-
1
-
-
0014545047
-
Scalp defects in trisomy 13
-
Abuelo D, Feingold M (1969). Scalp defects in trisomy 13. Clin Pediatr 8:415-417.
-
(1969)
Clin Pediatr
, vol.8
, pp. 415-417
-
-
Abuelo, D.1
Feingold, M.2
-
2
-
-
0023806505
-
Clinical features in a de novo interstitial deletion 15q13 to q15
-
Autio S, Pihko H, Tengström C (1988). Clinical features in a de novo interstitial deletion 15q13 to q15. Clin Genet 34:293-298.
-
(1988)
Clin Genet
, vol.34
, pp. 293-298
-
-
Autio, S.1
Pihko, H.2
Tengström, C.3
-
3
-
-
0029040780
-
Aplasia cutis congenita and associated disorders: An update
-
Evers M, Steijlen P, Hamel B (1995). Aplasia cutis congenita and associated disorders: an update. Clin Genet 47:295-301.
-
(1995)
Clin Genet
, vol.47
, pp. 295-301
-
-
Evers, M.1
Steijlen, P.2
Hamel, B.3
-
4
-
-
0024207171
-
Interstitial deletion of chromosome 15: Two cases
-
Formiga L, Poenaru L, Couronne F, Flori E, Eibel J, Deminatti M, Savary J, Lai J, Gilgenkranz S, Pierson M (1988). Interstitial deletion of chromosome 15: two cases. Hunt Genet 80:401-404.
-
(1988)
Hunt Genet
, vol.80
, pp. 401-404
-
-
Formiga, L.1
Poenaru, L.2
Couronne, F.3
Flori, E.4
Eibel, J.5
Deminatti, M.6
Savary, J.7
Lai, J.8
Gilgenkranz, S.9
Pierson, M.10
-
5
-
-
0022655534
-
Aplasia cutis congenita: A clinical review and proposal for classification
-
Frieden IJ (1986). Aplasia cutis congenita: A clinical review and proposal for classification. J. Am Acad Dermatol 14:646-660.
-
(1986)
J. Am Acad Dermatol
, vol.14
, pp. 646-660
-
-
Frieden, I.J.1
-
6
-
-
0020043629
-
Interstitial deletion of the long arm of chromosome 15
-
Fryns J, Muelenaere A, van den Berghe H (1982). Interstitial deletion of the long arm of chromosome 15. Ann Genet 25:59-60.
-
(1982)
Ann Genet
, vol.25
, pp. 59-60
-
-
Fryns, J.1
Muelenaere, A.2
Van den Berghe, H.3
-
7
-
-
0025282844
-
Craniosynostosis in an infant with an interstitial deletion of 15q [46, XY, del (15)(q15q22.1)]
-
Fukushima Y, Wakui K, Nishida T, Nishimoto H (1990). Craniosynostosis in an infant with an interstitial deletion of 15q [46, XY, del (15)(q15q22.1)]. Am J Med Genet 36:209-213.
-
(1990)
Am J Med Genet
, vol.36
, pp. 209-213
-
-
Fukushima, Y.1
Wakui, K.2
Nishida, T.3
Nishimoto, H.4
-
8
-
-
0026033981
-
Interstitial 15q deletion without a classic Prader-Willi phenotype
-
Galan F, Aguillar M, Gonzalez J, Clemente F, Sanchez R, Tapia M, Moya M (1991). Interstitial 15q deletion without a classic Prader-Willi phenotype. Am J Med Genet 38:532-534.
-
(1991)
Am J Med Genet
, vol.38
, pp. 532-534
-
-
Galan, F.1
Aguillar, M.2
Gonzalez, J.3
Clemente, F.4
Sanchez, R.5
Tapia, M.6
Moya, M.7
-
9
-
-
0025047781
-
A de novo interstitial deletion of 15(q21.2q22.1) in a moderately retarded adult male
-
Martin F, Platt J, Tawn E, Burn J (1990). A de novo interstitial deletion of 15(q21.2q22.1) in a moderately retarded adult male. J Med Genet 27:637-639.
-
(1990)
J Med Genet
, vol.27
, pp. 637-639
-
-
Martin, F.1
Platt, J.2
Tawn, E.3
Burn, J.4
-
10
-
-
0023521838
-
Deletion 15q21.1-q22.1 resulting from a paternal insertion into chromosome 5
-
Yip MY, Selikowitz M, Don N Kovacic A, Purvis-Smith S, Lam-Po-Tang PRL (1987). Deletion 15q21.1-q22.1 resulting from a paternal insertion into chromosome 5. J Med Genet 24:709-712.
-
(1987)
J Med Genet
, vol.24
, pp. 709-712
-
-
Yip, M.Y.1
Selikowitz, M.2
Don, N.3
Kovacic, A.4
Purvis-Smith, S.5
Lam-Po-Tang, P.R.L.6
-
11
-
-
0018168775
-
The characterization of high-resolution G-banded chromosomes of man
-
Yunis JJ, Sawyer JR, Ball DW (1978). The characterization of high-resolution G-banded chromosomes of man. Chromosoma 67:293-307.
-
(1978)
Chromosoma
, vol.67
, pp. 293-307
-
-
Yunis, J.J.1
Sawyer, J.R.2
Ball, D.W.3
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