-
1
-
-
0034706390
-
Phenotype of a patient with pure partial trisomy 2p(p23 → pter)
-
AL-SAFFAR M., LEMYRE E., KOENEKOOP R., DUNCAN A.M., DER KALOUSTIAN V.M.: Phenotype of a patient with pure partial trisomy 2p(p23 → pter). Am. J. Med. Genet., 2000, 94, 428-432.
-
(2000)
Am. J. Med. Genet.
, vol.94
, pp. 428-432
-
-
Al-Saffar, M.1
Lemyre, E.2
Koenekoop, R.3
Duncan, A.M.4
Der Kaloustian, V.M.5
-
2
-
-
0017855558
-
Partial 2p trisomy (p21 leads to pter) in two siblings of a family with a 2p-: 15q+ translocation
-
ARMENDARES S., SALAMANCA-GOMEZ F.: Partial 2p trisomy (p21 leads to pter) in two siblings of a family with a 2p-: 15q+ translocation. Clin. Genet., 1978, 13, 17-24.
-
(1978)
Clin. Genet.
, vol.13
, pp. 17-24
-
-
Armendares, S.1
Salamanca-Gomez, F.2
-
3
-
-
0028801633
-
Prenatally detected fetal myelomeningocele: Is karyotype analysis warranted?
-
BABCOOK C. J., GOLDSTEIN R. B., FILLY R.A.: Prenatally detected fetal myelomeningocele: is karyotype analysis warranted? Radiology, 1995, 194, 491-494.
-
(1995)
Radiology
, vol.194
, pp. 491-494
-
-
Babcook, C.J.1
Goldstein, R.B.2
Filly, R.A.3
-
4
-
-
0014585053
-
Familiäre 2/C-Translokation: 46, XY, t(2p-;Cp+) und 46,XX,Cp+
-
BENDER K., REINWEIN H., GORMAN L.Z., WOLF U.: Familiäre 2/C-Translokation: 46, XY, t(2p-;Cp+) und 46,XX,Cp+. Humangenetik, 1969, 8, 94-104.
-
(1969)
Humangenetik
, vol.8
, pp. 94-104
-
-
Bender, K.1
Reinwein, H.2
Gorman, L.Z.3
Wolf, U.4
-
6
-
-
0017652560
-
The chromosome 2 distal short arm trisomy syndrome
-
CASSIDY S.B., HELLER R.M., CHAZENE M., ENGEL E.: The chromosome 2 distal short arm trisomy syndrome. J. Pedlatr., 1977, 91, 934-938.
-
(1977)
J. Pedlatr.
, vol.91
, pp. 934-938
-
-
Cassidy, S.B.1
Heller, R.M.2
Chazene, M.3
Engel, E.4
-
7
-
-
0024905706
-
Aneuploidy with neural tube defects: Another reason for complete evaluation in patients with suspected ultrasound anomalies or elevated maternal serum alpha-fetoprotein
-
DRUGAN A., JOHNSON M.P., DVORIN E., MOODY J., KRIVCHENIA E.L., SCHWARTZ D., EVANS M.L: Aneuploidy with neural tube defects: another reason for complete evaluation in patients with suspected ultrasound anomalies or elevated maternal serum alpha-fetoprotein. Fetal Ther., 1989, 4, 88-92.
-
(1989)
Fetal Ther.
, vol.4
, pp. 88-92
-
-
Drugan, A.1
Johnson, M.P.2
Dvorin, E.3
Moody, J.4
Krivchenia, E.L.5
Schwartz, D.6
Evans, M.L.7
-
8
-
-
0038553734
-
Two cases of de novo partial trisomy 2pter diagnosed by CGH and FISH: Unbalanced translocation t(2;12)(p24;q24.3) and dup(2)(p23pter)
-
ENGELS H., SLEEGERS E., SPITZ R., ALBRECHT B., PASSARGE E., PROPPING P., SCHWANITZ G.: Two cases of de novo partial trisomy 2pter diagnosed by CGH and FISH: unbalanced translocation t(2;12)(p24;q24.3) and dup(2)(p23pter). Med. Genetik, 1999, 11, 4-14.
