HYPOGENITALISM IN THE ACROCALLOSAL SYNDROME

[1] AICARDI J, 1969, ARCH FR PEDIATR, V26, P1103

[2] Andermann F., 1972, T AM NEUROL ASS, V97, P242

[3] HYDROLETHALUS SYNDROME - REPORT OF AN APPARENT MILD CASE, LITERATURE-REVIEW, AND DIFFERENTIAL-DIAGNOSIS [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1987, 27 (04): : 935 - 942

[4] BARAITSER M, 1983, CLIN GENET, V24, P257

[5] MEDIAN CLEFT FACE SYNDROME IN ASSOCIATION WITH HYDROCEPHALUS, AGENESIS OF THE CORPUS-CALLOSUM, HOLOPROSENCEPHALY AND CHOANAL ATRESIA [J]. EUROPEAN JOURNAL OF PEDIATRICS, 1987, 146 (03) : 301 - 302

[6] CASTROGAGO M, 1982, REV ESP PEDIATR, V38, P349

[7] THE GREIG CEPHALOPOLYSYNDACTYLY SYNDROME IN A CANADIAN FAMILY [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1982, 13 (03): : 269 - 276

[8] THE GREIG CEPHALOPOLYSYNDACTYLY SYNDROME - REPORT OF A FAMILY AND REVIEW OF THE LITERATURE [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1985, 22 (01): : 59 - 68

[9] PRENATAL-DIAGNOSIS OF A PROBABLE HEREDITARY SYNDROME WITH HOLOPROSENCEPHALY, HYDROCEPHALY, OCTODACTYLY, AND CARDIAC-MALFORMATIONS [J]. EUROPEAN JOURNAL OF PEDIATRICS, 1984, 143 (02) : 155 - 157

[10] IONASESCU V, 1989, AM J MED GENET, V26, P189

[1] AICARDI J, 1969, ARCH FR PEDIATR, V26, P1103

[2] Andermann F., 1972, T AM NEUROL ASS, V97, P242

[3] HYDROLETHALUS SYNDROME - REPORT OF AN APPARENT MILD CASE, LITERATURE-REVIEW, AND DIFFERENTIAL-DIAGNOSIS [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1987, 27 (04): : 935 - 942

[4] BARAITSER M, 1983, CLIN GENET, V24, P257

[5] MEDIAN CLEFT FACE SYNDROME IN ASSOCIATION WITH HYDROCEPHALUS, AGENESIS OF THE CORPUS-CALLOSUM, HOLOPROSENCEPHALY AND CHOANAL ATRESIA [J]. EUROPEAN JOURNAL OF PEDIATRICS, 1987, 146 (03) : 301 - 302

[6] CASTROGAGO M, 1982, REV ESP PEDIATR, V38, P349

[7] THE GREIG CEPHALOPOLYSYNDACTYLY SYNDROME IN A CANADIAN FAMILY [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1982, 13 (03): : 269 - 276

[8] THE GREIG CEPHALOPOLYSYNDACTYLY SYNDROME - REPORT OF A FAMILY AND REVIEW OF THE LITERATURE [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1985, 22 (01): : 59 - 68

[9] PRENATAL-DIAGNOSIS OF A PROBABLE HEREDITARY SYNDROME WITH HOLOPROSENCEPHALY, HYDROCEPHALY, OCTODACTYLY, AND CARDIAC-MALFORMATIONS [J]. EUROPEAN JOURNAL OF PEDIATRICS, 1984, 143 (02) : 155 - 157

[10] IONASESCU V, 1989, AM J MED GENET, V26, P189