PRE-IMPLANTATION EMBRYOS OF CHINESE HAMSTER. II. INCIDENCE AND TYPE OF KARYOTYPE ANOMALIES AFTER TREATMENT OF THE PATERNAL POST-MEIOTIC GERM CELLS WITH AN ALKYLATING MUTAGEN.BINKERT F; SCHMID W.1977; MUTATION RES.; NETHERL.; DA. 1977; VOL. 46; NO 2; PP. 77-86; BIBL. 4 REF.Article

PRE-IMPLANTATION EMBRYOS OF CHINESE HAMSTER. I. INCIDENCE OF KARYOTYPE ANOMALIES IN 226 CONTROL EMBRYOS.BINKERT F; SCHMID W.1977; MUTATION RES.; NETHERL.; DA. 1977; VOL. 46; NO 2; PP. 63-76; BIBL. 1 P. 1/2Article

GRUNDLAGENUNTERSUCHUNGEN ZUM DOMINANTEN LETALTEST BEIM CHINESISCHEN HAMSTER = RECHERCHES FONDAMENTALES DE TESTS DES LETAUX DOMINANTS CHEZ LE HAMSTER CHINOISMAIER P; BINKERT F; SCHMID W et al.1975; ARCH. GENET.; SCHWEIZ; DA. 1975; VOL. 48; NO 1; PP. 72-73; (SCHWEIZ. GES. GENET. JAHRESVERSAMML. ZUSAMMENFASSUNGEN REFRATE; LAUSANNE, 1974)Conference Paper

IMMINENT CARDIAC INSUFFICIENCY IN TERMINAL RENAL FAILURE, AN INDICATION FOR THE USE OF A STRAIGHT ARTERIO-ARTERIAL BUSELMEIER "SHUNT" IN THE PEDIATRIC AGE GROUP.BINKERT F; SCHNEIDER A; SCHUEPBACH P et al.1977; VASA; SUISSE; DA. 1977; VOL. 6; NO 3; PP. 270-273; ABS. ALLEM.; BIBL. 14 REF.Article

Partial trisomy of chromosome 18(pter→q12) following a familial 18;21 translocation rcp(18;21)(q12;q11)BINKERT, F; STRANZINGER, J; SCHINZEL, A et al.Human heredity. 1990, Vol 40, Num 2, pp 81-84, issn 0001-5652Article

Ultrasound screening for chromosomal anomalies in the first trimester of pregnancySAVOLDELLI, G; BINKERT, F; ACHERMANN, J et al.Prenatal diagnosis. 1993, Vol 13, Num 6, pp 513-518, issn 0197-3851Article

Molecular study of 45,X conceptuses : correlation with clinical findingsLORDA-SANCHEZ, I; BINKERT, F; MAECHLER, M et al.American journal of medical genetics. 1992, Vol 42, Num 4, pp 487-490, issn 0148-7299Article

A molecular study of X isochromosomes : parental origin, centromeric structure, and mechanisms of formationLORDA-SANCHEZ, I; BINKERT, F; MAECHLER, M et al.American journal of human genetics. 1991, Vol 49, Num 5, pp 1034-1040, issn 0002-9297Article

Reduced recombination and paternal age effect in Klinefelter syndromeLORDA-SANCHEZ, I; BINKERT, F; MAECHLER, M et al.Human genetics. 1992, Vol 89, Num 5, pp 524-530, issn 0340-6717Article

Penoscrotal hypospadias and coarctation of the aorta with mixed gonadal dysgenesisKONRAD, D; SOSSAI, R; WINKLEHNER, H. L et al.Pediatric surgery international. 2000, Vol 16, Num 3, pp 226-228, issn 0179-0358Article

Multiple congenital anomalies including the Rieger eye malformation in a boy with interstitial deletion of (4)(q25→q27) secondary to a balanced insertion in his normal father : evidence for haplotype insufficiency causing the Rieger malformationSCHINZEL, A; BRECEVIC, L; DUTLY, F et al.Journal of medical genetics. 1997, Vol 34, Num 12, pp 1012-1014, issn 0022-2593Article

