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1
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0021073329
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Interstitial deletion of the long arm of chromosome 2: Del(2)(q31q33)
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Al-Awadi SA, Farag TI, Naguib K, Teebi A, Cuschieri A, Al-Othman S, Sundareshan T (1983): Interstitial deletion of the long arm of chromosome 2: del(2)(q31q33). J Med Genet 20: 464465
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(1983)
J Med Genet
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Al-Awadi, S.A.1
Farag, T.I.2
Naguib, K.3
Teebi, A.4
Cuschieri, A.5
Al-Othman, S.6
Sundareshan, T.7
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2
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33646788108
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De novo interstitial deletion of the long arm of chromosome 2 in a malformed newborn karyotype: 46,XY,del(2)(ql2ql4)
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Antich J, Carbonell X, Clusellas N (1981): De novo interstitial deletion of the long arm of chromosome 2 in a malformed newborn karyotype: 46,XY,del(2)(ql2ql4). Clin Genet 19: 489
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(1981)
Clin Genet
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, pp. 489
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Antich, J.1
Carbonell, X.2
Clusellas, N.3
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3
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0022467685
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Interstitial deletion of the long arm of chromosome 2 in a malformed infant with karyotype 46,XX,del(2)(q31q33)
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Benson K, Gordon M, Wassman ER, Chung T (1986): Interstitial deletion of the long arm of chromosome 2 in a malformed infant with karyotype 46,XX,del(2)(q31q33). Am J Med Genet 25: 405-411
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(1986)
Am J Med Genet
, vol.25
, pp. 405-411
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Benson, K.1
Gordon, M.2
Wassman, E.R.3
Chung, T.4
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4
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0021842966
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Interstitial deletion 2q24.3: Case report with high resolution banding
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Bernar J, Sparkes R, Allensworth S (1984): Interstitial deletion 2q24.3: case report with high resolution banding. J Med Genet 22: 226-228
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(1984)
J Med Genet
, vol.22
, pp. 226-228
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Bernar, J.1
Sparkes, R.2
Allensworth, S.3
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5
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0028963512
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Deletion of chromosome 2q24-q31 causes characteristic digital anomalies: Case report and review
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Boles RG, Pober BR, Gibson LH, Willis CR, McGrath J, Roberts DJ, Yang-Feng TL (1995): Deletion of chromosome 2q24-q31 causes characteristic digital anomalies: case report and review. Am J Med 55: 155-160
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(1995)
Am J Med
, vol.55
, pp. 155-160
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Boles, R.G.1
Pober, B.R.2
Gibson, L.H.3
Willis, C.R.4
McGrath, J.5
Roberts, D.J.6
Yang-Feng, T.L.7
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7
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0028073577
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Small terminal deletions of the long arm of chromosome 2: Two new cases
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Fisher AM, Ellis KH, Browne CE, Barber JCK, Barker M, Kennedy CR, Foley H, Patton MA ( 1994): Small terminal deletions of the long arm of chromosome 2: two new cases. Am J Med Genet 53: 366-369
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(1994)
Am J Med Genet
, vol.53
, pp. 366-369
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Fisher, A.M.1
Ellis, K.H.2
Browne, C.E.3
Jck, B.4
Barker, M.5
Kennedy, C.R.6
Foley, H.7
Ma, P.8
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8
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0020959116
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Interstitial deletion of the long arm of chromosome 2 (q31q33) in a girl with multiple anomalies and mental retardation
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Franceschini P, Silengo MC, Davi G, Biano R, Biagioli M (1983): Interstitial deletion of the long arm of chromosome 2 (q31q33) in a girl with multiple anomalies and mental retardation. Hum Genet 64: 98
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(1983)
Hum Genet
, vol.64
, pp. 98
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Franceschini, P.1
Silengo, M.C.2
Davi, G.3
Biano, R.4
Biagioli, M.5
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9
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0017738809
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Interstitial deletion of the long arm of chromosome 2 in a polymalformed newborn-karyotype: 46,XX,del(2)(q21;q24)
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Fryns JP, Van Bosstraeten B, Malbrain H, Van den Berghe H (1977): Interstitial deletion of the long arm of chromosome 2 in a polymalformed newborn-karyotype: 46,XX,del(2)(q21;q24). Hum Genet 39: 233-238
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(1977)
Hum Genet
, vol.39
, pp. 233-238
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Fryns, J.P.1
Van Bosstraeten, B.2
Malbrain, H.3
Van Den Berghe, H.4
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10
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0024575079
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Interstitial deletion of the long arm of chromosome 2 with normal levels of isocitrate dehydrogenase
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Glass IA, Swindlehurst CA, Aitken DA, McCrea W, Boyd E (1989): Interstitial deletion of the long arm of chromosome 2 with normal levels of isocitrate dehydrogenase. J Med Genet 26: 127-140
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(1989)
J Med Genet
, vol.26
, pp. 127-140
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Glass, I.A.1
Swindlehurst, C.A.2
Aitken, D.A.3
McCrea, W.4
Boyd, E.5
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11
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0021960309
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Interstitial deletion of chromosome 2
