A REVIEW OF THE CLINICAL SYNDROMES CAUSED BY STRUCTURAL CHROMOSOME ABERRATIONS, MOSAIC-TRISOMIES 8 AND 9, AND TRIPLOIDY.SCHINZEL A.1976; ERGEBN. INNEREN MED. KINDERHEILKDE; DTSCH.; DA. 1976; VOL. 38; PP. 37-94; BIBL. 9 P. 1/2Article

AN APPLICATION OF HILBERT'S IRREDUCIBILITY THEOREM TO DIOPHANTINE EQUATIONSSCHINZEL A.1982; ACTA ARITH.; ISSN 0065-1036; POL; DA. 1982; VOL. 41; NO 2; PP. 203-211; BIBL. 3 REF.Article

TRISOMY 9 P, A CHROMOSOME ABERRATION WITH DISTINCT RADIOLOGIC FINDINGSSCHINZEL A.1979; RADIOLOGY; USA; DA. 1979; VOL. 130; NO 1; PP. 125-133; BIBL. 37 REF.Article

FETALES HYDANTOIN-SYNDROM BEI GESCHWISTERN = SYNDROME HYDANTOINIQUE FOETAL DANS UNE FRATRIESCHINZEL A.1979; SCHWEIZ. MED. WSCHR.; CHE; DA. 1979; VOL. 109; NO 3; PP. 68-72; ABS. ENG; BIBL. 12 REF.Article

FOUR PATIENTS INCLUDING TWO SISTERS WITH THE ACROCALLOSAL SYNDROME (AGENESIS OF THE CORPUS CALLOSUM IN COMBINATION WITH PREAXIAL HEXADACTYLY)SCHINZEL A.1982; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1982; VOL. 62; NO 4; PP. 382; BIBL. 3 REF.Article

TRISOMY 20PTER -> Q11 IN A MALFORMED BOY FROM A T(13;20)(P11;Q11) TRANSLOCATION-CARRIER MOTHERSCHINZEL A.1980; HUM. GENET.; DEU; DA. 1980; VOL. 53; NO 2; PP. 169-172; BIBL. 9 REF.Article

AUTOSOMALE CHROMOSOMENABERRATIONEN = ABERRATIONS AUTOSOMIQUESSCHINZEL A.1979; ARCH. GENET.; CHE; DA. 1979; VOL. 52; NO 1-2; 204 P.; ABS. ENG; BIBL. 53 REF.Serial Issue

POSTAXIAL POLYDACTYLY, HALLUX DUPLICATION, ABSENCE OF CORPUS CALLOSUM, MACRENCEPHALY AND SEVERE MENTAL RETARDATION: A NEW SYNDROME.SCHINZEL A.1979; HELV. PAEDIATR. ACTA; CHE; DA. 1979; VOL. 34; NO 2; PP. 141-146; ABS. GER/FRE; BIBL. 2 REF.Article

EDITORIAL COMMENT: ACROCALLOSAL SYNDROMESCHINZEL A.1982; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1982; VOL. 12; NO 2; PP. 201-203; BIBL. 11 REF.Article

THE COFFIN-SIRIS SYNDROMESCHINZEL A.1979; ACTA PAEDIATR. SCAND.; SWE; DA. 1979; VOL. 68; NO 3; PP. 449-452; BIBL. 6 REF.Article

DOES FULL MONOSOMY 21 EXIST. A COMMENT TO THE PAPER: A MALE INFANT WITH MONOSOMY 21 BY Y. KANEKO, T. IKEUCHI, M. SASAKI, Y. SATAKE AND S. KUWAJIMA.SCHINZEL A.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 32; NO 1; PP. 105-107; BIBL. 6 REF.Article

REDUCIBILITY OF POLYNOMIALSSCHINZEL A.1971; IN: COMPUT. NUMBER THEORY. PROC. 2ND SCI. RES. COUNC. ATLAS SYMP. OXFORD, 1969; LONDON; ACADEMIC PRESS; DA. 1971; PP. 73-75; BIBL. 4 REF.Conference Proceedings

