RETINOBLASTOMA IN A PATIENT WITH A 13QXP TRANSLOCATION

[1] ALLERDICE PW, 1969, AM J HUM GENET, V21, P499

[2] BENTLEY D, 1975, PEDIATRICS, V56, P131

[3] CZEIZEL A, 1974, HUMANGENETIK, V22, P159

[4] DAY RW, 1963, LANCET, V2, P154

[5] FRASER GR, 1967, CAUSES BLINDNESS CHI, P37

[6] DQ-, MULTIPLE MALFORMATIONS AND RETINOBLASTOMA [J]. HUMANGENETIK, 1970, 10 (04): : 362 - &

[7] 13Q- DELETION SYNDROME [J]. JOURNAL OF MEDICAL GENETICS, 1971, 8 (03) : 351 - &

[8] RETINOBLASTOMA - MODEL OF HEREDITARY FRAGILE CHROMOSOMAL REGIONS [J]. HUMAN HEREDITY, 1975, 25 (01) : 35 - 49

[9] Herrmann J, 1976, Birth Defects Orig Artic Ser, V12, P79

[10] RETINOBLASTOMA AND CHROMOSOME ABNORMALITY [J]. ARCHIVES OF OPHTHALMOLOGY, 1974, 92 (06) : 490 - 493

[1] ALLERDICE PW, 1969, AM J HUM GENET, V21, P499

[2] BENTLEY D, 1975, PEDIATRICS, V56, P131

[3] CZEIZEL A, 1974, HUMANGENETIK, V22, P159

[4] DAY RW, 1963, LANCET, V2, P154

[5] FRASER GR, 1967, CAUSES BLINDNESS CHI, P37

[6] DQ-, MULTIPLE MALFORMATIONS AND RETINOBLASTOMA [J]. HUMANGENETIK, 1970, 10 (04): : 362 - &

[7] 13Q- DELETION SYNDROME [J]. JOURNAL OF MEDICAL GENETICS, 1971, 8 (03) : 351 - &

[8] RETINOBLASTOMA - MODEL OF HEREDITARY FRAGILE CHROMOSOMAL REGIONS [J]. HUMAN HEREDITY, 1975, 25 (01) : 35 - 49

[9] Herrmann J, 1976, Birth Defects Orig Artic Ser, V12, P79

[10] RETINOBLASTOMA AND CHROMOSOME ABNORMALITY [J]. ARCHIVES OF OPHTHALMOLOGY, 1974, 92 (06) : 490 - 493