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Unusual chromosome 20 anomaly arising de novo to give dic(20)qs

Human genetics, 1989-12, Vol.84 (1), p.97-98

1989

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C-band length variability and reproductive wastage

Human genetics, 1987, Vol.75 (1), p.56-61

1987

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Maternal 3:1 disjunction in a tranlocation 9/17

Human genetics, 1986-06, Vol.73 (2), p.188-188

1986

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Infertility associated with two accessory bisatellited chromosomes

Human genetics, 1986-06, Vol.73 (2), p.133-136

1986

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Maternal 3:1 disjunction in a translocation 9/17

Human genetics, 1986-06, Vol.73 (2), p.188-188

1986

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Trisomy 14 by paternal origin

Human genetics, 1984-01, Vol.68 (2), p.193-193

1984

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Is a gene for microcephaly located on chromosome 1?

Human genetics, 1984-01, Vol.67 (2), p.230-232

1984

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Four cases of partial trisomy 4p by preferential segregation in a familial 4p/17q balanced translocation

Human genetics, 1984, Vol.66 (4), p.370-370

1984

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Partial trisomy 18 due to a maternal translocation t(9;18)

Human genetics, 1984-01, Vol.68 (3), p.272-272

1984

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Unusual pericentric inversion inv(9) (p13q11) in a phenotypically normal family

Human genetics, 1983-01, Vol.64 (1), p.100-100

1983

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Trisomy 21: origin of non-disjunction

Human genetics, 1982-01, Vol.62 (4), p.316-320

1982

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A new case of satellited yq chromosome

Human genetics, 1982-01, Vol.61 (3), p.277-277

1982

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An r(22)(p11 leads to q13) in a moderately mentally retarded girl

Human genetics, 1979-10, Vol.51 (2), p.157-162

1979

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Trisomy 10p due to a de novo t(10p;13p)

Human genetics, 1979-01, Vol.46 (2), p.129-134

1979

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Study of human male meiosis. II-Q-banding in pachytene bivalents

Human genetics, 1978-01, Vol.42 (3), p.283-289

1978

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Patau's syndrome and 13q21q translocation

Human genetics, 1978-01, Vol.42 (3), p.327-331

1978

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Partial deletion of 4p16 band in a ring chromosome and Wolf Syndrome

Human genetics, 1978-01, Vol.44 (1), p.105-108

1978

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Study of the human male meiosis. I. G-banding in pachytene bivalents

Human genetics, 1977-11, Vol.39 (2), p.161-168

1977

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Human triploid embryo: cytogenetic and anatomopathologic study

Human genetics, 1977-01, Vol.39 (2), p.251-256

1977

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Ring chromosome 4 and Wolf syndrome

Human genetics, 1977-01, Vol.37 (1), p.87-91

1977

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A new contribution to the study of 22 trisomy

Human genetics, 1975-09, Vol.30 (3), p.265-271

1975

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Unusual chromosome 20 anomaly arising de novo to give dic(20)qs

C-band length variability and reproductive wastage

Maternal 3:1 disjunction in a tranlocation 9/17

Infertility associated with two accessory bisatellited chromosomes

Maternal 3:1 disjunction in a translocation 9/17

Trisomy 14 by paternal origin

Is a gene for microcephaly located on chromosome 1?

Four cases of partial trisomy 4p by preferential segregation in a familial 4p/17q balanced translocation

Partial trisomy 18 due to a maternal translocation t(9;18)

Unusual pericentric inversion inv(9) (p13q11) in a phenotypically normal family

Trisomy 21: origin of non-disjunction

A new case of satellited yq chromosome

An r(22)(p11 leads to q13) in a moderately mentally retarded girl

Trisomy 10p due to a de novo t(10p;13p)

Study of human male meiosis. II-Q-banding in pachytene bivalents

Patau's syndrome and 13q21q translocation

Partial deletion of 4p16 band in a ring chromosome and Wolf Syndrome

Study of the human male meiosis. I. G-banding in pachytene bivalents

Human triploid embryo: cytogenetic and anatomopathologic study

Ring chromosome 4 and Wolf syndrome

A new contribution to the study of 22 trisomy

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