-
1
-
-
0025129182
-
Bannayan-Riley-Ruvaicaba syndrome: Renaming three formerly recognized syndromes as one etiologic entity
-
Cohen MM Jr. Bannayan-Riley-Ruvaicaba syndrome: renaming three formerly recognized syndromes as one etiologic entity. Am J Med Genet. 1990;35:291.
-
(1990)
Am J Med Genet
, vol.35
, pp. 291
-
-
Cohen Jr., M.M.1
-
2
-
-
0344410719
-
Bannayan-Riley-Ruvalcaba syndrome (Bannayan-Zonana syndrome, Ruvalcaba-Myhre, Riley-Smith syndrome)
-
Gorlin RS, Cohen MM, Leven LS, eds. New York, NY: Oxford University Press
-
Gorlin RS, Cohen MM, Leven LS. Bannayan-Riley-Ruvalcaba syndrome (Bannayan-Zonana syndrome, Ruvalcaba-Myhre, Riley-Smith syndrome). In: Gorlin RS, Cohen MM, Leven LS, eds. Syndromes of the Head and Neck. New York, NY: Oxford University Press; 1990:336-338.
-
(1990)
Syndromes of the Head and Neck
, pp. 336-338
-
-
Gorlin, R.S.1
Cohen, M.M.2
Leven, L.S.3
-
3
-
-
0020053384
-
The Bannavan syndrome: An autosomal dominant disorder consisting of macrocephaly, lipomas, hemangiomas, and risk for intracranial tumors
-
Higginbottom MC, Schultz P. The Bannavan syndrome: an autosomal dominant disorder consisting of macrocephaly, lipomas, hemangiomas, and risk for intracranial tumors. Pediatrics. 1982:69:632-634.
-
(1982)
Pediatrics
, vol.69
, pp. 632-634
-
-
Higginbottom, M.C.1
Schultz, P.2
-
4
-
-
0021676078
-
Macrocephaly with hamartomas: Bannayan-Zonana syndrome
-
Miles JH, Zonana J, McFarlane J, Aleck KA, Bawle E. Macrocephaly with hamartomas: Bannayan-Zonana syndrome. Am J Med Genet. 1984;19:225-234.
-
(1984)
Am J Med Genet
, vol.19
, pp. 225-234
-
-
Miles, J.H.1
Zonana, J.2
McFarlane, J.3
Aleck, K.A.4
Bawle, E.5
-
5
-
-
0024817610
-
Macrocephaly, multiple lipomas, and hemangiomata (Bannayan-Zonana syndrome): Genetic heterogeneity or autosomal dominant locus with at least two different allelic forms?
-
Moretti-Ferreira D, Koiffmann CP, Souza DH, Diament AJ, Wajntal A. Macrocephaly, multiple lipomas, and hemangiomata (Bannayan-Zonana syndrome): genetic heterogeneity or autosomal dominant locus with at least two different allelic forms? Am J Med Genet. 1989;34:548-551.
-
(1989)
Am J Med Genet
, vol.34
, pp. 548-551
-
-
Moretti-Ferreira, D.1
Koiffmann, C.P.2
Souza, D.H.3
Diament, A.J.4
Wajntal, A.5
-
6
-
-
0019940363
-
Male to male transmission of cerebral gigantism
-
Halal F. Male to male transmission of cerebral gigantism. Am J Med Genet. 1982;12:411-419.
-
(1982)
Am J Med Genet
, vol.12
, pp. 411-419
-
-
Halal, F.1
-
7
-
-
0020595287
-
Ruvalcaba-Myhre-Smith syndrome: A case with probable autosomal-dominant inheritance and additional manifestations
-
DiLiberti JH, Weleber RG, Budden S. Ruvalcaba-Myhre-Smith syndrome: a case with probable autosomal-dominant inheritance and additional manifestations. Am J Med Genet. 1983;15:491-495.
-
(1983)
Am J Med Genet
, vol.15
, pp. 491-495
-
-
Diliberti, J.H.1
Weleber, R.G.2
Budden, S.3
-
11
-
-
0025609195
-
Increased epidermal growth factor receptors in seborrheic keratoses and acrochordons of patients with the dysplastic nevus syndrome
-
Ellis DL, Nanney LB, King LE. Increased epidermal growth factor receptors in seborrheic keratoses and acrochordons of patients with the dysplastic nevus syndrome. J Am Acad Dermatol. 1990;23:1070-1077.
