-
1
-
-
0024544273
-
Interstitial deletion of the long arm of chromosome 6(q22.2q23) in a boy with phenotypic features of Williams syndrome
-
Bzdúch V, Lukáčová 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
-
-
Bzdúch, V.1
Lukáčová, M.2
-
2
-
-
0024334717
-
Interstitial deletion of the long arm of chromosome 6
-
Chery M,de F Formiga L, Mujica P, André M, Stehelin D, Dozier C, Gilgenkrantz S. 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
De F Formiga, L.2
Mujica, P.3
André, M.4
Stehelin, D.5
Dozier, C.6
Gilgenkrantz, S.7
-
3
-
-
0019417862
-
A de novo interstitial deletion of band q21 on chromosome 6
-
Côté 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
-
-
Côté, G.B.1
Papadakou-Lagoyanni, S.2
Metaxotou, C.3
-
4
-
-
0026005051
-
Prune-belly anomaly and large interstitial deletion of the long arm of chromosome 6
-
Fryns JP, Vandenberghe K, Van den Berghe H. Prune-belly anomaly and large interstitial deletion of the long arm of chromosome 6. Ann Genet 1991: 34: 127.
-
(1991)
Ann Genet
, vol.34
, pp. 127
-
-
Fryns, J.P.1
Vandenberghe, K.2
Van Den Berghe, H.3
-
5
-
-
0023929741
-
Partial monosomy 6q(q15q21) by de novo interstitial deletion
-
Glover G, López I, Gabarrón 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
López, I.2
Gabarrón, J.3
Carmona, J.A.4
-
6
-
-
0026102051
-
Interstitial deletion of the long arm of chromosome 6 associated with absent pulmonary valve
-
Horigome H, Takano T, HiranoT, Kajima T, Ohtani S. Interstitial deletion of the long arm of chromosome 6 associated with absent pulmonary valve. Am J Med Genet 1991: 38: 608-611.
-
(1991)
Am J Med Genet
, vol.38
, pp. 608-611
-
-
Horigome, H.1
Takano, T.2
Hirano, T.3
Kajima, T.4
Ohtani, S.5
-
7
-
-
0023868809
-
A malformed girl with a de novo proximal 6q deletion
-
Lonardo F, Colantuoni M, Festa B, Gentile G, Guerritore G, Perone L, Santulli B, Ventruto V. 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
Gentile, G.4
Guerritore, G.5
Perone, L.6
Santulli, B.7
Ventruto, V.8
-
8
-
-
0025157110
-
Chromosome 6q deletions: A report of two additional cases and a review of the literature
-
McLeod DR, Fowlow SB, Robertson A, Samcoe D, Burgess I, Hoo JJ. 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
Samcoe, D.4
Burgess, I.5
Hoo, J.J.6
-
9
-
-
0018837255
-
Interstitial deletion 6q in a malformed boy
-
Paris
-
Nakagome Y, Tanaka T, Hashimoto T, Kuyama N, Maruyama M. Interstitial deletion 6q in a malformed boy. Ann Genet (Paris) 1980: 23: 49-51.
-
(1980)
Ann Genet
, vol.23
, pp. 49-51
-
-
Nakagome, Y.1
Tanaka, T.2
Hashimoto, T.3
Kuyama, N.4
Maruyama, M.5
-
10
-
-
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, Yokayama Y, Namba H, Hurakami M, Matsubara T, Kasai R, Fukushima Y, Seki T, Wakui K, Seino Y. 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
Yokayama, Y.3
Namba, H.4
Hurakami, M.5
Matsubara, T.6
Kasai, R.7
Fukushima, Y.8
Seki, T.9
Wakui, K.10
Seino, Y.11
-
12
-
-
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, Desnick RJ. 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
Desnick, R.J.4
-
13
-
-
0023862956
-
Interstitial deletion(6)(q11q15) in an infant with congenital abnormalities
-
Slater HR, Robb A, Forsyth LA, Hamilton DA, Clark MC, Galloway CAS. Interstitial deletion(6)(q11q15) in an infant with congenital abnormalities. J Med Genel 1988: 25: 210-211.
-
(1988)
J Med Genel
, vol.25
, pp. 210-211
-
-
Slater, H.R.1
Robb, A.2
Forsyth, L.A.3
Hamilton, D.A.4
Clark, M.C.5
Galloway, C.A.S.6
-
14
-
-
0028194918
-
Prader-Will-like phenotype in fragile X syndrome
-
Schrander-Stumpel C, Gerver W-J, Meyer H, Engelen J, Mulder H, Fryns J-P. Prader-Will-like phenotype in fragile X syndrome. Clin Genet 1994: 45: 175-180.
-
(1994)
Clin Genet
, vol.45
, pp. 175-180
-
-
Schrander-Stumpel, C.1
Gerver, W.-J.2
Meyer, H.3
Engelen, J.4
Mulder, H.5
Fryns, J.-P.6
-
15
-
-
0023683122
-
6q1 monosomy: A distinctive syndrome
-
Turleau C, Demay G, Cabanis M-O, Lenoir G, de Grouchy J. 6q1 monosomy: a distinctive syndrome. Clin Genet 1988: 34: 38-42.
-
(1988)
Clin Genet
, vol.34
, pp. 38-42
-
-
Turleau, C.1
Demay, G.2
Cabanis, M.-O.3
Lenoir, G.4
De Grouchy, J.5
-
16
-
-
0026521872
-
Monosomy 6q: Report on four new cases
-
Valtat C, Galliano D, Mettey R, Toutain A, Moraine C. Monosomy 6q: report on four new cases. Clin Genet 1992: 41: 159-166.
-
(1992)
Clin Genet
, vol.41
, pp. 159-166
-
-
Valtat, C.1
Galliano, D.2
Mettey, R.3
Toutain, A.4
Moraine, C.5
-
17
-
-
0027282296
-
Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype
-
de Vries BBA, Fryns JP, Butler MG, Canziani F, Wesby-van Swaay E, van Hemel JO, Oostra BA, Halley DJJ, Niermeijer MF. Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype. J Med Genet 1993: 30: 761-766.
-
(1993)
J Med Genet
, vol.30
, pp. 761-766
-
-
De Vries, B.B.A.1
Fryns, J.P.2
Butler, M.G.3
Canziani, F.4
Wesby-van Swaay, E.5
Van Hemel, J.O.6
Oostra, B.A.7
Halley, D.J.J.8
Niermeijer, M.F.9
-
18
-
-
0027946237
-
The Prader-Willi-like phenotype in fragile X patients: A designation facilitating clinical (and molecular) differential diagnosis
-
de Vries BBA, Niermeijer MF. The Prader-Willi-like phenotype in fragile X patients: a designation facilitating clinical (and molecular) differential diagnosis. J Med Genet 1994: 31: 820.
-
(1994)
J Med Genet
, vol.31
, pp. 820
-
-
De Vries, B.B.A.1
Niermeijer, M.F.2
-
21
-
-
0022536187
-
Deletion of proximal 6q: A clinical report and review of the literature
-
Yamamoto Y, Okamoto N, Shiraishi H, Yanagisawa M, Kamoshita S. 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
Yanagisawa, M.4
Kamoshita, S.5
-
22
-
-
0022001559
-
Deletions of the long arm of chromosome 6: Two new cases and review of the literature
-
Young RS, Fidone GS, Reider-Garcia PA, Hansen KL, Mc-Combs JL, Moore CM. 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
Hansen, K.L.4
Mc-Combs, J.L.5
Moore, C.M.6
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