-
1
-
-
0015336856
-
Syndrome of phocomelic diabetic embryopathy (caudal dysplasia)
-
Assemany S, Muzzo S, Gardner L (1972). Syndrome of phocomelic diabetic embryopathy (caudal dysplasia). Am J Dis Child 123:489-491.
-
(1972)
Am J Dis Child
, vol.123
, pp. 489-491
-
-
Assemany, S.1
Muzzo, S.2
Gardner, L.3
-
3
-
-
0028343751
-
Femoral hypoplasia unusual facies syndrome with preaxial polydactyly
-
Baraitser M, Reardon W, Oley C, Fixsen J (1994). Femoral hypoplasia unusual facies syndrome with preaxial polydactyly. Clin Dysmorphol 3:40-45.
-
(1994)
Clin Dysmorphol
, vol.3
, pp. 40-45
-
-
Baraitser, M.1
Reardon, W.2
Oley, C.3
Fixsen, J.4
-
4
-
-
0025017481
-
Diabetes mellitus during pregnancy and the risks for specific birth defects: A population-based case-control study
-
Becerra JE, Khoury MJ, Cordero JF, Erickson JD (1990). Diabetes mellitus during pregnancy and the risks for specific birth defects: a population-based case-control study. Pediatrics 85:1-9.
-
(1990)
Pediatrics
, vol.85
, pp. 1-9
-
-
Becerra, J.E.1
Khoury, M.J.2
Cordero, J.F.3
Erickson, J.D.4
-
5
-
-
0018279418
-
The influence of preconceptional glucose values on the outcome of pregnancy
-
Bergstein N (1978). The influence of preconceptional glucose values on the outcome of pregnancy. Ciba Found Symp 63:255-264.
-
(1978)
Ciba Found Symp
, vol.63
, pp. 255-264
-
-
Bergstein, N.1
-
6
-
-
0019801682
-
Bilateral femoral dysgenesis with micrognathia, cleft palate, anomalies of the spine and pelvis, and foot deformities. Clinical and radiological findings
-
Burck U, Riebel T, Held K, Stoeckenius M (1981). Bilateral femoral dysgenesis with micrognathia, cleft palate, anomalies of the spine and pelvis, and foot deformities. Clinical and radiological findings. Helv Paediatr Acta 36:473-482.
-
(1981)
Helv Paediatr Acta
, vol.36
, pp. 473-482
-
-
Burck, U.1
Riebel, T.2
Held, K.3
Stoeckenius, M.4
-
7
-
-
0021126367
-
The femoral hypoplasia-unusual facies syndrome
-
Burn J, Winter R, Baraitser M, Hall C, Fixsen J (1984). The femoral hypoplasia-unusual facies syndrome. J Med Genet 21:331-340.
-
(1984)
J Med Genet
, vol.21
, pp. 331-340
-
-
Burn, J.1
Winter, R.2
Baraitser, M.3
Hall, C.4
Fixsen, J.5
-
8
-
-
0030761004
-
Bilateral femoral agenesis in femoral facial syndrome in a 19-weekold fetus
-
Campbell F, Vujanić G (1997). Bilateral femoral agenesis in femoral facial syndrome in a 19-weekold fetus. Am J Med Genet 72:315-318.
-
(1997)
Am J Med Genet
, vol.72
, pp. 315-318
-
-
Campbell, F.1
Vujanić, G.2
-
9
-
-
84878775645
-
Femoral hypoplasia-unusual facies syndrome
-
Daentl D, Smith D, Scott C, Hall B, Gooding C (1975). Femoral hypoplasia-unusual facies syndrome. J Pediatr 86:107-111.
-
(1975)
J Pediatr
, vol.86
, pp. 107-111
-
-
Daentl, D.1
Smith, D.2
Scott, C.3
Hall, B.4
Gooding, C.5
-
10
-
-
0022922079
-
Femoral hypoplasia-unusual facies syndrome: Autopsy findings in an unusual case
-
DePalma L, Duray P, Popeo V (1986). Femoral hypoplasia-unusual facies syndrome: autopsy findings in an unusual case. Pediatr Pathol 5:1-8.
