-
1
-
-
0029815064
-
Sotos syndrome: Evolution of facial phenotype. Subjective and objective assessment
-
Allanson JE, Cole TRP (1996): Sotos syndrome: Evolution of facial phenotype. Subjective and objective assessment. Am J Med Genet 65:13-20.
-
(1996)
Am J Med Genet
, vol.65
, pp. 13-20
-
-
Allanson, J.E.1
Cole, T.R.P.2
-
2
-
-
0021722979
-
Weaver-Smith syndrome: A case study with long-term follow-up
-
Amir N, Gross-Kieselstein E, Hirsch H, Lax E, Silverberg-Shale VR (1984): Weaver-Smith syndrome: A case study with long-term follow-up. AJDC 138:1113-1117.
-
(1984)
AJDC
, vol.138
, pp. 1113-1117
-
-
Amir, N.1
Gross-Kieselstein, E.2
Hirsch, H.3
Lax, E.4
Silverberg-Shale, V.R.5
-
3
-
-
0022636447
-
Further delineation of Weaver syndrome
-
Ardinger HH, Hanson JW, Harrod MJE, Cohen MM Jr, Tibbles JAR, Welch JP, Young-Wee T, Sommer A, Goldberg R, Shprintzen RJ, Sidoti EJ, Leichtman LG, Hoyme HE (1986): Further delineation of Weaver syndrome. J Pediatr 108:228-235.
-
(1986)
J Pediatr
, vol.108
, pp. 228-235
-
-
Ardinger, H.H.1
Hanson, J.W.2
Harrod, M.J.E.3
Cohen Jr., M.M.4
Tibbles, J.A.R.5
Welch, J.P.6
Young-Wee, T.7
Sommer, A.8
Goldberg, R.9
Shprintzen, R.J.10
Sidoti, E.J.11
Leichtman, L.G.12
Hoyme, H.E.13
-
4
-
-
0021923751
-
Familial Sotos syndrome (cerebral gigantism): Craniofacial and psychological characteristics
-
Bale AE, Drum MA, Parry DM, Mulvihill JJ (1985): Familial Sotos syndrome (cerebral gigantism): Craniofacial and psychological characteristics. Am J Med Genet 20:613-624.
-
(1985)
Am J Med Genet
, vol.20
, pp. 613-624
-
-
Bale, A.E.1
Drum, M.A.2
Parry, D.M.3
Mulvihill, J.J.4
-
5
-
-
33749690572
-
An unusual case of early overgrowth and congenital anomalies - The Weaver syndrome
-
abstract 222
-
Bayley-Wilson JE, Shapira E, Blitzer MG, Braverman N (1983): An unusual case of early overgrowth and congenital anomalies - the Weaver syndrome (abstract 222). Am J Hum Genet 35:75A.
-
(1983)
Am J Hum Genet
, vol.35
-
-
Bayley-Wilson, J.E.1
Shapira, E.2
Blitzer, M.G.3
Braverman, N.4
-
6
-
-
0022573461
-
Cerebral gigantism (Sotos syndrome) in two patients with fragile (X) syndrome
-
Beemer FA, Veenema H, de Pater JM (1986): Cerebral gigantism (Sotos syndrome) in two patients with fragile (X) syndrome. Am J Med Genet 23:221-226.
-
(1986)
Am J Med Genet
, vol.23
, pp. 221-226
-
-
Beemer, F.A.1
Veenema, H.2
De Pater, J.M.3
-
8
-
-
0014713879
-
Cerebral gigantism: Concentrations of amino acids in plasma and muscle
-
Bejar RL, Smith GF, Park SM, Spellacy WN, Wolfson SL, Nyhan WL (1970): Cerebral gigantism: Concentrations of amino acids in plasma and muscle. J Pediatr 76:105-111.