Exclusively paternal X chromosomes in a girl with short statureSCHINZEL, A. A; ROBINSON, W. P; BINKERT, F et al.Human genetics. 1993, Vol 92, Num 2, pp 175-178, issn 0340-6717Article

No evidence for a paternal interchromosomal effect from analysis of the origin of nondisjunction in down syndrome patients with concomitant familial chromosome rearrangementsSCHINZEL, A. A; ADELSBERGER, P. A; BINKERT, F et al.American journal of human genetics. 1992, Vol 50, Num 2, pp 288-293, issn 0002-9297Article

Interstitial deletion, del(4)(q12q21.1), owing to de novo unbalanced translocation in a 2 year old girl : further evidence that the piebald trait maps to proximal 4q12SCHINZEL, A; BRAEGGER, C. P; BRECEVIC, L et al.Journal of medical genetics. 1997, Vol 34, Num 8, pp 692-695, issn 0022-2593Article

Intrachromosomal triplication of 15q11-q13SCHINZEL, A. A; BRECEVIC, L; BERNASCONI, F et al.Journal of medical genetics. 1994, Vol 31, Num 10, pp 798-803, issn 0022-2593Article

Parental origin of the supernumerary chromosome in trisomy 18XIE YA-GANG; ROBINSON, W. P; SPIEGEL, R et al.Clinical genetics. 1993, Vol 44, Num 2, pp 57-61, issn 0009-9163Article

Down syndrome due to de novo Robertsonian translocation t(14q;21q) : DNA polymorphism analysis suggests that the origin of the extra 21q is maternalPETERSEN, M. B; ADELSBERGER, P. A; SCHINZEL, A. A et al.American journal of human genetics. 1991, Vol 49, Num 3, pp 529-536, issn 0002-9297Article

A 48,XXY,+21 down syndrome patient with additional paternal X and maternal 21LORDA-SANCHEZ, I; PETERSEN, M. B; BINKERT, F et al.Human genetics. 1991, Vol 87, Num 1, pp 54-56, issn 0340-6717Article

Interstitial deletion of the long term arm of chromosome 18, del(18)(q12.2q21.1) : a report of three cases of an autosomal deletion with a mild phenotypeSCHINZEL, A; BINKERT, F; LILLINGTON, D. M et al.Journal of medical genetics. 1991, Vol 28, Num 5, pp 352-355, issn 0022-2593Article

Kallmann syndrome in a boy with a t(1;10) translocation detected by reverse chromosome paintingSCHINZEL, A; LORDA-SANCHEZ, I; BINKERT, F et al.Journal of medical genetics. 1995, Vol 32, Num 12, pp 957-961, issn 0022-2593Article

Use of short sequence repeat DNA polymorphisms after PCR amplification to detect the parental origin of the additional chromosome 21 in down syndromePETERSEN, M. B; SCHINZEL, A. A; BINKERT, F et al.American journal of human genetics. 1991, Vol 48, Num 1, pp 65-71, issn 0002-9297, 7 p.Article

Parental origin and mechanisms of formation of cytogenetically recognisable de novo direct and inverted duplicationsKOTZOT, D; MARTINEZ, M.-J; GUTKOWSKA, A et al.Journal of medical genetics. 2000, Vol 37, Num 4, pp 281-286, issn 0022-2593Article

Prenatal diagnosis of atypical phenylketonuriaBLAU, N; NIEDERWIESER, A; PONZONE, A et al.Journal of inherited metabolic disease. 1989, Vol 12, pp 295-298, issn 0141-8955, suppl. 2Article

The meiotic stage of nondisjunction in trisomy 21 : determination by using DNA polymorphismsANTONARAKIS, S. E; PETERSEN, M. B; COHEN, M. M et al.American journal of human genetics. 1992, Vol 50, Num 3, pp 544-550, issn 0002-9297Article

DNA polymorphism analysis in families with recurrence of free trisomy 21PANGALOS, C. G; CONOVER TALBOT, C. JR; BINKERT, F et al.American journal of human genetics. 1992, Vol 51, Num 5, pp 1015-1027, issn 0002-9297Article