-
1
-
-
0010742668
-
Nuclear sex and genital malformations in 48 cases of renal agenesis, with especial reference to nonspecific female pseudohermaphroditism
-
CARPENTIER R.J., POTTER E.L.: Nuclear sex and genital malformations in 48 cases of renal agenesis, with especial reference to nonspecific female pseudohermaphroditism. Am. J. Obstet. Gynecol., 1959, 78, 235-258.
-
(1959)
Am. J. Obstet. Gynecol.
, vol.78
, pp. 235-258
-
-
Carpentier, R.J.1
Potter, E.L.2
-
2
-
-
0027052344
-
VATER/VACTERL association: Clinical variability and expanding phenotype including laryngeal stenosis
-
CORSELLO G., MARESI E., CORRAO A.M., DIMITA U., LO CASCIO M., CAMMARATA M., GIUFFRE L.: VATER/VACTERL association: clinical variability and expanding phenotype including laryngeal stenosis. Am. J. Med. Genet., 1992, 44, 813-815.
-
(1992)
Am. J. Med. Genet.
, vol.44
, pp. 813-815
-
-
Corsello, G.1
Maresi, E.2
Corrao, A.M.3
Dimita, U.4
Lo Cascio, M.5
Cammarata, M.6
Giuffre, L.7
-
3
-
-
0021741030
-
The Potter sequence: A clinical analysis of 80 cases
-
CURRY C.J.R., JENSEN K., HOLLAND J., MILLER L., HALL B.D.: The Potter sequence: a clinical analysis of 80 cases. Am. J. Med. Genet., 1984, 79, 679-702.
-
(1984)
Am. J. Med. Genet.
, vol.79
, pp. 679-702
-
-
Curry, C.J.R.1
Jensen, K.2
Holland, J.3
Miller, L.4
Hall, B.D.5
-
4
-
-
0026606606
-
Syndrome de Prune Belly. A propos d'un cas de récurrence
-
DARMON J.C., JANKY E., COUCHY B.: Syndrome de Prune Belly. A propos d'un cas de récurrence. Rev. Fr. Gynecol. Obstet., 1992, 87, 151-154.
-
(1992)
Rev. Fr. Gynecol. Obstet.
, vol.87
, pp. 151-154
-
-
Darmon, J.C.1
Janky, E.2
Couchy, B.3
-
5
-
-
0001302731
-
From the mermaid to anal imperforation: The syndrome of caudal regression
-
DUHAMEL B.: From the mermaid to anal imperforation: the syndrome of caudal regression. Arch. Dis. Child., 1961, 36, 152-155.
-
(1961)
Arch. Dis. Child.
, vol.36
, pp. 152-155
-
-
Duhamel, B.1
-
6
-
-
0018332940
-
The MURCS association: Müllerian duct aplasia, renal aplasia, and cervicothoracic dysplasia
-
DUNCAN P.P., SHAPIRO L.R., SANGEL J.J., KLEIN R.M. ADDONIZIO J.C.: The MURCS association: Müllerian duct aplasia, renal aplasia, and cervicothoracic dysplasia. J. Pediarr., 1979, 95, 399-402.
-
(1979)
J. Pediarr.
, vol.95
, pp. 399-402
-
-
Duncan, P.P.1
Shapiro, L.R.2
Sangel, J.J.3
Klein, R.M.4
Addonizio, J.C.5
-
7
-
-
0026701702
-
Patterns of acrorenal malformation associations
-
EVANS J.A., VITEZ M., CZEIZEL A.: Patterns of acrorenal malformation associations. Am. J. Med. Genet., 1992, 44, 413-419.
-
(1992)
Am. J. Med. Genet.
, vol.44
, pp. 413-419
-
-
Evans, J.A.1
Vitez, M.2
Czeizel, A.3
-
8
-
-
0016574647
-
Potters syndrome - Nonrenal features induced by oligamnios
-
FANTEL A., SHEPARD T.: Potters syndrome - nonrenal features induced by oligamnios. Am. J. Dis. Child., 1975, 129, 1346-1347.
-
(1975)
Am. J. Dis. Child.
, vol.129
, pp. 1346-1347
-
-
Fantel, A.1
Shepard, T.2
-
9
-
-
0027512089
-
Familial segregation of cervical ribs, Sprengel anomaly, preaxial polydactyly, anal atresia, and urethral obstruction: A new syndrome?
-
FRYDMAN M., COHEN H.A., ASHKENAZI A., VARSANO I.: Familial segregation of cervical ribs, Sprengel anomaly, preaxial polydactyly, anal atresia, and urethral obstruction: a new syndrome? Am. J. Med. Genet., 1993, 45, 717-720.