PARTIAL TRISOMY 7 Q AND PROBABLE PARTIAL MONOSOMY OF 5 P IN THE SON OF A MOTHER WITH A RECIPROCAL TRANSLOCATION BETWEEN 5 P AND 7 QSCHINZEL A; TOENZ O.1979; HUM. GENET.; DEU; DA. 1979; VOL. 53; NO 1; PP. 121-124; BIBL. 17 REF.Article

LYMPHOCYTE CHROMOSOME STUDIES IN HUMANS EXPOSED TO CHEMICAL MUTAGENS. THE VALIDITY OF THE METHOD IN 67 PATIENTS UNDER CYTOSTATIC THERAPY.SCHINZEL A; SCHMID W.1976; MUTATION RES.; NETHERL.; DA. 1976; VOL. 40; NO 2; PP. 139-166; BIBL. 1 P. 1/2Article

PARTIELLE DELETION DES KURZEN ARMES EINES CHROMOSOMES 4 (WOLF-SYNDROM). ZWEI NEUE FAELLE = DELETION PARTIELLE DU BRAS COURT D'UN CHROMOSOME 4 (SYNDROME DE WOLF). DEUX NOUVEAUX CASSCHINZEL A; SCHMID W.1972; ARCH. GENET.; SCHWEIZ; DA. 1972; VOL. 45; NO 2; PP. 88-98; ABS. ANGL.; BIBL. 19REF.Serial Issue

The acrocallosal syndrome in first cousins: widening of the spectrum of clinical features and further support for autosomal recessive inheritanceSCHINZEL, A.Journal of medical genetics. 1988, Vol 25, Num 5, pp 332-336, issn 0022-2593Article

Ulnar-mammary syndromeSCHINZEL, A.Journal of medical genetics. 1987, Vol 24, Num 12, pp 778-781, issn 0022-2593Article

INTERSTITIAL DELETION OF THE LONG ARM OF CHROMOSOME 1, DEL-(1)(Q21->Q25) IN A PROFOUNDLY RETARDED 8-YEAR-OLD GIRL WITH MULTIPLE ANOMALIESSCHINZEL A; SCHMID W.1980; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1980; VOL. 18; NO 4; PP. 305-313; BIBL. 8 REF.Article

Isochromosome formation and subsequent fission or short arm deletion and subsequent isochromosome formation ?SCHINZEL, A.Annales de génétique (Paris). 1990, Vol 33, Num 1, pp 60-60, issn 0003-3995, 1 p.Article

Cyclopia and cebocephaly in two newborn infants with unbalanced segregation of a familial translocation rcp (1;7)(q32;q34)SCHINZEL, A.American journal of medical genetics. 1984, Vol 18, Num 1, pp 153-161, issn 0148-7299Article

HALLUX DUPLICATION, POSTAXIAL POLYDACTYLY, ABSENCE OF THE CORPUS CALLOSUM, SEVERE MENTAL RETARDATION, AND ADDITIONAL ANOMALIES IN TWO UNRELATED PATIENTS: A NEW SYNDROMESCHINZEL A; SCHMID W.1980; AMER. J. MED. GENET.; USA; DA. 1980; VOL. 6; NO 3; PP. 241-249; BIBL. 1 REF.Article

LYMPHOCYTE CHROMOSOME STUDIES IN HUMANS EXPOSED TO CHEMICAL MUTAGENS. THE VALIDITY OF THE METHOD IN 67 PATIENTS UNDER CYTOSTATIC THERAPYSCHINZEL A; SCHMID W.1976; MUTATION RES.; NETHERL.; DA. 1976; VOL. 40; NO 2; PP. 139-166; BIBL. 1 P. 1/2Article

ON INTERESTING WALKS IN A GRAPHBROSTOW W; SCHINZEL A.1972; J. STATIST. PHYS.; U.S.A.; DA. 1972; VOL. 4; PP. 103-110; BIBL. 5 REF.Serial Issue