-
1
-
-
0017900204
-
Recessively inherited costovertebral segmentation defect with mesomelia and peculiar facies (Covesdem syndrome) - A new genetic entity?
-
Wadia RS: Recessively inherited costovertebral segmentation defect with mesomelia and peculiar facies (Covesdem syndrome) - A new genetic entity? J Med Genet 15:123-127, 1978
-
(1978)
J Med Genet
, vol.15
, pp. 123-127
-
-
Wadia, R.S.1
-
2
-
-
18544403929
-
Covesdem syndrome
-
letter
-
Wadia RS: Covesdem syndrome. J Med Genet 16:162, 1979 (letter)
-
(1979)
J Med Genet
, vol.16
, pp. 162
-
-
Wadia, R.S.1
-
3
-
-
0015653167
-
Mesomelic dwarfism with hemivertebrae and small genetalia (the Robinow syndrome)
-
Wadlington WB, Tucker VL, Schimke RN: Mesomelic dwarfism with hemivertebrae and small genetalia (the Robinow syndrome). Am J Dis Child 126:202-205, 1973
-
(1973)
Am J Dis Child
, vol.126
, pp. 202-205
-
-
Wadlington, W.B.1
Tucker, V.L.2
Schimke, R.N.3
-
4
-
-
13144252787
-
Robinow syndrome, recessive form (costovertebral segmentation defect with mesomelia, included; Covesdem syndrome, included)
-
Baltimore, MD, John Hopkins University Press
-
McKusick VA, Francomano CA, Antonarakis SE (eds): Robinow syndrome, recessive form (costovertebral segmentation defect with mesomelia, included; Covesdem syndrome, included), in Mendelian Inheritance in Man (ed 10). Baltimore, MD, John Hopkins University Press, 1992, p 1685
-
(1992)
Mendelian Inheritance in Man (Ed 10)
, pp. 1685
-
-
McKusick, V.A.1
Francomano, C.A.2
Antonarakis, S.E.3
-
5
-
-
0022443827
-
Robinow syndrome without mesomelic brachymelia: A report of five cases
-
Bain MD, Winter RM, Burn J: Robinow syndrome without mesomelic brachymelia: A report of five cases. J Med Genet 23:350-354, 1986
-
(1986)
J Med Genet
, vol.23
, pp. 350-354
-
-
Bain, M.D.1
Winter, R.M.2
Burn, J.3
-
6
-
-
0024594994
-
Robinow syndrome with parental consanguinity
-
Glaser D, Herbst J, Roggenkamp K, et al: Robinow syndrome with parental consanguinity. Eur J Pediatr 148:652-653, 1989
-
(1989)
Eur J Pediatr
, vol.148
, pp. 652-653
-
-
Glaser, D.1
Herbst, J.2
Roggenkamp, K.3
-
7
-
-
0025159356
-
Autosomal recessive Robinow syndrome
-
Teebi AS: Autosomal recessive Robinow syndrome. Am J Med Genet 35:64-68, 1990
-
(1990)
Am J Med Genet
, vol.35
, pp. 64-68
-
-
Teebi, A.S.1
-
8
-
-
0025165804
-
Concurrence of Robinow syndrome and Crigler-Najar syndrome in two offspring of first cousins
-
Nazer H, Gunasekaran TS, Nyhan WL: Concurrence of Robinow syndrome and Crigler-Najar syndrome in two offspring of first cousins. Am J Med Genet 37:516-518, 1990
-
(1990)
Am J Med Genet
, vol.37
, pp. 516-518
-
-
Nazer, H.1
Gunasekaran, T.S.2
Nyhan, W.L.3
-
9
-
-
0015652687
-
Robinow dwarfism syndrome accompanied by penile agenesis and hemivertebrae
-
Vera-Roman JM: Robinow dwarfism syndrome accompanied by penile agenesis and hemivertebrae. Am J Dis Child 126:206-208, 1973
-
(1973)
Am J Dis Child
, vol.126
, pp. 206-208
-
-
Vera-Roman, J.M.1
-
10
-
-
0020039280
-
Robinow's syndrome: Partial primary hypogonadism in pubertal boys, with persistence of micropenis
-
Lee PA, Migeon CJ, Brown TR, et al: Robinow's syndrome: Partial primary hypogonadism in pubertal boys, with persistence of micropenis. Am J Dis Child 136:327-330, 1982
-
(1982)
Am J Dis Child
, vol.136
, pp. 327-330
-
-
Lee, P.A.1
Migeon, C.J.2
Brown, T.R.3
-
11
-
-
0027202255
-
The Robinow (fetal face) syndrome: A continuing puzzle
-
Robinow M: The Robinow (fetal face) syndrome: A continuing puzzle. Clin Dysmorphol 2:189-198, 1993
-
(1993)
Clin Dysmorphol
, vol.2
, pp. 189-198
-
-
Robinow, M.1