-
(1993)
Am. J. Med. Genet.
, vol.45
, pp. 717-720
-
-
Frydman, M.1
Cohen, H.A.2
Ashkenazi, A.3
Varsano, I.4
-
10
-
-
0027418519
-
Diagnostic positif du syndrome de Potter par i'échographie. A propos d'une observation
-
GARBA H., DACHIVRE J., BROUSSARD P.: Diagnostic positif du syndrome de Potter par i'échographie. A propos d'une observation. Rev. Fr. Gvnecol. Obstet., 1993, 88, 156-161.
-
(1993)
Rev. Fr. Gvnecol. Obstet.
, vol.88
, pp. 156-161
-
-
Garba, H.1
Dachivre, J.2
Broussard, P.3
-
11
-
-
0023821757
-
Das Prune-Belly-Syndrom. Prenatale Diagnose und Geburtshilfliches Vorgehen
-
GNIRS J., BOOS R., WALDHERR R., SCHMIDT W.: Das Prune-Belly-Syndrom. Prenatale Diagnose und Geburtshilfliches Vorgehen. Z. Geburishilfe Perinatol., 1988, 192, 114-121.
-
(1988)
Z. Geburishilfe Perinatol.
, vol.192
, pp. 114-121
-
-
Gnirs, J.1
Boos, R.2
Waldherr, R.3
Schmidt, W.4
-
12
-
-
0027573023
-
Megalourethra associated with prune-belly syndrome
-
GOKALP A., GULTEKIN E.Y.: Megalourethra associated with prune-belly syndrome. Turk. J. Pediatr., 1993, 35, 151-153.
-
(1993)
Turk. J. Pediatr.
, vol.35
, pp. 151-153
-
-
Gokalp, A.1
Gultekin, E.Y.2
-
13
-
-
0027251892
-
Congenital microgastria in an infant with the VACTERL association
-
HASEGAWA S., KOHNO S., TAMURA K., URUSHIHARA N.: Congenital microgastria in an infant with the VACTERL association. J. Pediatr. Surg., 1993, 28, 782-784.
-
(1993)
J. Pediatr. Surg.
, vol.28
, pp. 782-784
-
-
Hasegawa, S.1
Kohno, S.2
Tamura, K.3
Urushihara, N.4
-
14
-
-
0020623203
-
A population study of the VACTERL association: Evidence for its etiologic heterogeneity
-
KHOURY M.J., LORDERO J.F., GREENBERG F., JAMES L.J., ERICKSON J.D.: A population study of the VACTERL association: Evidence for its etiologic heterogeneity. Pediatrics, 1983, 71, 815-820.
-
(1983)
Pediatrics
, vol.71
, pp. 815-820
-
-
Khoury, M.J.1
Lordero, J.F.2
Greenberg, F.3
James, L.J.4
Erickson, J.D.5
-
15
-
-
0004293174
-
-
New York, Edinburgh, London, Melbourne, Tokyo, Churchill Livingstone, Inc.
-
LARSEN W.J.: Human Embryology. New York, Edinburgh, London, Melbourne, Tokyo, Churchill Livingstone, Inc., 1993.
-
(1993)
Human Embryology
-
-
Larsen, W.J.1
-
16
-
-
0018670818
-
Siblings with prune belly syndrome and associated pulmonic stenosis, mental retardation and deafness
-
LOCKHART J.I., REEVE H.R., BREBAEL J.J., KRUEGER R.P.: Siblings with prune belly syndrome and associated pulmonic stenosis, mental retardation and deafness. Urology, 1979, 14, 140-142.
-
(1979)
Urology
, vol.14
, pp. 140-142
-
-
Lockhart, J.I.1
Reeve, H.R.2
Brebael, J.J.3
Krueger, R.P.4
-
17
-
-
0018934204
-
Female pseudohermaphroditism and associated anomalies
-
LUBINSKY M.S.: Female pseudohermaphroditism and associated anomalies. Am. J. Med. Genet., 1980, 6, 123-136.
-
(1980)
Am. J. Med. Genet.
, vol.6
, pp. 123-136
-
-
Lubinsky, M.S.1
-
18
-
-
0042351971
-
Different clusters within the VATER association distinguished through cardiac defects: Possible effects of teratologic timing
-
LUBINSKY M.S., MOESCHLER J.: Different clusters within the VATER association distinguished through cardiac defects: possible effects of teratologic timing. Dysmorphol. Clin. Genet., 1987, 1, 80-82.
-
(1987)
Dysmorphol. Clin. Genet.