-
(1986)
Pediatr Pathol
, vol.5
, pp. 1-8
-
-
DePalma, L.1
Duray, P.2
Popeo, V.3
-
11
-
-
0026212345
-
The femoral hypoplasia syndrome and unusual facies in an infant of a diabetic mother
-
Dumić M, Vuković J, Radica A, Granić M, Car N, Anticević D (1991). The femoral hypoplasia syndrome and unusual facies in an infant of a diabetic mother. Lijec Vjesn 113:324-326.
-
(1991)
Lijec Vjesn
, vol.113
, pp. 324-326
-
-
Dumić, M.1
Vuković, J.2
Radica, A.3
Granić, M.4
Car, N.5
Anticević, D.6
-
12
-
-
4344718554
-
Femoral-facial syndrome with hemifacial microsomia and hypoglossia
-
Düzcan F, Ergin H, Perçin E, Tepeli E, Erkula G (2004). Femoral-facial syndrome with hemifacial microsomia and hypoglossia. Clin Dysmorphol 13:43-44.
-
(2004)
Clin Dysmorphol
, vol.13
, pp. 43-44
-
-
Düzcan, F.1
Ergin, H.2
Perçin, E.3
Tepeli, E.4
Erkula, G.5
-
13
-
-
0018184658
-
Femoral hypoplasia-unusual facies syndrome: A genetic syndrome?
-
Eastman J, Escobar V (1978). Femoral hypoplasia-unusual facies syndrome: a genetic syndrome? Clin Genet 13:72-76.
-
(1978)
Clin Genet
, vol.13
, pp. 72-76
-
-
Eastman, J.1
Escobar, V.2
-
14
-
-
0001275225
-
Congenital skeletal limb deficiencies
-
Frantz CH, O'Rahilly R (1961). Congenital skeletal limb deficiencies. J Bone Joint Surg Am 43:1202-1224.
-
(1961)
J Bone Joint Surg Am
, vol.43
, pp. 1202-1224
-
-
Frantz, C.H.1
O'Rahilly, R.2
-
15
-
-
0029900735
-
Picture of the month. Femoral hypoplasia-unusual facies syndrome
-
Giacoia G, Tunnessen WJ (1996). Picture of the month. Femoral hypoplasia-unusual facies syndrome. Arch Pediatr Adolesc Med 150:761-762.
-
(1996)
Arch Pediatr Adolesc Med
, vol.150
, pp. 761-762
-
-
Giacoia, G.1
Tunnessen, W.J.2
-
17
-
-
0017802244
-
Femoral hypoplasiaunusual facies syndrome, from another viewpoint
-
Gleiser S, Weaver D, Escobar V, Nichols G, Escobedo M (1978). Femoral hypoplasiaunusual facies syndrome, from another viewpoint. Eur J Pediatr 128:1-5.
-
(1978)
Eur J Pediatr
, vol.128
, pp. 1-5
-
-
Gleiser, S.1
Weaver, D.2
Escobar, V.3
Nichols, G.4
Escobedo, M.5
-
19
-
-
0018965915
-
Proximal femoral focal deficiency associated with the Robin anomalad
-
Graviss E, Monteleone P, Wampler L, Silberstein M, Brodeur A (1980). Proximal femoral focal deficiency associated with the Robin anomalad. J Med Genet 17:390-392.
-
(1980)
J Med Genet
, vol.17
, pp. 390-392
-
-
Graviss, E.1
Monteleone, P.2
Wampler, L.3
Silberstein, M.4
Brodeur, A.5
-
20
-
-
0016732695
-
U-shaped palatal defect in the Robin anomalad: Developmental and clinical relevance
-
Hanson J, Smith D (1975). U-shaped palatal defect in the Robin anomalad: developmental and clinical relevance. J Pediatr 87:30-33.
-
(1975)
J Pediatr
, vol.87
, pp. 30-33
-
-
Hanson, J.1
Smith, D.2
-
21
-
-
0030480286
-
Femoral hypoplasia and maternal diabetes: Consider femoral hypoplasia/unusual facies syndrome
-
Hinson R, Miller R, Macri C (1996). Femoral hypoplasia and maternal diabetes: consider femoral hypoplasia/unusual facies syndrome. Am J Perinatol 13:433-436.