-
12
-
-
0017261757
-
Longitudinal standards for height, weight, height velocity, weight velocity and stages of puberty
-
Tanner JM, Whitehouse RH: Longitudinal standards for height, weight, height velocity, weight velocity and stages of puberty. Arch Dis Child 51:170-179, 1976
-
(1976)
Arch Dis Child
, vol.51
, pp. 170-179
-
-
Tanner, J.M.1
Whitehouse, R.H.2
-
14
-
-
0003556467
-
-
Palo Alto, CA, Stanford University Press
-
Greulich WW, Pyle SI: Radiographic Atlas of Skeletal Development of Hands and Wrist. Palo Alto, CA, Stanford University Press, 1959, pp 65-112
-
(1959)
Radiographic Atlas of Skeletal Development of Hands and Wrist
, pp. 65-112
-
-
Greulich, W.W.1
Pyle, S.I.2
-
15
-
-
0009079514
-
Assessment of endocrine functions
-
Baltimore, MD, Williams & Wilkins
-
Bertrand J, Rappaport R, Sizonenko PC (eds): Assessment of endocrine functions, in Pediatric Endocrinology, Physiology, Pathophysiology, and Clinical Aspects. Baltimore, MD, Williams & Wilkins, 1993, pp 658-681
-
(1993)
Pediatric Endocrinology, Physiology, Pathophysiology, and Clinical Aspects
, pp. 658-681
-
-
Bertrand, J.1
Rappaport, R.2
Sizonenko, P.C.3
-
17
-
-
13144259345
-
The relationship between growth velocity and growth hormone secretion in short prepubertal children
-
Oxf
-
Hindmarsh PC, Smith PJ, Brook CGD: The relationship between growth velocity and growth hormone secretion in short prepubertal children. Clin Endocrinol (Oxf) 1:154-158, 1987
-
(1987)
Clin Endocrinol
, vol.1
, pp. 154-158
-
-
Hindmarsh, P.C.1
Smith, P.J.2
Brook, C.G.D.3
-
18
-
-
0027202256
-
Congenital heart disease and Robinow syndrome
-
Atalay S, Ege B, Imamoglu A, et al: Congenital heart disease and Robinow syndrome. Clin Dysmorphol 2:208-210, 1993
-
(1993)
Clin Dysmorphol
, vol.2
, pp. 208-210
-
-
Atalay, S.1
Ege, B.2
Imamoglu, A.3
-
19
-
-
0025325217
-
Robinow syndrome: Report of two patients with cystic kidney disease
-
Wiens L, Strickland DK, Sniffen B, et al: Robinow syndrome: Report of two patients with cystic kidney disease. Clin Genet 37:481-484, 1990
-
(1990)
Clin Genet
, vol.37
, pp. 481-484
-
-
Wiens, L.1
Strickland, D.K.2
Sniffen, B.3
-
20
-
-
0026750158
-
Robinow syndrome in two siblings from consanguinous parents
-
Schorderet DF, Dahoun S, Defrance I, et al: Robinow syndrome in two siblings from consanguinous parents. Eur J Pediatr 151:586-589, 1992
-
(1992)
Eur J Pediatr
, vol.151
, pp. 586-589
-
-
Schorderet, D.F.1
Dahoun, S.2
Defrance, I.3
-
21
-
-
0025295274
-
Robinow or "fetal face" syndrome in a male with ambiguous genetalia and receptor deficiency
-
Schnau E, Pfeiffer RA, Schweikert HU, et al: Robinow or "fetal face" syndrome in a male with ambiguous genetalia and receptor deficiency. Eur J Pediatr 149:615-617, 1990
-
(1990)
Eur J Pediatr
, vol.149
, pp. 615-617
-
-
Schnau, E.1
Pfeiffer, R.A.2
Schweikert, H.U.3
-
22
-
-
0016582474
-
Fetal face syndrome (Robinow syndrome)
-
Gellis SS, Feingold M: Fetal face syndrome (Robinow syndrome). Am J Dis Child 129:351-352, 1975
-
(1975)
Am J Dis Child
, vol.129
, pp. 351-352
-
-
Gellis, S.S.1
Feingold, M.2
-
23
-
-
85030269772
-
Dynamic pituitary function and bone density measurement in normal size empty sella syndrome
-
The Endocrine Society, Las Vegas, NV, June 14-18, abstr 1613c
-
Michaels R, Robinson D, Sollock R, et al: Dynamic pituitary function and bone density measurement in normal size empty sella syndrome. Seventy-fifth Annual Meeting, The Endocrine Society, Las Vegas, NV, June 14-18, 1993 (abstr 1613c)
-
(1993)
Seventy-fifth Annual Meeting
-
-
Michaels, R.1
Robinson, D.2
Sollock, R.3
|