-
1
-
-
0023182545
-
A child with partial monosomy 6q secondary to a maternal direct insertional event
-
Matkins SV, Meyer JE, Beny AC: A child with partial monosomy 6q secondary to a maternal direct insertional event. J Med Genet 1987; 24:227-229.
-
(1987)
J Med Genet
, vol.24
, pp. 227-229
-
-
Matkins, S.V.1
Meyer, J.E.2
Beny, A.C.3
-
2
-
-
0025157110
-
Chromosome 6q deletions: A report of two additional cases and a review of the literature
-
McLeod DR, Fowlow SB, Robertson A, et al: Chromosome 6q deletions: A report of two additional cases and a review of the literature. Am J Med Genet 1990;35:79-84.
-
(1990)
Am J Med Genet
, vol.35
, pp. 79-84
-
-
McLeod, D.R.1
Fowlow, S.B.2
Robertson, A.3
-
3
-
-
0025738388
-
Specification of small distal 6q deletions in two patients by gene dosage and in situ hybridization study of plasminogen and alpha-L-fucosidase 2
-
Narahara K, Tsuji K, Yokoyama Y, et al: Specification of small distal 6q deletions in two patients by gene dosage and in situ hybridization study of plasminogen and alpha-L-fucosidase 2. Am J Med Genet 1991;40:348-353.
-
(1991)
Am J Med Genet
, vol.40
, pp. 348-353
-
-
Narahara, K.1
Tsuji, K.2
Yokoyama, Y.3
-
4
-
-
0029874862
-
Interstitial deletion of chromosome 6q: Precise definition of the breakpoints by microdissection, DNA amplification, and reverse painting
-
Rubtsov N, Senger G, Kuzcera H, et al: Interstitial deletion of chromosome 6q: Precise definition of the breakpoints by microdissection, DNA amplification, and reverse painting. Hum Genet 1996;97:705-709.
-
(1996)
Hum Genet
, vol.97
, pp. 705-709
-
-
Rubtsov, N.1
Senger, G.2
Kuzcera, H.3
-
5
-
-
0026521872
-
Monosomy 6q: Report on four new cases
-
Valtat G, Galliano D, Mettey R, et al: Monosomy 6q: Report on four new cases. Clin Genet 1992;41:159-166.
-
(1992)
Clin Genet
, vol.41
, pp. 159-166
-
-
Valtat, G.1
Galliano, D.2
Mettey, R.3
-
6
-
-
0030906366
-
New insights into the phenotypes of 6q deletions
-
Hopkin RJ, Schorry E, Bofinger M, et al: New insights into the phenotypes of 6q deletions. Am J Genet 1997;70:377-386.
-
(1997)
Am J Genet
, vol.70
, pp. 377-386
-
-
Hopkin, R.J.1
Schorry, E.2
Bofinger, M.3
-
7
-
-
0026717065
-
Two patients with chromosome 6q terminal deletions with breakpoints at q24.3 and q25.3
-
Meng J, Fujita H, Nagahara N, et al: Two patients with chromosome 6q terminal deletions with breakpoints at q24.3 and q25.3. Am J Med Genet 1992;43(4):747-750.
-
(1992)
Am J Med Genet
, vol.43
, Issue.4
, pp. 747-750
-
-
Meng, J.1
Fujita, H.2
Nagahara, N.3
-
9
-
-
0041821976
-
Complex MCA/MR syndrome associated with interstitial deletion of the long arm of chromosome 6, del(6)(q25.1-q27)
-
Vermeesch JR, Fryns JP: Complex MCA/MR syndrome associated with interstitial deletion of the long arm of chromosome 6, del(6)(q25.1-q27). Am J Med Genet 2003;120A:299-300.
-
(2003)
Am J Med Genet
, vol.120 A
, pp. 299-300
-
-
Vermeesch, J.R.1
Fryns, J.P.2
-
10
-
-
0031786268
-
Agenesis of the corpus callosum with Probst bundles owing to haploinsufficiency for a gene in an 8 cM region of 6q25
-
Pirola B, Bortotto L, Giglio S, et al: Agenesis of the corpus callosum with Probst bundles owing to haploinsufficiency for a gene in an 8 cM region of 6q25. J Med Genet 1998;35:1031-1033.
-
(1998)
J Med Genet
, vol.35
, pp. 1031-1033
-
-
Pirola, B.1
Bortotto, L.2
Giglio, S.3
-
11
-
-
0016723791
-
Long arm deletion of chromosome no.6 in a mentally retarded boy with multiple physical malformations
-
Milosevic J, Kalicanin P: Long arm deletion of chromosome no.6 in a mentally retarded boy with multiple physical malformations. J Ment Defic Res 1975;19:139-144.
-
(1975)
J Ment Defic Res
, vol.19
, pp. 139-144
-
-
Milosevic, J.1
Kalicanin, P.2
-
12
-
-
0033527729
-
Subtle overlapping deletions in the terminal region of chromosome 6q24.2-q26: Three cases studied using FISH
-
Sukumar S, Wang S, Hoang K, et al: Subtle overlapping deletions in the terminal region of chromosome 6q24.2-q26: Three cases studied using FISH. Am J Med Genet 1999;87:17-22.