-
(1970)
J Pediatr
, vol.76
, pp. 105-111
-
-
Bejar, R.L.1
Smith, G.F.2
Park, S.M.3
Spellacy, W.N.4
Wolfson, S.L.5
Nyhan, W.L.6
-
9
-
-
0019162408
-
Sotos syndrome in two brothers
-
Boman H, Nilsson D (1980): Sotos syndrome in two brothers. Clin Genet 18:421-427.
-
(1980)
Clin Genet
, vol.18
, pp. 421-427
-
-
Boman, H.1
Nilsson, D.2
-
10
-
-
0017878955
-
Accélération du developpement postnatal
-
Bosch-Banyeras JM, Salcedo S, Lucaya J, Laverde R, Boronat M, Marti-Henneberg C (1978): Accélération du developpement postnatal. Arch Fr Pédiatr 35:177-183.
-
(1978)
Arch Fr Pédiatr
, vol.35
, pp. 177-183
-
-
Bosch-Banyeras, J.M.1
Salcedo, S.2
Lucaya, J.3
Laverde, R.4
Boronat, M.5
Marti-Henneberg, C.6
-
11
-
-
0021959504
-
Metacarpophalangeal pattern profile analysis in Sotos syndrome
-
Butler MG, Meany FJ, Kittur S, Hersh JH, Hornstein L (1985): Metacarpophalangeal pattern profile analysis in Sotos syndrome. Am J Med Genet 20:625-629.
-
(1985)
Am J Med Genet
, vol.20
, pp. 625-629
-
-
Butler, M.G.1
Meany, F.J.2
Kittur, S.3
Hersh, J.H.4
Hornstein, L.5
-
12
-
-
0024585418
-
A comprehensive and critical assessment of overgrowth and overgrowth syndromes
-
Cohen MM Jr (1989): A comprehensive and critical assessment of overgrowth and overgrowth syndromes. Adv Hum Genet 18:181-303.
-
(1989)
Adv Hum Genet
, vol.18
, pp. 181-303
-
-
Cohen Jr., M.M.1
-
13
-
-
0025078219
-
Syndrome of the Month: Sotos syndrome
-
Cole TRP, Hughes HE (1990): Syndrome of the Month: Sotos syndrome. J Med Genet 27:571-576.
-
(1990)
J Med Genet
, vol.27
, pp. 571-576
-
-
Cole, T.R.P.1
Hughes, H.E.2
-
14
-
-
0028078759
-
Sotos syndrome: A study of the diagnostic criteria and natural history
-
Cole TRP, Hughes HE (1994): Sotos syndrome: A study of the diagnostic criteria and natural history. J Med Genet 31:20-32.
-
(1994)
J Med Genet
, vol.31
, pp. 20-32
-
-
Cole, T.R.P.1
Hughes, H.E.2
-
16
-
-
0026598107
-
Small cell lung carcinoma in a patient with Sotos syndrome: Are genes at 3p21 involved in both conditions?
-
Cole TRP, Hughes HE, Jeffreys MJ, Williams GT, Arnold MM (1992): Small cell lung carcinoma in a patient with Sotos syndrome: Are genes at 3p21 involved in both conditions? J Med Genet 29:338-341.
-
(1992)
J Med Genet
, vol.29
, pp. 338-341
-
-
Cole, T.R.P.1
Hughes, H.E.2
Jeffreys, M.J.3
Williams, G.T.4
Arnold, M.M.5
-
17
-
-
0022429363
-
Weaver's syndrome - Primordial excessive growth velocity: A case report
-
Dawood AA, Machado GT, Winship WS (1985): Weaver's syndrome - primordial excessive growth velocity: A case report. S Afr Med J 67: 646-648.
-
(1985)
S Afr Med J
, vol.67
, pp. 646-648
-
-
Dawood, A.A.1
Machado, G.T.2
Winship, W.S.3
-
18
-
-
0032476003
-
Inherited macrocephaly-hamartoma syndromes
-
DiLiberti JH (1998): Inherited macrocephaly-hamartoma syndromes. Am J Med Genet 79:284-290.