, vol.1
, pp. 80-82
-
-
Lubinsky, M.S.1
Moeschler, J.2
-
19
-
-
0026894392
-
MURCS association - A review of 7 cases
-
MAHAJAN P., KHER A., KHUNGAR A., BHAT M., SANKLECHA M., BHARUCHA B.A.: MURCS association - A review of 7 cases. J. Postgrad. Med., 1992, 38, 109-111.
-
(1992)
J. Postgrad. Med.
, vol.38
, pp. 109-111
-
-
Mahajan, P.1
Kher, A.2
Khungar, A.3
Bhat, M.4
Sanklecha, M.5
Bharucha, B.A.6
-
20
-
-
0026524452
-
Case of multivertebral anomalies, cloacal dysgenesis, and other anomalies presenting prenatally as cystic kidneys
-
MURR M.M., WAZIRI M.H., SCHELPER R.L., ABU-YOUSELF M.: Case of multivertebral anomalies, cloacal dysgenesis, and other anomalies presenting prenatally as cystic kidneys. Am. J. Med. Genet., 1992, 42, 761-765.
-
(1992)
Am. J. Med. Genet.
, vol.42
, pp. 761-765
-
-
Murr, M.M.1
Waziri, M.H.2
Schelper, R.L.3
Abu-Youself, M.4
-
21
-
-
0019972854
-
The developmental field concept in clinical genetics
-
OPITZ J.M.: The developmental field concept in clinical genetics. J. Pediatr., 1982, 101, 805-809.
-
(1982)
J. Pediatr.
, vol.101
, pp. 805-809
-
-
Opitz, J.M.1
-
22
-
-
0021801019
-
Editorial comment: The developmental field concept
-
OPITZ J.M.: Editorial comment: The developmental field concept. Am. J. Med. Genet., 1985, 21, 1-11.
-
(1985)
Am. J. Med. Genet.
, vol.21
, pp. 1-11
-
-
Opitz, J.M.1
-
23
-
-
0026778516
-
VACTERL or MURCS association in a girl with neurenteric cyst and identical thoracic malformations in the father: A case of gonosomal mosaïcism?
-
ORSTAVIK K.H., STEEN-JOHNSEN J., FOERSTER A., FJELD T., SKULLERUD K., LIE S.O.: VACTERL or MURCS association in a girl with neurenteric cyst and identical thoracic malformations in the father: a case of gonosomal mosaïcism? Am. J. Med. Genet., 1992, 43, 1035-1038.
-
(1992)
Am. J. Med. Genet.
, vol.43
, pp. 1035-1038
-
-
Orstavik, K.H.1
Steen-Johnsen, J.2
Foerster, A.3
Fjeld, T.4
Skullerud, K.5
Lie, S.O.6
-
24
-
-
0027990747
-
Konkordanz von Prune-Belly-Syndrom und VACTERL association
-
OZTURK B., WEBER H.P., GANZ A.: Konkordanz von Prune-Belly-Syndrom und VACTERL association. Klin. Paediatr., 1994, 206, 406-409.
-
(1994)
Klin. Paediatr.
, vol.206
, pp. 406-409
-
-
Ozturk, B.1
Weber, H.P.2
Ganz, A.3
-
25
-
-
0026516399
-
MURCS association and hypothalamic anovulation
-
PABLO MENDEZ J., OROZCO M., IVAN RUIZ A., OROZCO E., DIAZ L.: MURCS association and hypothalamic anovulation. Rev. Invest. Clin., 1992, 44, 115-121.
-
(1992)
Rev. Invest. Clin.
, vol.44
, pp. 115-121
-
-
Pablo Mendez, J.1
Orozco, M.2
Ivan Ruiz, A.3
Orozco, E.4
Diaz, L.5
-
26
-
-
0015319647
-
Twins with congenital deficiency of abdominal musculature
-
PETERSEN D.S., FISH L., CASS A.S.: Twins with congenital deficiency of abdominal musculature. J. Urol., 1972, 107, 670-672.
-
(1972)
J. Urol.
, vol.107
, pp. 670-672
-
-
Petersen, D.S.1
Fish, L.2
Cass, A.S.3
-
27
-
-
84872623412
-
Facial characteristics of infants with bilateral renal agenesis
-
POTTER E.L.: Facial characteristics of infants with bilateral renal agenesis. Am. J. Obstet. Gynecol., 1946, 51, 885-888.
-
(1946)
Am. J. Obstet. Gynecol.
