Authors:
Tuck-Muller, CM
Goodman, BK
Li, SB
Martinez, JE
Chen, XN
Wertelecki, W
Korenberg, JR
Stetten, G
Citation: Cm. Tuck-muller et al., Partial trisomy 7p defined by analysis of a complex chromosome rearrangement using a BAC clone panel, GENET MED, 3(2), 2001, pp. 126-131
Authors:
Praphanphoj, V
Goodman, BK
Thomas, GH
Niel, KM
Toomes, C
Dixon, MJ
Geraghty, MT
Citation: V. Praphanphoj et al., Molecular cytogenetic evaluation in a patient with a translocation (3;21) associated with blepharophimosis, ptosis, epicanthus inversus syndrome (BPES), GENOMICS, 65(1), 2000, pp. 67-69
Authors:
Cargile, CB
McIntosh, I
Clough, MV
Rutberg, J
Yaghmai, R
Goodman, BK
Chen, XN
Korenberg, JR
Thomas, GH
Geraghty, MT
Citation: Cb. Cargile et al., Delayed membranous ossification of the cranium associated with familial translocation (2;3)(p15;q12), AM J MED G, 92(5), 2000, pp. 328-335
Authors:
Sacksteder, KA
Biery, BJ
Morrell, JC
Goodman, BK
Geisbrecht, BV
Cox, RP
Gould, SJ
Geraghty, MT
Citation: Ka. Sacksteder et al., Identification of the alpha-aminoadipic semialdehyde synthase gene, which is defective in familial hyperlysinemia, AM J HU GEN, 66(6), 2000, pp. 1736-1743
Authors:
Camacho, JA
Obie, C
Biery, B
Goodman, BK
Hu, CA
Almashanu, S
Steel, G
Casey, R
Lambert, M
Mitchell, GA
Valle, D
Citation: Ja. Camacho et al., Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome is caused bymutations in a gene encoding a mitochondrial ornithine transporter, NAT GENET, 22(2), 1999, pp. 151-158
Authors:
Goodman, BK
Stone, K
Coddett, JM
Cargile, CB
Gurewitsch, ED
Blakemore, KJ
Stetten, G
Citation: Bk. Goodman et al., Molecular cytogenetic analysis and clinical findings in a newborn with prenatally diagnosed rec(7)dup(7q)inv(7)(p22q31.3)pat, PRENAT DIAG, 19(12), 1999, pp. 1150-1156
Authors:
Sigurdardottir, S
Goodman, BK
Rutberg, J
Thomas, GH
Jabs, EW
Geraghty, MT
Citation: S. Sigurdardottir et al., Clinical, cytogenetic, and fluorescence in situ hybridization findings in two cases of ''complete ring" syndrome, AM J MED G, 87(5), 1999, pp. 384-390
Authors:
Goodman, BK
Shaffer, LG
Rutberg, J
Leppert, M
Harum, K
Gagos, S
Ray, JH
Bialer, MG
Zhou, XT
Pletcher, BA
Shapira, SK
Geraghty, MT
Citation: Bk. Goodman et al., Inherited duplication Xq27-qter at Xp22.3 in severely affected males: Molecular cytogenetic evaluation and clinical description in three unrelated families, AM J MED G, 80(4), 1998, pp. 377-384