-
(1996)
Am J Perinatol
, vol.13
, pp. 433-436
-
-
Hinson, R.1
Miller, R.2
Macri, C.3
-
22
-
-
0016565130
-
Letter: Femoral hypoplasia-unusual facies syndrome
-
Holmes L (1975). Letter: Femoral hypoplasia-unusual facies syndrome. J Pediatr 87:668-669.
-
(1975)
J Pediatr
, vol.87
, pp. 668-669
-
-
Holmes, L.1
-
23
-
-
0015313768
-
The Pierre Robin syndrome: Unusual associated developmental defects
-
Holthusen W (1972). The Pierre Robin syndrome: unusual associated developmental defects. Ann Radiol (Paris) 15:253-262.
-
(1972)
Ann Radiol (Paris)
, vol.15
, pp. 253-262
-
-
Holthusen, W.1
-
24
-
-
0018816850
-
Brief clinical report: Femoral hypoplasia-unusual facies syndrome
-
Hurst D, Johnson D (1980). Brief clinical report: femoral hypoplasia-unusual facies syndrome. Am J Med Genet 5:255-258.
-
(1980)
Am J Med Genet
, vol.5
, pp. 255-258
-
-
Hurst, D.1
Johnson, D.2
-
25
-
-
0009467230
-
Femoral hypoplasia-unusual facies syndrome (FH-UFS): The first report in a sibling pair
-
Inati M, Nores J, Breg W, Al E (1991). Femoral hypoplasia-unusual facies syndrome (FH-UFS): the first report in a sibling pair. Am J Hum Genet 49:142.
-
(1991)
Am J Hum Genet
, vol.49
, pp. 142
-
-
Inati, M.1
Nores, J.2
Breg, W.3
Al, E.4
-
26
-
-
0036278239
-
Airway management in a baby with femoral hypoplasiaunusual facies syndrome
-
Iohom G, Lyons B, Casey W (2002). Airway management in a baby with femoral hypoplasiaunusual facies syndrome. Paediatr Anaesth 12:461-464.
-
(2002)
Paediatr Anaesth
, vol.12
, pp. 461-464
-
-
Iohom, G.1
Lyons, B.2
Casey, W.3
-
27
-
-
0020511169
-
Femoral hypoplasiaunusual facies syndrome in infants of diabetic mothers
-
Johnson J, Carey J, Gooch WR, Petersen J, Beattie J (1983). Femoral hypoplasiaunusual facies syndrome in infants of diabetic mothers. J Pediatr 102:866-872.
-
(1983)
J Pediatr
, vol.102
, pp. 866-872
-
-
Johnson, J.1
Carey, J.2
Gooch, W.R.3
Petersen, J.4
Beattie, J.5
-
28
-
-
33750909282
-
Femoral hypoplasia - unusual facies syndrome
-
Kastanek B, Michael K (2006). Femoral hypoplasia - unusual facies syndrome. J Diagn Med Sonogr 22:391-394.
-
(2006)
J Diagn Med Sonogr
, vol.22
, pp. 391-394
-
-
Kastanek, B.1
Michael, K.2
-
29
-
-
0032840874
-
Diabetic embryopathy
-
Koussef BG (1999). Diabetic embryopathy. Curr Opin Pediatr 11:348-352.
-
(1999)
Curr Opin Pediatr
, vol.11
, pp. 348-352
-
-
Koussef, B.G.1
-
30
-
-
0018853665
-
Dominant inheritance of femoral hypoplasia-unusual facies syndrome
-
Lampert R (1980). Dominant inheritance of femoral hypoplasia-unusual facies syndrome. Clin Genet 17:255-258.
-
(1980)
Clin Genet
, vol.17
, pp. 255-258
-
-
Lampert, R.1
-
31
-
-
0346037178
-
Femoral-facial syndrome with malformations in the central nervous system
-
Leal E, Macias-Gomez N, Rodriguez L, Mercado FM, Barros-Nunez P (2003). Femoral-facial syndrome with malformations in the central nervous system. Clin Imaging 27:23-26.
-
(2003)
Clin Imaging
, vol.27
, pp. 23-26
-
-
Leal, E.1
Macias-Gomez, N.2
Rodriguez, L.3
Mercado, F.M.4
Barros-Nunez, P.5
-
32
-
-
0019779341
-
The femoral hypoplasia-unusual facies syndrome: A genetic entity?