-
(1999)
Med. Genetik
, vol.11
, pp. 4-14
-
-
Engels, H.1
Sleegers, E.2
Spitz, R.3
Albrecht, B.4
Passarge, E.5
Propping, P.6
Schwanitz, G.7
-
9
-
-
0020578734
-
Variable phenotype associated with duplication of different regions of 2p
-
FINEMAN R.M., BUYSE M., MORGAN M.: Variable phenotype associated with duplication of different regions of 2p. Am. J. Med. Genet., 1983, 15, 451-456.
-
(1983)
Am. J. Med. Genet.
, vol.15
, pp. 451-456
-
-
Fineman, R.M.1
Buyse, M.2
Morgan, M.3
-
10
-
-
0017102041
-
The 2p partial trisomy syndrome. Duplication of region 2p23 leads to 2pter in two members of a t(2;7) translocation kindred
-
FRANCKE U., JONES K.L.: The 2p partial trisomy syndrome. Duplication of region 2p23 leads to 2pter in two members of a t(2;7) translocation kindred. Am. J. Dis. Child., 1976, 130, 1244-1249.
-
(1976)
Am. J. Dis. Child.
, vol.130
, pp. 1244-1249
-
-
Francke, U.1
Jones, K.L.2
-
11
-
-
0022883822
-
The fetal phenotype in 2p trisomy
-
FRYNS J.P., KLECZKOWSKA A., MOERMAN F., VAN DEN BERGHE K, VAN DEN BERGHE H.: The fetal phenotype in 2p trisomy. Ann. Génét., 1986, 29, 269-271.
-
(1986)
Ann. Génét.
, vol.29
, pp. 269-271
-
-
Fryns, J.P.1
Kleczkowska, A.2
Moerman, F.3
Van Den Berghe, K.4
Van Den Berghe, H.5
-
12
-
-
0033527618
-
Trisomy 2p syndrome: A fetus with anencephaly and postaxial polydactyly
-
HAHM G.K., BARTH R.F., SCHAUER G.M., REISS R., OPITZ J.M.: Trisomy 2p syndrome: A fetus with anencephaly and postaxial polydactyly. Am. J. Med. Genet., 1999, 87, 45-48.
-
(1999)
Am. J. Med. Genet.
, vol.87
, pp. 45-48
-
-
Hahm, G.K.1
Barth, R.F.2
Schauer, G.M.3
Reiss, R.4
Opitz, J.M.5
-
13
-
-
0029073378
-
Prenatal ultrasound detection of isolated neural tube defects: Is cytogenetic evaluation warranted?
-
HARMON J.P., HIETT A.K, PALMER C.G., GOLICHOWSKI A.M.: Prenatal ultrasound detection of isolated neural tube defects: is cytogenetic evaluation warranted? Obstet. Gynecol., 1995, 86, 595-599.
-
(1995)
Obstet. Gynecol.
, vol.86
, pp. 595-599
-
-
Harmon, J.P.1
Hiett, A.K.2
Palmer, C.G.3
Golichowski, A.M.4
-
14
-
-
0025978732
-
Anterior segment mesenchymal dysgenesis associated with partial duplication of the short arm of chromosome 2
-
HEATHCOTE J.G., SHOLDICE J., WALTON J.C., WILLIS N.R., SERGOVICH F.R.: Anterior segment mesenchymal dysgenesis associated with partial duplication of the short arm of chromosome 2. Can. J. Ophtalmol., 1991, 26, 35-43.
-
(1991)
Can. J. Ophtalmol.
, vol.26
, pp. 35-43
-
-
Heathcote, J.G.1
Sholdice, J.2
Walton, J.C.3
Willis, N.R.4
Sergovich, F.R.5
-
15
-
-
0030047177
-
Aneuploidy among prenatally detected neural tube defect
-
HUME R.F. Jr, DRUGAN A., REICHLER A., LAMPINEN J., MARTIN L.S., JOHNSON M.P., EVANS M.L: Aneuploidy among prenatally detected neural tube defect. Am. J. Med. Genet., 1996, 61, 171-173.
