-
1
-
-
0021683829
-
Congenital heart disease and twinning
-
Roma
-
Burn J, Corney G. 1984. Congenital heart disease and twinning. Acta Genet Med Gemellol (Roma) 33:61-69.
-
(1984)
Acta Genet Med Gemellol
, vol.33
, pp. 61-69
-
-
Burn, J.1
Corney, G.2
-
3
-
-
0029448485
-
Hypertelorism: Interorbital growth, measurements, and pathogenetic considerations
-
Cohen MM, Richieri-Costa A, Guion-Almeida ML, Saavedra D. 1995. Hypertelorism: Interorbital growth, measurements, and pathogenetic considerations. J Oral Maxillofac Surg 24:387-395.
-
(1995)
J Oral Maxillofac Surg
, vol.24
, pp. 387-395
-
-
Cohen, M.M.1
Richieri-Costa, A.2
Guion-Almeida, M.L.3
Saavedra, D.4
-
4
-
-
0023203496
-
Pathogenesis of median facial clefts in mice treated with methotrexate
-
Darab DJ, Minkoff R, Sciote J, Sulik KK. 1987. Pathogenesis of median facial clefts in mice treated with methotrexate. Teratology 36:77-86.
-
(1987)
Teratology
, vol.36
, pp. 77-86
-
-
Darab, D.J.1
Minkoff, R.2
Sciote, J.3
Sulik, K.K.4
-
5
-
-
13344259999
-
A comprehensive genetic map of the human genome based on 5,264 microsatellites
-
Dib C, Faure S, Fizames C, Samson D, Drouot N, Vignal A, Millasseau P, Marc S, Hazan J, Seboun E, Lathrop M, Gyapay G, Morissette J, Weissenbach J. 1996. A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature 380:152-154.
-
(1996)
Nature
, vol.380
, pp. 152-154
-
-
Dib, C.1
Faure, S.2
Fizames, C.3
Samson, D.4
Drouot, N.5
Vignal, A.6
Millasseau, P.7
Marc, S.8
Hazan, J.9
Seboun, E.10
Lathrop, M.11
Gyapay, G.12
Morissette, J.13
Weissenbach, J.14
-
6
-
-
0027182358
-
Frontonasal malformation in two successive generations
-
Fryburg JS, Persing JA, Lin KY. 1993. Frontonasal malformation in two successive generations. Am J Med Genet 46:712-714.
-
(1993)
Am J Med Genet
, vol.46
, pp. 712-714
-
-
Fryburg, J.S.1
Persing, J.A.2
Lin, K.Y.3
-
7
-
-
0003868876
-
Frontonasal malformation (frontonasal dysplasia, median cleft face syndrome)
-
Oxford: Oxford University Press
-
Gorlin RJ, Cohen MM Jr, Hennekam RCM. 2001. Frontonasal malformation (frontonasal dysplasia, median cleft face syndrome). In: Syndromes of the head and neck. Oxford: Oxford University Press, pp 977-981.
-
(2001)
Syndromes of the Head and Neck
, pp. 977-981
-
-
Gorlin, R.J.1
Cohen Jr., M.M.2
Hennekam, R.C.M.3
-
9
-
-
0041828261
-
Twinning
-
Hall JG. 2003. Twinning. Lancet 362:735-743.
-
(2003)
Lancet
, vol.362
, pp. 735-743
-
-
Hall, J.G.1
-
10
-
-
0037621688
-
A zone of frontonasal ectoderm regulates patterning and growth in the face
-
Hu D, Marcucio RS, Helms JA. 2003. A zone of frontonasal ectoderm regulates patterning and growth in the face. Development 130:1749-1758.
-
(2003)
Development
, vol.130
, pp. 1749-1758
-
-
Hu, D.1
Marcucio, R.S.2
Helms, J.A.3
-
11
-
-
0032231374
-
A comprehensive screen for TWIST mutations in patients with craniosynostosis identifies a new microdeletion syndrome of chromosome band 7p21.1
-
Johnson D, Horsley SW, Moloney DM, Oldridge M, Twigg SR, Walsh S, Barrow M, Njolstad PR, Kunz J, Ashworth GJ, Wall SA, Kearney L, Wilkie AOM. 1998. A comprehensive screen for TWIST mutations in patients with craniosynostosis identifies a new microdeletion syndrome of chromosome band 7p21.1. Am J Hum Genet 63:1282-1293.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 1282-1293
-
-
Johnson, D.1
Horsley, S.W.2
Moloney, D.M.3
Oldridge, M.4
Twigg, S.R.5
Walsh, S.6
Barrow, M.7
Njolstad, P.R.8
Kunz, J.9
Ashworth, G.J.10
Wall, S.A.11
Kearney, L.12
Wilkie, A.O.M.13
-
12
-
-
0029006411
-
Prenatal craniofacial development: New insights on normal and abnormal mechanisms
-
Johnston MC, Bronsky PT. 1995. Prenatal craniofacial development: New insights on normal and abnormal mechanisms. Crit Rev Oral Biol Med 6:25-79.