-
Lord J, Beighton P (1981). The femoral hypoplasia-unusual facies syndrome: a genetic entity? Clin Genet 20:267-275.
-
(1981)
Clin Genet
, vol.20
, pp. 267-275
-
-
Lord, J.1
Beighton, P.2
-
33
-
-
0020661609
-
Brief clinical report: Skeletal dysplasia with short, angulated femora (kyphomelic dysplasia)
-
Maclean R, Prater W, Lozzio C (1983). Brief clinical report: skeletal dysplasia with short, angulated femora (kyphomelic dysplasia). Am J Med Genet 14:373-380.
-
(1983)
Am J Med Genet
, vol.14
, pp. 373-380
-
-
Maclean, R.1
Prater, W.2
Lozzio, C.3
-
34
-
-
0018948741
-
The Pierre Robin syndrome associated with femoral dysgenesis
-
Maisels D, Stilwell J (1980). The Pierre Robin syndrome associated with femoral dysgenesis. Br J Plast Surg 33:237-241.
-
(1980)
Br J Plast Surg
, vol.33
, pp. 237-241
-
-
Maisels, D.1
Stilwell, J.2
-
35
-
-
55349089496
-
Potter's syndrome: Chromosome analysis of three cases with Potter's syndrome or related syndromes
-
Passarge E, Sutherland JM (1965). Potter's syndrome: chromosome analysis of three cases with Potter's syndrome or related syndromes. Am J Dis Child 109:80-84.
-
(1965)
Am J Dis Child
, vol.109
, pp. 80-84
-
-
Passarge, E.1
Sutherland, J.M.2
-
36
-
-
0020105890
-
Case report: Femoral hypoplasia - unusual facies syndrome
-
Pitt D, Findlay I, Cole W, Rogers J (1982). Case report: femoral hypoplasia - unusual facies syndrome. Aust Paediatr J 18:63-66.
-
(1982)
Aust Paediatr J
, vol.18
, pp. 63-66
-
-
Pitt, D.1
Findlay, I.2
Cole, W.3
Rogers, J.4
-
37
-
-
33747040862
-
Femoral facial syndrome with bilateral agenesis of femora and preaxial polydactyly of the feet in a Chinese stillborn
-
Poon W, Yuen M, Ng S, Leung Y (2006). Femoral facial syndrome with bilateral agenesis of femora and preaxial polydactyly of the feet in a Chinese stillborn. Clin Imaging 30:357-360.
-
(2006)
Clin Imaging
, vol.30
, pp. 357-360
-
-
Poon, W.1
Yuen, M.2
Ng, S.3
Leung, Y.4
-
38
-
-
0021874279
-
Caudal dysplasia and femoral hypoplasia-unusual facies syndrome: Different manifestations of the same disorder?
-
Riedel F, Froster-Iskenius U (1985). Caudal dysplasia and femoral hypoplasia-unusual facies syndrome: different manifestations of the same disorder? Eur J Pediatr 144:80-82.
-
(1985)
Eur J Pediatr
, vol.144
, pp. 80-82
-
-
Riedel, F.1
Froster-Iskenius, U.2
-
39
-
-
0029058966
-
Femoral-facial syndrome-prenatal diagnosis-autosomal dominant inheritance
-
Robinow M, Sonek J, Buttino L, Veghte A (1995). Femoral-facial syndrome-prenatal diagnosis-autosomal dominant inheritance. Am J Med Genet 57:397-399.
-
(1995)
Am J Med Genet
, vol.57
, pp. 397-399
-
-
Robinow, M.1
Sonek, J.2
Buttino, L.3
Veghte, A.4
-
40
-
-
0030041807
-
Femoral hypoplasia-unusual facies syndrome with bifid hallux, absent tibia, and macrophallus: A report of a Bedouin baby
-
Sabry M, Obenbergerova D, Al-Sawan R, Saleh Q, Farah S, Al-Awadi S, Farag T (1996). Femoral hypoplasia-unusual facies syndrome with bifid hallux, absent tibia, and macrophallus: a report of a Bedouin baby. J Med Genet 33:165-167.