, vol.51
, pp. 885-888
-
-
Potter, E.L.1
-
28
-
-
0023901906
-
Interstitial deletion of chromosome 1 [del(1)(Q25Q32)] in an infant with prune belly sequence
-
SCARBROUGH P.R., FILES B., CARROLL A.J., QUINLAN R.W., FINLEY S.C., FINLEY W.H.: Interstitial deletion of chromosome 1 [del(1)(Q25Q32)] in an infant with prune belly sequence. Prenat. Diagn., 1988, 8, 169-174.
-
(1988)
Prenat. Diagn.
, vol.8
, pp. 169-174
-
-
Scarbrough, P.R.1
Files, B.2
Carroll, A.J.3
Quinlan, R.W.4
Finley, S.C.5
Finley, W.H.6
-
29
-
-
0018692738
-
Monozygotic twinning and structural defects
-
SCHINZEL A.A.G.L., SMITH D.W., MILLER J.R.: Monozygotic twinning and structural defects. J. Pediatr., 1979, 95, 921-930.
-
(1979)
J. Pediatr.
, vol.95
, pp. 921-930
-
-
Schinzel, A.A.G.L.1
Smith, D.W.2
Miller, J.R.3
-
30
-
-
0013969857
-
An XX sex chromosome complement in an infant having male-type external genitals, renal agenesis, and other anomalies
-
SCHLEGEL R.J., ASPILLAGA M.J., NEU R.L., CARNEIRO-LEAO J., GARDNER L.I.: An XX sex chromosome complement in an infant having male-type external genitals, renal agenesis, and other anomalies. J. Pediatr., 1966, 69, 812-814.
-
(1966)
J. Pediatr.
, vol.69
, pp. 812-814
-
-
Schlegel, R.J.1
Aspillaga, M.J.2
Neu, R.L.3
Carneiro-Leao, J.4
Gardner, L.I.5
-
31
-
-
0028099471
-
Pathogenesis of the prune belly syndrome
-
STEPHENS F.D., GUPTA D.: Pathogenesis of the prune belly syndrome. J. Urol., 1994, 152, 2328-2331.
-
(1994)
J. Urol.
, vol.152
, pp. 2328-2331
-
-
Stephens, F.D.1
Gupta, D.2
-
32
-
-
0016279187
-
Extending the scope of the VATER association: Definition of the VATER syndrome
-
TEMTAMY S.A., MILLER J.D.: Extending the scope of the VATER association: Definition of the VATER syndrome. J. Pediatr., 1974, 85, 345-349.
-
(1974)
J. Pediatr.
, vol.85
, pp. 345-349
-
-
Temtamy, S.A.1
Miller, J.D.2
-
33
-
-
0016212101
-
Oligohydramnios. The cause of the non-renal features of Potter's syndrome, including pulmonary hypoplasia
-
THOMAS I.T., SMITH D.W.: Oligohydramnios. the cause of the non-renal features of Potter's syndrome, including pulmonary hypoplasia. J. Pediatr., 1974, 84, 811-814.
-
(1974)
J. Pediatr.
, vol.84
, pp. 811-814
-
-
Thomas, I.T.1
Smith, D.W.2
-
34
-
-
0022640393
-
The VATER association: Analysis of 46 patients
-
WEAVER D.D., MAPSTONE C.L., YU P.L.: The VATER association: analysis of 46 patients. Am. J. Dis. Child., 1986, 140, 225-229.
-
(1986)
Am. J. Dis. Child.
, vol.140
, pp. 225-229
-
-
Weaver, D.D.1
Mapstone, C.L.2
Yu, P.L.3
-
35
-
-
0020400586
-
Prune belly syndrome - Report of 47 cases
-
WOODHOUSE C.R.J., RANSLEY P.G., INNES-WILLIAMS D.: Prune belly syndrome - Report of 47 cases. Arch. Dis. Child., 1982, 57, 856-859.
-
(1982)
Arch. Dis. Child.
, vol.57
, pp. 856-859
-
-
Woodhouse, C.R.J.1
Ransley, P.G.2
Innes-Williams, D.3
-
36
-
-
8244255815
-
Incidence and genetics of congenital malformations
-
Brock D.J.H., Rodeck C.H. and Ferguson-Smith M.A. (eds). Edinburgh, London, Madrid, Melbourne, New york, Tokyo, Churchill Livingstone, Inc.
-
YOUNG I.D.: Incidence and genetics of congenital malformations. In: Prenatal Diagnosis and Screening. Brock D.J.H., Rodeck C.H. and Ferguson-Smith M.A. (eds). Edinburgh, London, Madrid, Melbourne, New york, Tokyo, Churchill Livingstone, Inc., 1992, 171-187.
-
(1992)
Prenatal Diagnosis and Screening
, pp. 171-187
-
-
Young, I.D.1
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