-
(1995)
Crit Rev Oral Biol Med
, vol.6
, pp. 25-79
-
-
Johnston, M.C.1
Bronsky, P.T.2
-
13
-
-
0026512102
-
The cyclops and the mermaid: An epidemiological study of two types of rare malformation
-
Kallen B, Castilla EE, Lancaster PA, Mutchinick O, Knudsen LB, Martinez-Frias ML, Mastroiacovo P, Robert E. 1992. The cyclops and the mermaid: An epidemiological study of two types of rare malformation. J Med Genet 29:30-35.
-
(1992)
J Med Genet
, vol.29
, pp. 30-35
-
-
Kallen, B.1
Castilla, E.E.2
Lancaster, P.A.3
Mutchinick, O.4
Knudsen, L.B.5
Martinez-Frias, M.L.6
Mastroiacovo, P.7
Robert, E.8
-
15
-
-
0017259818
-
Ultrasonic assessment of the high rate of human multiple pregnancy in the first trimester
-
Levi S. 1976. Ultrasonic assessment of the high rate of human multiple pregnancy in the first trimester. J Clin Ultrasound 4:3-5.
-
(1976)
J Clin Ultrasound
, vol.4
, pp. 3-5
-
-
Levi, S.1
-
16
-
-
0030049310
-
Some causes of genotypic and phenotypic discordance in monozygotic twin pairs
-
Machin GA. 1996. Some causes of genotypic and phenotypic discordance in monozygotic twin pairs. Am J Med Genet 61:216-228.
-
(1996)
Am J Med Genet
, vol.61
, pp. 216-228
-
-
Machin, G.A.1
-
17
-
-
0019762581
-
Malformations unique to the twinning process
-
Gedda L, Parisi P, Nance WE, editors. New York: Alan R. Liss, Inc.
-
Nance WE. 1981. Malformations unique to the twinning process. In: Gedda L, Parisi P, Nance WE, editors. Twin research 3: Twin biology and multiple pregnancy. New York: Alan R. Liss, Inc., pp 123-133.
-
(1981)
Twin Research 3: Twin Biology and Multiple Pregnancy
, pp. 123-133
-
-
Nance, W.E.1
-
18
-
-
0022411559
-
Etiology of ventricular septal defects: An epidemiologic approach
-
Newman TB. 1985. Etiology of ventricular septal defects: An epidemiologic approach. Pediatrics 76:741-749.
-
(1985)
Pediatrics
, vol.76
, pp. 741-749
-
-
Newman, T.B.1
-
19
-
-
0031671048
-
Congenital anomalies in the teatological collection of the Museum Vrolik in Amsterdam, the Netherlands. V: Conjoined and acardiac twins
-
Ostra RJ, Balijet B, Verbeeten BW, Hennekam RC. 1998. Congenital anomalies in the teatological collection of the Museum Vrolik in Amsterdam, The Netherlands. V: Conjoined and acardiac twins. Am J Med Genet 80:74-89.
-
(1998)
Am J Med Genet
, vol.80
, pp. 74-89
-
-
Ostra, R.J.1
Balijet, B.2
Verbeeten, B.W.3
Hennekam, R.C.4
-
20
-
-
0041821560
-
Otocephaly and holoprosencephaly in only one monozygotic twin
-
Reinecke P, Figge C, Majewski F, Borchard F. 2003. Otocephaly and holoprosencephaly in only one monozygotic twin. Am J Med Genet 119A:395-396.
-
(2003)
Am J Med Genet
, vol.119 A
, pp. 395-396
-
-
Reinecke, P.1
Figge, C.2
Majewski, F.3
Borchard, F.4
-
21
-
-
0019828855
-
Frontonasal dysplasia as an expression of holoprosencephaly
-
Roubicek M, Spranger J, Wende S. 1981. Frontonasal dysplasia as an expression of holoprosencephaly. Eur J Pediatr 137:229-231.
-
(1981)
Eur J Pediatr
, vol.137
, pp. 229-231
-
-
Roubicek, M.1
Spranger, J.2
Wende, S.3
-
23
-
-
0023898135
-
Frontonasal malformation as a field defect and in syndromic associations
-
Sedano HO, Gorlin RJ. 1988. Frontonasal malformation as a field defect and in syndromic associations. Oral Surg Oral Med Oral Pathol 65:704-710.
-
(1988)
Oral Surg Oral Med Oral Pathol
, vol.65
, pp. 704-710
-
-
Sedano, H.O.1
Gorlin, R.J.2
-
25
-
-
0034071416
-
Central nervous system in twin reversed arterial perfusion sequence with special reference to examination of the brain in acardius anceps
-
Sergi C, Schmitt HP. 2000. Central nervous system in twin reversed arterial perfusion sequence with special reference to examination of the brain in acardius anceps. Teratology 61:284-290.
-
(2000)
Teratology
, vol.61
, pp. 284-290
-
-
Sergi, C.1
Schmitt, H.P.2
|