-
(1996)
Am. J. Med. Genet.
, vol.61
, pp. 171-173
-
-
Hume R.F., Jr.1
Drugan, A.2
Reichler, A.3
Lampinen, J.4
Martin, L.S.5
Johnson, M.P.6
Evans, M.L.7
-
16
-
-
0031021071
-
Tetramelic Mirror-Image polydactyly and a de novo balanced translocation between 2p23.3 and 14q13
-
KIM K.C., WAKUI K., YAMAGISHI A., OHNO T., SATO M., IMAIZUMI S., AIHARA T., FUKUSHIMA Y., OHASHI H.: Tetramelic Mirror-Image polydactyly and a de novo balanced translocation between 2p23.3 and 14q13. Am. J. Med. Genet., 1997, 68, 70-73.
-
(1997)
Am. J. Med. Genet.
, vol.68
, pp. 70-73
-
-
Kim, K.C.1
Wakui, K.2
Yamagishi, A.3
Ohno, T.4
Sato, M.5
Imaizumi, S.6
Aihara, T.7
Fukushima, Y.8
Ohashi, H.9
-
17
-
-
0019190166
-
A case of partial trisomy 2p (region 2p21 to 2pter) derived from a maternal t(2;15) (p21;26)
-
KISHI K., MATSUTANI Y., IWATSUBO T., NISHIMURA K., TONOMURA A.: A case of partial trisomy 2p (region 2p21 to 2pter) derived from a maternal t(2;15) (p21;26). Jinrui Idengaku Zasshi, 1980, 25, 47-53.
-
(1980)
Jinrui Idengaku Zasshi
, vol.25
, pp. 47-53
-
-
Kishi, K.1
Matsutani, Y.2
Iwatsubo, T.3
Nishimura, K.4
Tonomura, A.5
-
18
-
-
0020059282
-
Familial reciprocal translocation, t(2;10)(p24;q26), resulting in duplication 2p and deletion 10q
-
LARSON L.M., WASDAHL W.A., SAUMUR J.H., COLEMAN M.L., HALL J.G., DOLAN C.R., SCHUTTA C.J.: Familial reciprocal translocation, t(2;10)(p24;q26), resulting in duplication 2p and deletion 10q. Clin. Genet., 1982, 21, 187-195,
-
(1982)
Clin. Genet.
, vol.21
, pp. 187-195
-
-
Larson, L.M.1
Wasdahl, W.A.2
Saumur, J.H.3
Coleman, M.L.4
Hall, J.G.5
Dolan, C.R.6
Schutta, C.J.7
-
19
-
-
0032213969
-
Neuronal patterning by BMPs: A requirement for GDF7 in the generation of a discrete class of commissural interneurons in the mouse spinal cord
-
LEE K.J., MENDELSOHN M., JESSELL T.M.: Neuronal patterning by BMPs: a requirement for GDF7 in the generation of a discrete class of commissural interneurons in the mouse spinal cord, Genes Dev., 1998, 12, 3394-3407.
-
(1998)
Genes Dev.
, vol.12
, pp. 3394-3407
-
-
Lee, K.J.1
Mendelsohn, M.2
Jessell, T.M.3
-
20
-
-
0028925114
-
Trisomy 2p: Analysis of unusual phenotypic findings
-
LURIE I.W., ILYINA H.G., GUREVICH D.B., RUMYANTSEVA N.V., NAUMCHIK I.V., CASTELLAN C., HOELLER A., SCHINZEL A.: Trisomy 2p: Analysis of unusual phenotypic findings. Am. J. Med. Genet. 1995, 55, 229-236.
-
(1995)
Am. J. Med. Genet.
, vol.55
, pp. 229-236
-
-
Lurie, I.W.1
Ilyina, H.G.2
Gurevich, D.B.3
Rumyantseva, N.V.4
Naumchik, I.V.5
Castellan, C.6
Hoeller, A.7
Schinzel, A.8
-
21
-
-
0016743831
-
Gene dosage: Evidence for assignment of erythrocyte acid phosphatase locus to chromosome 2
-
MAGENIS R.E., KOLER R.D., LOVRIEN E., BIGLEY R.H., DUVAL M.C., OVERTON K.M.: Gene dosage: evidence for assignment of erythrocyte acid phosphatase locus to chromosome 2. Proc. Natl. Acad. Sci. USA, 1975, 72, 4526-4530.
