New case of contiguous gene syndrome at chromosome 8p11.2p12

[1] CONTIGUOUS GENE SYNDROMES DUE TO DELETIONS IN THE DISTAL SHORT ARM OF THE HUMAN X-CHROMOSOME [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (24) : 10001 - 10005

[2] CHILCOTE RR, 1987, BLOOD, V69, P156

[3] CONGENITAL SPHEROCYTOSIS, B19-PARVOVIRUS INFECTION AND INHERITED INTERSTITIAL DELETION OF THE SHORT ARM OF CHROMOSOME-8 [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1991, 78 (02) : 251 - 257

[4] Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome [J]. NATURE GENETICS, 2003, 33 (04) : 463 - 465

[5] Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis [J]. NATURE GENETICS, 1996, 13 (02) : 214 - 218

[6] A GENE DELETED IN KALLMANNS SYNDROME SHARES HOMOLOGY WITH NEURAL CELL-ADHESION AND AXONAL PATH-FINDING MOLECULES [J]. NATURE, 1991, 353 (6344) : 529 - 536

[7] Kallmann FJ, 1944, AM J MENT DEF, V48, P203

[8] LOCALIZATION OF THE SPHEROCYTOSIS GENE TO CHROMOSOME SEGMENT 8P11.22-]8P21.1 [J]. HUMAN GENETICS, 1988, 78 (01) : 94 - 95

[9] HEREDITARY SPHEROCYTOSIS ASSOCIATED WITH DELETION OF HUMAN ERYTHROCYTE ANKYRIN GENE ON CHROMOSOME-8 [J]. NATURE, 1990, 345 (6277) : 736 - 739

[10] HEREDITARY SPHEROCYTIC ANEMIA WITH DELETION OF THE SHORT ARM OF CHROMOSOME-8 [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1995, 58 (03): : 225 - 229

[1] CONTIGUOUS GENE SYNDROMES DUE TO DELETIONS IN THE DISTAL SHORT ARM OF THE HUMAN X-CHROMOSOME [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (24) : 10001 - 10005

[2] CHILCOTE RR, 1987, BLOOD, V69, P156

[3] CONGENITAL SPHEROCYTOSIS, B19-PARVOVIRUS INFECTION AND INHERITED INTERSTITIAL DELETION OF THE SHORT ARM OF CHROMOSOME-8 [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1991, 78 (02) : 251 - 257

[4] Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome [J]. NATURE GENETICS, 2003, 33 (04) : 463 - 465

[5] Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis [J]. NATURE GENETICS, 1996, 13 (02) : 214 - 218

[6] A GENE DELETED IN KALLMANNS SYNDROME SHARES HOMOLOGY WITH NEURAL CELL-ADHESION AND AXONAL PATH-FINDING MOLECULES [J]. NATURE, 1991, 353 (6344) : 529 - 536

[7] Kallmann FJ, 1944, AM J MENT DEF, V48, P203

[8] LOCALIZATION OF THE SPHEROCYTOSIS GENE TO CHROMOSOME SEGMENT 8P11.22-]8P21.1 [J]. HUMAN GENETICS, 1988, 78 (01) : 94 - 95

[9] HEREDITARY SPHEROCYTOSIS ASSOCIATED WITH DELETION OF HUMAN ERYTHROCYTE ANKYRIN GENE ON CHROMOSOME-8 [J]. NATURE, 1990, 345 (6277) : 736 - 739

[10] HEREDITARY SPHEROCYTIC ANEMIA WITH DELETION OF THE SHORT ARM OF CHROMOSOME-8 [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1995, 58 (03): : 225 - 229