-
(1996)
J Med Genet
, vol.33
, pp. 165-167
-
-
Sabry, M.1
Obenbergerova, D.2
Al-Sawan, R.3
Saleh, Q.4
Farah, S.5
Al-Awadi, S.6
Farag, T.7
-
41
-
-
0019819956
-
Pierre Robin syndrome associated with hypoplastic femora-another case report
-
Sandison R, Johnson J (1981). Pierre Robin syndrome associated with hypoplastic femora-another case report. Br J Plast Surg 34:309-311.
-
(1981)
Br J Plast Surg
, vol.34
, pp. 309-311
-
-
Sandison, R.1
Johnson, J.2
-
43
-
-
0027428564
-
Femoral hypoplasia-unusual facies syndrome: Prenatal ultrasonographic observations
-
Tadmor O, Hammerman C, Rabinowitz R, Fisher D, Itzchaki M, Aboulafia Y, Diamant Y (1993). Femoral hypoplasia-unusual facies syndrome: prenatal ultrasonographic observations. Fetal Diagn Ther 8:279-284.
-
(1993)
Fetal Diagn Ther
, vol.8
, pp. 279-284
-
-
Tadmor, O.1
Hammerman, C.2
Rabinowitz, R.3
Fisher, D.4
Itzchaki, M.5
Aboulafia, Y.6
Diamant, Y.7
-
44
-
-
0024824072
-
Femoral hypoplasia-unusual facies syndrome
-
Trabelsi M, Monastiri K, Hammami A, Touzi C, Ben Hariz M, Gharbi H, Bennaceur B (1989). Femoral hypoplasia-unusual facies syndrome. Ann Pediatr (Paris) 36:693-696.
-
(1989)
Ann Pediatr (Paris)
, vol.36
, pp. 693-696
-
-
Trabelsi, M.1
Monastiri, K.2
Hammami, A.3
Touzi, C.4
Ben Hariz, M.5
Gharbi, H.6
Bennaceur, B.7
-
45
-
-
0030953699
-
Autopsy, radiographic, and prenatal ultrasonographic examination of a stillborn fetus with femoral facial syndrome
-
Urban J, Ramus R, Stannard M, Rogers B (1997). Autopsy, radiographic, and prenatal ultrasonographic examination of a stillborn fetus with femoral facial syndrome. Am J Med Genet 71:76-79.
-
(1997)
Am J Med Genet
, vol.71
, pp. 76-79
-
-
Urban, J.1
Ramus, R.2
Stannard, M.3
Rogers, B.4
-
46
-
-
0036597568
-
Additional malformations in femoral hypoplasia: Unusual facies syndrome
-
Verma A, Jain N, Jain K (2002). Additional malformations in femoral hypoplasia: unusual facies syndrome. Indian J Pediatr 69:531-532.
-
(2002)
Indian J Pediatr
, vol.69
, pp. 531-532
-
-
Verma, A.1
Jain, N.2
Jain, K.3
-
47
-
-
0015083451
-
Pierre Robin syndrome in association with combined congenital lengthening and shortening of the long bones. Case report
-
Walden R, Logosso R, Brennan L (1971). Pierre Robin syndrome in association with combined congenital lengthening and shortening of the long bones. Case report. Plast Reconstr Surg 48:80-82.
-
(1971)
Plast Reconstr Surg
, vol.48
, pp. 80-82
-
-
Walden, R.1
Logosso, R.2
Brennan, L.3
-
48
-
-
0014776727
-
A syndrome of congenital malformations possibly due to maternal diabetes
-
Williamson D (1970). A syndrome of congenital malformations possibly due to maternal diabetes. Dev Med Child Neurol 12:145-152.
-
(1970)
Dev Med Child Neurol
, vol.12
, pp. 145-152
-
-
Williamson, D.1
-
49
-
-
0030665724
-
Maternal diabetes and fetal malformations: A case associating cardiovascular, facial and skeletal malformations
-
Ziereisen F, Courtens W, Clercx A, Perlmutter N (1997). Maternal diabetes and fetal malformations: a case associating cardiovascular, facial and skeletal malformations. Pediatr Radiol 27:945-947.
-
(1997)
Pediatr Radiol
, vol.27
, pp. 945-947
-
-
Ziereisen, F.1
Courtens, W.2
Clercx, A.3
Perlmutter, N.4
|