-
(1975)
Proc. Natl. Acad. Sci. USA
, vol.72
, pp. 4526-4530
-
-
Magenis, R.E.1
Koler, R.D.2
Lovrien, E.3
Bigley, R.H.4
Duval, M.C.5
Overton, K.M.6
-
22
-
-
0038214907
-
Unbalanced autosomal chromosome translocation carried by mosaic mother of affected offspring
-
MARION R.W., ROJAS B.M., ROMANOWITZ H., LASLEY L.K., BORRAS L., MATE-KOLE J., POWELL S., SADEK K, CAINE E.: Unbalanced autosomal chromosome translocation carried by mosaic mother of affected offspring. Am. J. Hum. Genet., 1998, 63, 4s: A144.
-
(1998)
Am. J. Hum. Genet.
, vol.63
, Issue.4 S
-
-
Marion, R.W.1
Rojas, B.M.2
Romanowitz, H.3
Lasley, L.K.4
Borras, L.5
Mate-Kole, J.6
Powell, S.7
Sadek, K.8
Caine, E.9
-
23
-
-
0018163448
-
Trisomie partielle 2p par translocation familiale 2/6
-
MAYER U., SCHWANITZ G., GROSSE K.P., ETZOLD R.: Trisomie partielle 2p par translocation familiale 2/6. Ann. Génét., 1978, 21, 172-176.
-
(1978)
Ann. Génét.
, vol.21
, pp. 172-176
-
-
Mayer, U.1
Schwanitz, G.2
Grosse, K.P.3
Etzold, R.4
-
24
-
-
0030984039
-
Interstitial duplication of the short arm of chromosome 2: Report of a new case and review
-
MEGARBANE A., SOURATY N., PRIEUR M., THEOPHILE D., CHEDID P., AUGE J., VEKEMANS M.: Interstitial duplication of the short arm of chromosome 2: report of a new case and review. J. Med. Genet., 1997, 34, 783-786.
-
(1997)
J. Med. Genet.
, vol.34
, pp. 783-786
-
-
Megarbane, A.1
Souraty, N.2
Prieur, M.3
Theophile, D.4
Chedid, P.5
Auge, J.6
Vekemans, M.7
-
25
-
-
0038553732
-
A case of partial 2p trisomy with thyroxine binding globulin deficiency
-
MITSUDO K., TANAKA M., HAYASHI K., UKITA M., KAJITANI T., KITANO H.: A case of partial 2p trisomy with thyroxine binding globulin deficiency. Annal. Paediatr. Japon., 1982, 28, 125-134.
-
(1982)
Annal. Paediatr. Japon.
, vol.28
, pp. 125-134
-
-
Mitsudo, K.1
Tanaka, M.2
Hayashi, K.3
Ukita, M.4
Kajitani, T.5
Kitano, H.6
-
26
-
-
0019361158
-
De novo partial 2p duplication with postmortem description
-
MONTELEONE P.L., BLAIR J.D., GRAVISS E.R., CHEN S.C., SALVADOR A., GRZEGOCKI J.A., MONTELEONE J.A.: De novo partial 2p duplication with postmortem description. Am. J. Med. Genet., 1981, 10, 55-64.
-
(1981)
Am. J. Med. Genet.
, vol.10
, pp. 55-64
-
-
Monteleone, P.L.1
Blair, J.D.2
Graviss, E.R.3
Chen, S.C.4
Salvador, A.5
Grzegocki, J.A.6
Monteleone, J.A.7
-
27
-
-
0019154755
-
A case of partial 2p trisomy with neuroblastoma
-
NAGANO H., KANO Y., KOBUCHI S., KAJITANI T.: A case of partial 2p trisomy with neuroblastoma. Jinrui Idengaku Zasshi, 1980, 25: 39-45.