-
(1998)
Am J Med Genet
, vol.79
, pp. 284-290
-
-
DiLiberti, J.H.1
-
20
-
-
0027742976
-
Twins and their mildly affected mother with Weaver syndrome
-
Dumić M, Vuković J, Cvitković M, Medica I (1993): Twins and their mildly affected mother with Weaver syndrome. Clin Genet 44:338-340.
-
(1993)
Clin Genet
, vol.44
, pp. 338-340
-
-
Dumić, M.1
Vuković, J.2
Cvitković, M.3
Medica, I.4
-
21
-
-
0032567994
-
Nevo syndrome
-
Dumić M, Vukelić D, Plavšić V, Cviko A, Sokolić L, Filipović-Grčić (1998): Nevo syndrome. Am J Med Genet 76:67-70.
-
(1998)
Am J Med Genet
, vol.76
, pp. 67-70
-
-
Dumić, M.1
Vukelić, D.2
Plavšić, V.3
Cviko, A.4
Sokolić, L.5
Filipović-Grčić6
-
22
-
-
0021929313
-
Brief clinical report: Weaver syndrome with pes cavus
-
Farrell SA, Hughes HE (1985): Brief clinical report: Weaver syndrome with pes cavus. Am J Med Genet 21:737-739.
-
(1985)
Am J Med Genet
, vol.21
, pp. 737-739
-
-
Farrell, S.A.1
Hughes, H.E.2
-
23
-
-
0022036584
-
Update on the Marshall-Smith-Weaver controversy
-
Fitch N (1985): Update on the Marshall-Smith-Weaver controversy (letter). Am J Med Genet 20:559-562.
-
(1985)
Am J Med Genet
, vol.20
, pp. 559-562
-
-
Fitch, N.1
-
24
-
-
0024204732
-
Retarded skeletal maturation in Weaver syndrome
-
Fretzayas A, Papanicolaou A, Tzanetakos K, Theodoridis C, Karpathios T (1988): Retarded skeletal maturation in Weaver syndrome. Acta Paediatr Scand 77:930-932.
-
(1988)
Acta Paediatr Scand
, vol.77
, pp. 930-932
-
-
Fretzayas, A.1
Papanicolaou, A.2
Tzanetakos, K.3
Theodoridis, C.4
Karpathios, T.5
-
25
-
-
0030949105
-
Autosomal dominant inheritance of the Weaver syndrome
-
Fryer A, Smith C, Rosenbloom L, Cole T (1997): Autosomal dominant inheritance of the Weaver syndrome. J Med Genet 34:418-419.
-
(1997)
J Med Genet
, vol.34
, pp. 418-419
-
-
Fryer, A.1
Smith, C.2
Rosenbloom, L.3
Cole, T.4
-
28
-
-
0024364928
-
Brief clinical report: Weaver syndrome: The changing phenotype in an adult
-
Greenberg F, Wasiewski W, McCabe ERB (1989): Brief clinical report: Weaver syndrome: The changing phenotype in an adult. Am J Med Genet 33:127-129.
-
(1989)
Am J Med Genet
, vol.33
, pp. 127-129
-
-
Greenberg, F.1
Wasiewski, W.2
McCabe, E.R.B.3
-
29
-
-
0019940363
-
Male to male transmission of cerebral gigantism
-
Halal F (1982): Male to male transmission of cerebral gigantism. Am J Med Genet 12:411-419.
-
(1982)
Am J Med Genet
, vol.12
, pp. 411-419
-
-
Halal, F.1
-
30
-
-
0020760607
-
Letter to the editor: Cerebral gigantism, intestinal polyposis, and pigmentary spotting of the genitalia
-
Halal F (1983): Letter to the editor: Cerebral gigantism, intestinal polyposis, and pigmentary spotting of the genitalia. Am J Med Genet 15:161.