-
(1999)
Am J Med Genet
, vol.87
, pp. 17-22
-
-
Sukumar, S.1
Wang, S.2
Hoang, K.3
-
13
-
-
0017756843
-
Congenital anomalies including the VATER association in a patient with del(6)q deletion
-
McNeal RM, Skoglund RR, Francke U: Congenital anomalies including the VATER association in a patient with del(6)q deletion. J Pediatr 1977;91:957-960.
-
(1977)
J Pediatr
, vol.91
, pp. 957-960
-
-
McNeal, R.M.1
Skoglund, R.R.2
Francke, U.3
-
14
-
-
0018837255
-
Interstitial deletion 6q in a malformed boy
-
Nakamore Y, Tanaka T, Hashimoto T, et al: Interstitial deletion 6q in a malformed boy. Ann Genet 1980;23:49-51.
-
(1980)
Ann Genet
, vol.23
, pp. 49-51
-
-
Nakamore, Y.1
Tanaka, T.2
Hashimoto, T.3
-
15
-
-
0019417862
-
A de novo interstitial deletion of band q21 on chromosome 6
-
Cote GB, Papadakou-Lagoyanni S, Metaxotou C: A de novo interstitial deletion of band q21 on chromosome 6. Ann Genet 1981;24:170-171.
-
(1981)
Ann Genet
, vol.24
, pp. 170-171
-
-
Cote, G.B.1
Papadakou-Lagoyanni, S.2
Metaxotou, C.3
-
16
-
-
0021673508
-
Interstitial deletion of the long arm of chromosome 6[del(6) (q16q22)]: Case report and review of the literature
-
Schwartz MF, Kaffe S, Wallace S, et al: Interstitial deletion of the long arm of chromosome 6[del(6) (q16q22)]: Case report and review of the literature. Clin Genet 1984;26:574-578.
-
(1984)
Clin Genet
, vol.26
, pp. 574-578
-
-
Schwartz, M.F.1
Kaffe, S.2
Wallace, S.3
-
17
-
-
0022001559
-
Deletions of the long arm of chromosome 6: Two new cases and review of the literature
-
Young RS, Fidone GS, Reider-Garcia PA, et al: Deletions of the long arm of chromosome 6: Two new cases and review of the literature. Am J Med Genet 1985;20:21-29.
-
(1985)
Am J Med Genet
, vol.20
, pp. 21-29
-
-
Young, R.S.1
Fidone, G.S.2
Reider-Garcia, P.A.3
-
18
-
-
0022536187
-
Deletion of proximal 6q: A clinical report and review of the literature
-
Yamamoto Y, Okamoto N, Shiraishi H, et al: Deletion of proximal 6q: a clinical report and review of the literature. Am J Med Genet 1986;25: 467-471.
-
(1986)
Am J Med Genet
, vol.25
, pp. 467-471
-
-
Yamamoto, Y.1
Okamoto, N.2
Shiraishi, H.3
-
19
-
-
0023862956
-
Interstitial deletion (6)(q11-q15) in an infant with congenital abnormalities
-
Slater HR, Robb A, Forsyth LA, et al: Interstitial deletion (6)(q11-q15) in an infant with congenital abnormalities. J Med Genet 1988;25:210-211.
-
(1988)
J Med Genet
, vol.25
, pp. 210-211
-
-
Slater, H.R.1
Robb, A.2
Forsyth, L.A.3
-
20
-
-
0023929741
-
Partial monosomy 6q(q15q21) by de novo interstitial deletion
-
Glover G, Lopez I, Gabarron J, Carmona JA: Partial monosomy 6q(q15q21) by de novo interstitial deletion. Clin Genet 1988;33:308-310.
-
(1988)
Clin Genet
, vol.33
, pp. 308-310
-
-
Glover, G.1
Lopez, I.2
Gabarron, J.3
Carmona, J.A.4
-
21
-
-
0023868809
-
A malformed girl with a de novo proximal 6q deletion
-
Lonardo F, Colantuoni M, Festa B, et al: A malformed girl with a de novo proximal 6q deletion. Ann Genet 1988;31:57-59.
-
(1988)
Ann Genet
, vol.31
, pp. 57-59
-
-
Lonardo, F.1
Colantuoni, M.2
Festa, B.3
-
24
-
-
0024334717
-
Interstitial deletion of the long arm of chromosome 6
-
Chery M, Formiga LF, Mujica P, et al: Interstitial deletion of the long arm of chromosome 6. Ann Genet 1989;32:82-86.
-
(1989)
Ann Genet
, vol.32
, pp. 82-86
-
-
Chery, M.1
Formiga, L.F.2
Mujica, P.3
-
25
-
-
0024544273
-
Interstitial deletion of the long arm of chromosome 6 (q22.2q23) in a boy with phenotypic features of Williams syndrome
-
Bzduch V, Lukacova M: Interstitial deletion of the long arm of chromosome 6 (q22.2q23) in a boy with phenotypic features of Williams syndrome. Clin Genet 1989;35:230-231.
-
(1989)
Clin Genet
, vol.35
, pp. 230-231
-
-
Bzduch, V.1
Lukacova, M.2
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