-
(1980)
Jinrui Idengaku Zasshi
, vol.25
, pp. 39-45
-
-
Nagano, H.1
Kano, Y.2
Kobuchi, S.3
Kajitani, T.4
-
28
-
-
0018366940
-
Partial 2p trisomy in a 46,XY,der(5),t(2;5)(p23;p15)pat infant; autopsy findings
-
NEU R.L., DENNIS N.R., FISHER J.E.: Partial 2p trisomy in a 46,XY,der(5),t(2;5)(p23;p15)pat infant; autopsy findings. Ann. Génét., 1979, 22, 33-34.
-
(1979)
Ann. Génét.
, vol.22
, pp. 33-34
-
-
Neu, R.L.1
Dennis, N.R.2
Fisher, J.E.3
-
29
-
-
0038553735
-
Localization of human F12, F13A and ACP1
-
NIEBUHR E., EIBERG H., SCHOUSBOE L. Localization of human F12, F13A and ACP1. Cytogenet. Cell. Genet., 1985, 40, 714.
-
(1985)
Cytogenet. Cell. Genet.
, vol.40
, pp. 714
-
-
Niebuhr, E.1
Eiberg, H.2
Schousboe, L.3
-
30
-
-
0030771556
-
Germline duplication of chromosome 2p and neuroblastoma
-
PATEL J.S., PEARSON J., WILLATT, ANDREWS T., BEACH R., GREEN A.: Germline duplication of chromosome 2p and neuroblastoma. J. Med. Genet., 1997, 34, 949-951.
-
(1997)
J. Med. Genet.
, vol.34
, pp. 949-951
-
-
Patel, J.S.1
Pearson, J.2
Willatt3
Andrews, T.4
Beach, R.5
Green, A.6
-
31
-
-
0023613716
-
Partial trisomy 2p
-
PUESCHEL S.M., SCOLA P.S., MENDOZA T.: Partial trisomy 2p. J. Ment. Defic. Res., 1987, 31, 293-298.
-
(1987)
J. Ment. Defic. Res.
, vol.31
, pp. 293-298
-
-
Pueschel, S.M.1
Scola, P.S.2
Mendoza, T.3
-
32
-
-
0035371157
-
Unique case of trisomy 2p24.3-pter with no associated monosomy
-
ROGGENBUCK J.A., FINK J.M., MENDELSOHN N.J.: Unique case of trisomy 2p24.3-pter with no associated monosomy. Am. J. Med. Genet., 2001, 101, 50-54.
-
(2001)
Am. J. Med. Genet.
, vol.101
, pp. 50-54
-
-
Roggenbuck, J.A.1
Fink, J.M.2
Mendelsohn, N.J.3
-
33
-
-
0020061747
-
Partial duplication for the short arm of chromosome 2.: The 2p23 to pter syndrome
-
ROSENFELD W., VERMA R.S., JHAVERI R., DOSIK H., EVANS H.: Partial duplication for the short arm of chromosome 2.: the 2p23 to pter syndrome. Ann. Génét., 1982, 25: 28-31.
-
(1982)
Ann. Génét.
, vol.25
, pp. 28-31
-
-
Rosenfeld, W.1
Verma, R.S.2
Jhaveri, R.3
Dosik, H.4
Evans, H.5
-
34
-
-
0026670273
-
Multiple congenital anomalies due to partial 2p13-2pter duplication resulting from an unbalanced X;2 translocation
-
SARDA P., LEFORT G., DEVAUX P., HUMEAU C., RIEU D.: Multiple congenital anomalies due to partial 2p13-2pter duplication resulting from an unbalanced X;2 translocation. Ann. Génét., 1992, 35, 117-120.
-
(1992)
Ann. Génét.
, vol.35
, pp. 117-120
-
-
Sarda, P.1
Lefort, G.2
Devaux, P.3
Humeau, C.4
Rieu, D.5
-
35
-
-
0019162396
-
Agenesis of the lung associated with a chromosomal abnormality (46, XX, 2p+)
-
SAY B., CARPENTER N.J., GIACOIA G., JEGATHESAN S.: Agenesis of the lung associated with a chromosomal abnormality (46, XX, 2p+). J. Med. Genet., 1980, 17, 477-478.