-
(1983)
Am J Med Genet
, vol.15
, pp. 161
-
-
Halal, F.1
-
31
-
-
0022293660
-
Weaver syndrome: Expanded natural history
-
Hall BD (1985): Weaver syndrome: Expanded natural history. Prog Clin Biol Res 200:123-144.
-
(1985)
Prog Clin Biol Res
, vol.200
, pp. 123-144
-
-
Hall, B.D.1
-
32
-
-
0017287698
-
Familial occurrence of cerebral gigantism, Sotos' syndrome
-
Hansen FJ, Friis B (1976): Familial occurrence of cerebral gigantism, Sotos' syndrome. Acta Paediatr Scand 65:387-389.
-
(1976)
Acta Paediatr Scand
, vol.65
, pp. 387-389
-
-
Hansen, F.J.1
Friis, B.2
-
34
-
-
0014095257
-
Cerebral gigantism: Endocrinological and clinical observations of six patients including a congenital giant, concordant monozygotic twins, and a child who achieved adult gigantic size
-
Hook EB, Reynolds JW (1967): Cerebral gigantism: Endocrinological and clinical observations of six patients including a congenital giant, concordant monozygotic twins, and a child who achieved adult gigantic size. J Pediatr 70:900-914.
-
(1967)
J Pediatr
, vol.70
, pp. 900-914
-
-
Hook, E.B.1
Reynolds, J.W.2
-
36
-
-
0020954266
-
Advance de la maturation osseuse et syndrome dysmorphique chez deux germains (syndrome de Marshall-Weaver)
-
Jalaguier J, Montoya F, Germain M, Bonnet H (1983): Advance de la maturation osseuse et syndrome dysmorphique chez deux germains (syndrome de Marshall-Weaver). J Genet Hum 31:385-395.
-
(1983)
J Genet Hum
, vol.31
, pp. 385-395
-
-
Jalaguier, J.1
Montoya, F.2
Germain, M.3
Bonnet, H.4
-
37
-
-
0004523640
-
The Golabi-Rosen syndrome
-
Letter to the editor
-
Kajii T, Tsukahara M (1984): The Golabi-Rosen syndrome. Letter to the editor. Am J Med Genet 19:819.
-
(1984)
Am J Med Genet
, vol.19
, pp. 819
-
-
Kajii, T.1
Tsukahara, M.2
-
38
-
-
0023131691
-
Congenital heart defects in Sotos sequence
-
Kaneko H, Tsukahara M, Tachibana H, Kurashige H, Kuwano A, Kajii T (1987): Congenital heart defects in Sotos sequence. Am J Med Genet 26:569-576.
-
(1987)
Am J Med Genet
, vol.26
, pp. 569-576
-
-
Kaneko, H.1
Tsukahara, M.2
Tachibana, H.3
Kurashige, H.4
Kuwano, A.5
Kajii, T.6
-
39
-
-
0005666060
-
Weaver-like syndrome with hyperprogesteronemia and maternal luteoma
-
Kelly T, Stelling M, Wilson T (1983): Weaver-like syndrome with hyperprogesteronemia and maternal luteoma. Proc Greenwood Genet Ctr 2:128-129.
-
(1983)
Proc Greenwood Genet Ctr
, vol.2
, pp. 128-129
-
-
Kelly, T.1
Stelling, M.2
Wilson, T.3
-
40
-
-
0025010176
-
A Japanese male infant with the Weaver syndrome
-
Kondo I, Mori Y, Kuwajima K (1990): A Japanese male infant with the Weaver syndrome. J Hum Genet 35:257-262.
-
(1990)
J Hum Genet
, vol.35
, pp. 257-262
-
-
Kondo, I.1
Mori, Y.2
Kuwajima, K.3
-
41
-
-
0026005281
-
Weaver syndrome in two Japanese children
-
Kondo I, Mori Y, Kuwajima K (1991): Weaver syndrome in two Japanese children. Am J Med Genet 41:221-224.