-
(1990)
J Am Acad Dermatol
, vol.23
, pp. 1070-1077
-
-
Ellis, D.L.1
Nanney, L.B.2
King, L.E.3
-
12
-
-
0001484667
-
Macrocephaly, pseudopapilledema and multiple hemangiomata: A previously undescribed heredofamilial syndrome
-
Riley HD, Smith WR. Macrocephaly, pseudopapilledema and multiple hemangiomata: a previously undescribed heredofamilial syndrome. Pediatrics. 1960; 26:293-300.
-
(1960)
Pediatrics
, vol.26
, pp. 293-300
-
-
Riley, H.D.1
Smith, W.R.2
-
13
-
-
0015094329
-
Lipomatosis, angiomatosis, and macrencephalia
-
Bannayan GA. Lipomatosis, angiomatosis, and macrencephalia. Arch Pathol. 1971;92:1-5.
-
(1971)
Arch Pathol
, vol.92
, pp. 1-5
-
-
Bannayan, G.A.1
-
14
-
-
0017186974
-
Macrocephaly with multiple lipomas and hemangiomas
-
Zonana J, Rimoin DL, Davis DC. Macrocephaly with multiple lipomas and hemangiomas. J Pediatr. 1976;89:600-603.
-
(1976)
J Pediatr
, vol.89
, pp. 600-603
-
-
Zonana, J.1
Rimoin, D.L.2
Davis, D.C.3
-
15
-
-
0019195703
-
Sotos syndrome with intestinal polyposis and pigmentary changes of the genitalia
-
Ruvalcaba RHA, Myhre S, Smith DW. Sotos syndrome with intestinal polyposis and pigmentary changes of the genitalia. Clin Genet. 1980;18:413-416.
-
(1980)
Clin Genet
, vol.18
, pp. 413-416
-
-
Ruvalcaba, R.H.A.1
Myhre, S.2
Smith, D.W.3
-
16
-
-
0020760607
-
Cerebral gigantism, intestinal poiyposis, and pigmentary spotting of the genitalia
-
Halal F. Cerebral gigantism, intestinal poiyposis, and pigmentary spotting of the genitalia. Am J Med Genet. 1983;15:161.
-
(1983)
Am J Med Genet
, vol.15
, pp. 161
-
-
Halal, F.1
-
17
-
-
4243543829
-
The large-for-gestational-age (LGA) infant in dysmorphic perspective
-
Willey AM, Carter TP, Kelly S, Porter IH, eds. New York, NY: Academic Press
-
Cohen MM Jr. The large-for-gestational-age (LGA) infant in dysmorphic perspective. In: Willey AM, Carter TP, Kelly S, Porter IH, eds. Clinical Genetics: Problems in Diagnosis and Counseling. New York, NY: Academic Press; 1982: 153-169.
-
(1982)
Clinical Genetics: Problems in Diagnosis and Counseling
, pp. 153-169
-
-
Cohen Jr., M.M.1
-
18
-
-
0023905733
-
Heredofamilial syndrome of mesodermal hamartomas, macrocephaly, and pseudopapilledema
-
Dvir M, Beer S, Aladjem M. Heredofamilial syndrome of mesodermal hamartomas, macrocephaly, and pseudopapilledema. Pediatrics. 1988;81:287-290.
-
(1988)
Pediatrics
, vol.81
, pp. 287-290
-
-
Dvir, M.1
Beer, S.2
Aladjem, M.3
-
19
-
-
0022649866
-
The Cowden syndrome: A clinical and genetic study in 21 patients
-
Starink TM, Van Der Veen JPW, Arwert F, et al. The Cowden syndrome: a clinical and genetic study in 21 patients. Clin Genet. 1986;29:222-233.
-
(1986)
Clin Genet
, vol.29
, pp. 222-233
-
-
Starink, T.M.1
Van Der Veen, J.P.W.2
Arwert, F.3
-
20
-
-
0021688438
-
Cowden's disease: Analysis of fourteen new cases
-
Starink TM. Cowden's disease: analysis of fourteen new cases. J Am Acad Dermatol. 1984;11:1127-1141.
-
(1984)
J Am Acad Dermatol
, vol.11
, pp. 1127-1141
-
-
Starink, T.M.1
|