-
(1980)
J. Med. Genet.
, vol.17
, pp. 477-478
-
-
Say, B.1
Carpenter, N.J.2
Giacoia, G.3
Jegathesan, S.4
-
37
-
-
0020565656
-
Lungenagenesis bei partieller Trisomie 2p und 21q
-
SCHOBER P.H., MULLER W.D., BEHMEL A., BEHMELA., FRITSCH G., BEITZKE A.: Lungenagenesis bei partieller Trisomie 2p und 21q. Klin. Padiatr., 1983, 195, 291-293.
-
(1983)
Klin. Padiatr.
, vol.195
, pp. 291-293
-
-
Schober, P.H.1
Muller, W.D.2
Behmel, A.3
Behmel, A.4
Fritsch, G.5
Beitzke, A.6
-
38
-
-
0018124292
-
Partial trisomy for the short arm of chromosome 2 due to familial balanced translocation
-
SEKHON G.S., TAYSI K., RATH R.: Partial trisomy for the short arm of chromosome 2 due to familial balanced translocation. Hum. Genet., 1978, 44, 99-103.
-
(1978)
Hum. Genet.
, vol.44
, pp. 99-103
-
-
Sekhon, G.S.1
Taysi, K.2
Rath, R.3
-
39
-
-
0023428540
-
The value of chromosome analysis in cases of neural tube defects: A case of anencephaly associated with fetal dup(2)(p24-pter)
-
SINGER N., GERSER S., WARBURTON D.: The value of chromosome analysis in cases of neural tube defects: a case of anencephaly associated with fetal dup(2)(p24-pter). Prenat. Diagn., 1987, 7, 567-571.
-
(1987)
Prenat. Diagn.
, vol.7
, pp. 567-571
-
-
Singer, N.1
Gerser, S.2
Warburton, D.3
-
40
-
-
0016261203
-
VORS: Translocation t(2;14) équilibrée chez une mère et trisomie partielle d'une partie du bras court d'un chromosome N° 2 chez deux de ses enfants
-
STOLL C., MESSER J., VORS: Translocation t(2;14) équilibrée chez une mère et trisomie partielle d'une partie du bras court d'un chromosome N° 2 chez deux de ses enfants. Ann. Génét., 1974, 17, 193-196.
-
(1974)
Ann. Génét.
, vol.17
, pp. 193-196
-
-
Stoll, C.1
Messer, J.2
-
41
-
-
0015616480
-
Presumptive direct insertion within chromosome 2 in man
-
THERKELSEN A.J., HULTEN M., JONASSON J., LINDSTEN J., CHRISTENSEN N.C., IVERSEN T.: Presumptive direct insertion within chromosome 2 in man. Ann. Hum. Genet., 1973, 36, 367-373.
-
(1973)
Ann. Hum. Genet.
, vol.36
, pp. 367-373
-
-
Therkelsen, A.J.1
Hulten, M.2
Jonasson, J.3
Lindsten, J.4
Christensen, N.C.5
Iversen, T.6
-
42
-
-
0027493364
-
Evidence for multi-site closure of the neural tube in humans
-
VAN ALLEN M.I., KALOUSEK D.K., CHERNOFF G.F., JURILOFF D., HARRIS M., MCGILLIVRAY B.C., YONG S.L., LANGLOIS S., MACLEOD P.M., CHITAYAT D., FRIEDMAN J.M., WILSON R.D., MCFADDEN D., PANTZAR J., RITCHIE S., HALL J.G.: Evidence for multi-site closure of the neural tube in humans. Am. J. Med. Genet., 1993, 47, 723-743.
-
(1993)
Am. J. Med. Genet.