-
(1991)
Am J Med Genet
, vol.41
, pp. 221-224
-
-
Kondo, I.1
Mori, Y.2
Kuwajima, K.3
-
43
-
-
0028297939
-
Child with Sotos phenotype and a 5:15 translocation
-
Maroun C, Schmerler S, Hutcheon RG (1994): Child with Sotos phenotype and a 5:15 translocation. Am J Med Genet 50:291-293.
-
(1994)
Am J Med Genet
, vol.50
, pp. 291-293
-
-
Maroun, C.1
Schmerler, S.2
Hutcheon, R.G.3
-
44
-
-
0031203265
-
Germline mutations in PTEN are present in Bannayan-Zonana syndrome
-
Marsh DJ, Dahia PLM, Zheng Z, Liaw D, Parsons R, Gorlin RJ, Eng C (1997): Germline mutations in PTEN are present in Bannayan-Zonana syndrome. Nat Genet 16:333-334.
-
(1997)
Nat Genet
, vol.16
, pp. 333-334
-
-
Marsh, D.J.1
Dahia, P.L.M.2
Zheng, Z.3
Liaw, D.4
Parsons, R.5
Gorlin, R.J.6
Eng, C.7
-
49
-
-
0025283930
-
Weaver syndrome and instability of the upper cervical spine
-
Muhonen MG, Menezes AH (1990): Weaver syndrome and instability of the upper cervical spine. J Pediatr 116:596-599.
-
(1990)
J Pediatr
, vol.116
, pp. 596-599
-
-
Muhonen, M.G.1
Menezes, A.H.2
-
51
-
-
0016249746
-
Evidence for autosomal recessive inheritance in cerebral gigantism
-
Nevo S, Zeltzer M, Benderly A, Levy J (1974): Evidence for autosomal recessive inheritance in cerebral gigantism. J Med Genet 11:158-165.
-
(1974)
J Med Genet
, vol.11
, pp. 158-165
-
-
Nevo, S.1
Zeltzer, M.2
Benderly, A.3
Levy, J.4
-
52
-
-
0030604922
-
Propositus with Weaver syndrome and his mildly-affected mother: Implication of nontraditional inheritance
-
Nishimura G, Hasegawa T, Nagai T (1996): Propositus with Weaver syndrome and his mildly-affected mother: Implication of nontraditional inheritance. Am J Med Genet 65:249-251.
-
(1996)
Am J Med Genet
, vol.65
, pp. 249-251
-
-
Nishimura, G.1
Hasegawa, T.2
Nagai, T.3
-
54
-
-
0025746685
-
Weaver syndrome: A case without early overgrowth and review of the literature
-
Ramos-Arroyo MA, Weaver DD, Banks ER (1991): Weaver syndrome: A case without early overgrowth and review of the literature. Pediatrics 88:1106-1111.
-
(1991)
Pediatrics
, vol.88
, pp. 1106-1111
-
-
Ramos-Arroyo, M.A.1
Weaver, D.D.2
Banks, E.R.3
-
55
-
-
0025909896
-
A sporadic case of Weaver syndrome in a female
-
Rojas-Martínez A, Sánchez-Corona J, García-Cruz MO, Gonzáles-Martínez A, Nazará Z, García-Cruz D (1991): A sporadic case of Weaver syndrome in a female. Dysmorphol Clin Genet 5:23-26.
-
(1991)
Dysmorphol Clin Genet
, vol.5
, pp. 23-26
-
-
Rojas-Martínez, A.1
Sánchez-Corona, J.2
García-Cruz, M.O.3
Gonzáles-Martínez, A.4
Nazará, Z.5
García-Cruz, D.6
-
56
-
-
0020626312
-
Siblings with the Weaver syndrome
-
Roussounis S, Crawford M (1983): Siblings with the Weaver syndrome. J Pediatr 10:595-597.