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Markovic S, Krstic M, Sulovic V, Radojkovic Z, Adzic S (1985): Interstitial deletion of chromosome 2. J Med Genet 22: 154-155
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(1985)
J Med Genet
, vol.22
, pp. 154-155
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Markovic, S.1
Krstic, M.2
Sulovic, V.3
Radojkovic, Z.4
Adzic, S.5
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12
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0018823281
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Partial deletion of chromosome 2 mimicking a phenotype of trisomy 18: Case report with autopsy
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McConnell TS, Kornfeld M, McClellan G, Aase J (1980): Partial deletion of chromosome 2 mimicking a phenotype of trisomy 18: case report with autopsy. Hum Pathol 11: 202-205
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(1980)
Hum Pathol
, vol.11
, pp. 202-205
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McConnell, T.S.1
Kornfeld, M.2
McClellan, G.3
Aase, J.4
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13
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0021713448
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Pure monosomy and trisomy 2q24.1→q3105 due to an inv ins(7;2)(q21.2;q3105q24.2) segregating in four generations
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Moller M, Garcîa-Cruz D, Rivera H, Sänchez-Corona J, Cantu JM (1984): Pure monosomy and trisomy 2q24.1→q3105 due to an inv ins(7;2)(q21.2;q3105q24.2) segregating in four generations. Hum Genet 68: 77-86
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(1984)
Hum Genet
, vol.68
, pp. 77-86
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Moller, M.1
Garcîa-Cruz, D.2
Rivera, H.3
Sänchez-Corona, J.4
Cantu, J.M.5
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15
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0020673351
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Identical multiple congenital anomalies/Mental retardation (MCA/MR) syndrome due to del(2)(q32) in two sisters with intrachromosomal insertional translocation in their father
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Pai GS, Rogers JF, Sommer A (1983): Identical multiple congenital anomalies/Mental retardation (MCA/MR) syndrome due to del(2)(q32) in two sisters with intrachromosomal insertional translocation in their father. Am J Med Genet 14: 189-195
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(1983)
Am J Med Genet
, vol.14
, pp. 189-195
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Pai, G.S.1
Rogers, J.F.2
Sommer, A.3
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16
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0024391670
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A review of phenotype-karyotype correlations in individuals with interstitial deletions of the long arm of chromosome 2
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Ramer JC, Ladda RL, Frankel CA, Beckford A (1989): A review of phenotype-karyotype correlations in individuals with interstitial deletions of the long arm of chromosome 2. Am J Med Genet 32: 359-363
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(1989)
Am J Med Genet
, vol.32
, pp. 359-363
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Ramer, J.C.1
Ladda, R.L.2
Frankel, C.A.3
Beckford, A.4
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17
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0019968564
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Partial monosomy of chromosome 2. Delineable syndrome of deletion 2 (q23-q31)
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Shabtai F, Klar D, Halbrecht I (1982): Partial monosomy of chromosome 2. Delineable syndrome of deletion 2 (q23-q31). Ann Genet 25: 156-158
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(1982)
Ann Genet
, vol.25
, pp. 156-158
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Shabtai, F.1
Klar, D.2
Halbrecht, I.3
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18
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0019833247
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Interstitial deletion of the long arm of chromosome 2. Case report and review of literature
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Taysi K, Dengler DR, Jones LA, Heersma JR (1981): Interstitial deletion of the long arm of chromosome 2. Case report and review of literature. Ann Genet 24: 245-247
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(1981)
Ann Genet
, vol.24
, pp. 245-247
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Taysi, K.1
Dengler, D.R.2
Jones, L.A.3
Heersma, J.R.4
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19
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0025727923
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Interstitial deletion del(2)(q24q3I) with a phenotype similar to del(2)(q31q33)
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Wamsler C, Muller B, Freyberger G, Schmid M (1991): Interstitial deletion del(2)(q24q3I) with a phenotype similar to del(2)(q31q33). Am J Med Genet 39: 204-206
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(1991)
Am J Med Genet
, vol.39
, pp. 204-206
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Wamsler, C.1
Muller, B.2
Freyberger, G.3
Schmid, M.4
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20
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0017184826
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Etude chromosomique et clinique d'une fillette porteuse d'une deletion (2)(q31q36)
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Warter S, Lausecker C, Pennerath A (1976): Etude chromosomique et clinique d'une fillette porteuse d'une deletion (2)(q31q36). Hum Genet 32: 225-227
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(1976)
Hum Genet
, vol.32
, pp. 225-227
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Warter, S.1
Lausecker, C.2
Pennerath, A.3
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21
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0020521543
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Deletion 2q: Two new cases with karyotypes 46,XY,del(2)(q31q33) and 46,XX,del(2)(q36)
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Young RS, Shapiro SD, Hansen K, Hine RK, Rainosek D, Guerra FA (1983): Deletion 2q: two new cases with karyotypes 46,XY,del(2)(q31q33) and 46,XX,del(2)(q36). J Med Genêt 20: 199-202
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(1983)
J Med Genêt
, vol.20
, pp. 199-202
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Young, R.S.1
Shapiro, S.D.2
Hansen, K.3
Hine, R.K.4
Rainosek, D.5
Guerra, F.A.6
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