, vol.47
, pp. 723-743
-
-
Van Allen, M.I.1
Kalousek, D.K.2
Chernoff, G.F.3
Juriloff, D.4
Harris, M.5
Mcgillivray, B.C.6
Yong, S.L.7
Langlois, S.8
Macleod, P.M.9
Chitayat, D.10
Friedman, J.M.11
Wilson, R.D.12
Mcfadden, D.13
Pantzar, J.14
Ritchie, S.15
Hall, J.G.16
-
43
-
-
0024083317
-
Cariotipo 46,XX,trcp(1;10), trcp(2;8) di origine materna e trisomia 2p
-
VIANELLO M.G., FASCE L., BESIO B., LUPI M., SCRIBANIS R., SBURLATTI C., BUONCOMPAGNI A.: Cariotipo 46,XX,trcp(1;10), trcp(2;8) di origine materna e trisomia 2p. Minerva Pediatr., 1988, 40, 561-569.
-
(1988)
Minerva Pediatr.
, vol.40
, pp. 561-569
-
-
Vianello, M.G.1
Fasce, L.2
Besio, B.3
Lupi, M.4
Scribanis, R.5
Sburlatti, C.6
Buoncompagni, A.7
-
44
-
-
0038553730
-
Faut-il caryotyper les parents d'enfants atteints d'anomalies de fermeture du tube neural
-
WALBAUM R., PEYRAT M.F., VAN DE VELDE M.F., GUEVIN DU MASGENET B., BETHOUART M., FARRIAUX J.P. Faut-il caryotyper les parents d'enfants atteints d'anomalies de fermeture du tube neural. J. Genet. Hum., 1984, 32, 307.
-
(1984)
J. Genet. Hum.
, vol.32
, pp. 307
-
-
Walbaum, R.1
Peyrat, M.F.2
Van De Velde, M.F.3
Guevin Du Masgenet, B.4
Bethouart, M.5
Farriaux, J.P.6
-
46
-
-
0030978737
-
A report of recurrent anencephaly with trisomy 2p23-2pter: Additional evidence for the involvement of 2p24 in neural tube development and evaluation of the role for cytogenetic analysis
-
WINSOR S.H., McGRATH M.J., KHALIFA M., DUNCAN A.M.: A report of recurrent anencephaly with trisomy 2p23-2pter: additional evidence for the involvement of 2p24 in neural tube development and evaluation of the role for cytogenetic analysis. Prenat. Diagn., 1997, 17, 665-669.
-
(1997)
Prenat. Diagn.
, vol.17
, pp. 665-669
-
-
Winsor, S.H.1
McGrath, M.J.2
Khalifa, M.3
Duncan, A.M.4
-
47
-
-
0026802070
-
Autosomal dominant congenital cataract and microphtalmia associated with a familial t(2,16) translocation
-
YOKOYAMA Y., NARAHARA K., TSUJI K., NINOMIYA S., SEINO Y.: Autosomal dominant congenital cataract and microphtalmia associated with a familial t(2,16) translocation. Hum. Genet., 1992, 90, 177-178.
-
(1992)
Hum. Genet.
, vol.90
, pp. 177-178
-
-
Yokoyama, Y.1
Narahara, K.2
Tsuji, K.3
Ninomiya, S.4
Seino, Y.5
-
48
-
-
0018599991
-
Direct duplication 2p14 → 2p23
-
YUNIS E., GONZALEZ J., ZUNIGA R., TORRES DE CABALLERO O.M., MONDRAGON A.: Direct duplication 2p14 → 2p23. Hum. Genet., 1979, 48, 241-244.
-
(1979)
Hum. Genet.
, vol.48
, pp. 241-244
-
-
Yunis, E.1
Gonzalez, J.2
Zuniga, R.3
Torres De Caballero, O.M.4
Mondragon, A.5
-
49
-
-
0030598829
-
The Spemann organizer signal noggin binds and inactivates bone morphogenetic protein 4
-
ZIMMERMAN L.B., DE JESUS-ESCOBAR J.M., HARLAND R.M.: The Spemann organizer signal noggin binds and inactivates bone morphogenetic protein 4. Cell, 1996, 86, 599-606.
-
(1996)
Cell
, vol.86
, pp. 599-606
-
-
Zimmerman, L.B.1
De Jesus-Escobar, J.M.2
Harland, R.M.3
|