-
(1983)
J Pediatr
, vol.10
, pp. 595-597
-
-
Roussounis, S.1
Crawford, M.2
-
57
-
-
0019195703
-
Sotos syndrome with intestinal polyposis and pigmentary spotting of the genitalia
-
Ruvalcaba RHA, Myhre S, Smith DW (1980): Sotos syndrome with intestinal polyposis and pigmentary spotting of the genitalia. Clin Genet 18:413-416.
-
(1980)
Clin Genet
, vol.18
, pp. 413-416
-
-
Ruvalcaba, R.H.A.1
Myhre, S.2
Smith, D.W.3
-
59
-
-
0343435169
-
Gigantism (acromegalic in type)
-
Schlesinger B (1931): Gigantism (acromegalic in type). Proc R Soc Med 24:1352.
-
(1931)
Proc R Soc Med
, vol.24
, pp. 1352
-
-
Schlesinger, B.1
-
60
-
-
0025272183
-
Sotos syndrome and de novo balanced autosomal translocation [t(3;6)(p21;p21)]
-
Schrander-Stumpel CT, Fryns JP, Hamers GG (1990): Sotos syndrome and de novo balanced autosomal translocation [t(3;6)(p21;p21)]. Clin Genet 37:226-229.
-
(1990)
Clin Genet
, vol.37
, pp. 226-229
-
-
Schrander-Stumpel, C.T.1
Fryns, J.P.2
Hamers, G.G.3
-
62
-
-
0031020714
-
No evidence for uniparental disomy as a common cause of Sotos syndrome
-
Smith M, Fullwood P, Qi Y, Palmer S, Upadhyaya M, Cole T (1997): No evidence for uniparental disomy as a common cause of Sotos syndrome. J Med Genet 34:10-12.
-
(1997)
J Med Genet
, vol.34
, pp. 10-12
-
-
Smith, M.1
Fullwood, P.2
Qi, Y.3
Palmer, S.4
Upadhyaya, M.5
Cole, T.6
-
63
-
-
0001445647
-
Cerebral gigantism in childhood: A syndrome of excessively rapid growth with acromelic features and a non-progressive neurologic disorder
-
Sotos JF, Dodge PR, Muirhead D, Crawford JD, Talbot NB (1964): Cerebral gigantism in childhood: A syndrome of excessively rapid growth with acromelic features and a non-progressive neurologic disorder. N Engl J Med 271:109-116.
-
(1964)
N Engl J Med
, vol.271
, pp. 109-116
-
-
Sotos, J.F.1
Dodge, P.R.2
Muirhead, D.3
Crawford, J.D.4
Talbot, N.B.5
-
65
-
-
0022352487
-
A Weaver-like syndrome with endocrinological abnormalities in a boy and his mother
-
Stoll C, Talon P, Mengus L, Roth MP, Dott B (1985): A Weaver-like syndrome with endocrinological abnormalities in a boy and his mother. Clin Genet 28:255-259.
-
(1985)
Clin Genet
, vol.28
, pp. 255-259
-
-
Stoll, C.1
Talon, P.2
Mengus, L.3
Roth, M.P.4
Dott, B.5
-
66
-
-
0024407543
-
A new autosomal recessive disorder resembling Weaver syndrome
-
Teebi AS, Sundaresham TS, Hammouri MY, Al-Awadi SA, Al-Saleh QA (1989): A new autosomal recessive disorder resembling Weaver syndrome. Am J Med Genet 33:479-482.
-
(1989)
Am J Med Genet
, vol.33
, pp. 479-482
-
-
Teebi, A.S.1
Sundaresham, T.S.2
Hammouri, M.Y.3
Al-Awadi, S.A.4
Al-Saleh, Q.A.5
-
68
-
-
0025281669
-
Le syndrome de Weaver: A propos d'un nouveau cas
-
Paris
-
Trabelsi M, Ben Hariz MB, Monastiri K, Taktak M, Bennaceur B (1990): Le syndrome de Weaver: A propos d'un nouveau cas. Ann Pédiatr (Paris) 37:327-330.
-
(1990)
Ann Pédiatr
, vol.37
, pp. 327-330
-
-
Trabelsi, M.1
Ben Hariz, M.B.2
Monastiri, K.3
Taktak, M.4
Bennaceur, B.5
-
69
-
-
0021366645
-
A Weaver-like syndrome in a Japanese boy
-
Tsukahara M, Tanaka S, Kajii T (1984): A Weaver-like syndrome in a Japanese boy. Clin Genet 25:73-78.
-
(1984)
Clin Genet
, vol.25
, pp. 73-78
-
-
Tsukahara, M.1
Tanaka, S.2
Kajii, T.3
-
70
-
-
0022354902
-
Anesthetic problems associated with Weaver's syndrome
-
Turner DR, Downing JW (1985): Anesthetic problems associated with Weaver's syndrome. Br J Anaesth 57:1260-1263.
-
(1985)
Br J Anaesth
, vol.57
, pp. 1260-1263
-
-
Turner, D.R.1
Downing, J.W.2
-
71
-
-
0026410576
-
Chromosome aberrations in Sotos syndrome
-
Wajntal A, Koiffman CP (1991): Chromosome aberrations in Sotos syndrome (letter, comment). Clin Genet 40:472.
-
(1991)
Clin Genet
, vol.40
, pp. 472
-
-
Wajntal, A.1
Koiffman, C.P.2
-
72
-
-
0015989659
-
A new overgrowth syndrome with accelerated skeletal maturation, unusual facies, and camptodactyly
-
Weaver DD, Graham CB, Thomas IT, Smith DW (1974): A new overgrowth syndrome with accelerated skeletal maturation, unusual facies, and camptodactyly. J Pediatr 84:547-552.
-
(1974)
J Pediatr
, vol.84
, pp. 547-552
-
-
Weaver, D.D.1
Graham, C.B.2
Thomas, I.T.3
Smith, D.W.4
-
73
-
-
0019859358
-
Accelerated bone maturation syndrome of the Weaver type
-
Weisswichert PH, Knapp G, Willich E (1981): Accelerated bone maturation syndrome of the Weaver type. Eur J Pediatr 137:329-333.
-
(1981)
Eur J Pediatr
, vol.137
, pp. 329-333
-
-
Weisswichert, P.H.1
Knapp, G.2
Willich, E.3
-
75
-
-
0022379861
-
Sotos syndrome - Autosomal dominant inheritance substantiated
-
Winship IM (1985): Sotos syndrome - autosomal dominant inheritance substantiated. Clin Genet 28:243-246.
-
(1985)
Clin Genet
, vol.28
, pp. 243-246
-
-
Winship, I.M.1
-
76
-
-
0017200452
-
Cerebral gigantism - Apparent dominant inheritance
-
Zonana J, Rimoin DL, Fisher DA (1976): Cerebral gigantism - apparent dominant inheritance. Birth Defects 12(6):63-69.
-
(1976)
Birth Defects
, vol.12
, Issue.6
, pp. 63-69
-
-
Zonana, J.1
Rimoin, D.L.2
Fisher, D.A.3
-
77
-
-
0017410188
-
Dominant inheritance of cerebral gigantism
-
Zonana J, Sotos JF, Romshe CA, Fischer DA, Elders MJ, Rimoin DL (1977): Dominant inheritance of cerebral gigantism. J Pediatr 91:251-256.
-
(1977)
J Pediatr
, vol.91
, pp. 251-256
-
-
Zonana, J.1
Sotos, J.F.2
Romshe, C.A.3
Fischer, D.A.4
Elders, M.J.5
Rimoin, D.L.6
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