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1.

Polymorphisms associated with low bone mass and high risk of atraumatic fracture.

Zofkova, I; Nemcikova, P; Kuklik, M.

Physiol Res ; 64(5): 621-31, 2015.

Artigo em Inglês | MEDLINE | ID: mdl-25804099

2.

Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism.

Karadima, G; Bugge, M; Nicolaidis, P; Vassilopoulos, D; Avramopoulos, D; Grigoriadou, M; Albrecht, B; Passarge, E; Annerén, G; Blennow, E; Clausen, N; Galla-Voumvouraki, A; Tsezou, A; Kitsiou-Tzeli, S; Hahnemann, J M; Hertz, J M; Houge, G; Kuklík, M; Macek, M; Lacombe, D; Miller, K; Moncla, A; López Pajares, I; Patsalis, P C; Petersen, M B.

Eur J Hum Genet ; 6(5): 432-8, 1998.

Artigo em Inglês | MEDLINE | ID: mdl-9801867

3.

Poland-Möbius syndrome and disruption spectrum affecting the face and extremities: a review paper and presentation of five cases.

Kuklík, M.

Acta Chir Plast ; 42(3): 95-103, 2000.

Artigo em Inglês | MEDLINE | ID: mdl-11059047

4.

Precision grip with congenital hypoplasty or hypofunction of the thumb.

Smrcka, V; Dylevský, I; Kuklík, M.

Acta Chir Plast ; 41(4): 107-11, 1999.

Artigo em Inglês | MEDLINE | ID: mdl-10743713

5.

[Arthrogryposis multiplex congenita. I.]. / Arthrogryposis multiplex congenita.

Marík, I; Schejbalová, A; Kuklík, M; Kraus, J.

Acta Chir Orthop Traumatol Cech ; 59(1): 11-8, 1992.

Artigo em Tcheco | MEDLINE | ID: mdl-20429982

6.

[Flexional adduction contracture of the thumbs in distal arthrogryposis type I.]. / Flekcne addukcní kontraktura palcu rukou u distální artrogrypózy typu I.

Marík, I; Vrabec, R; Kuklík, M; Kraus, J.

Acta Chir Orthop Traumatol Cech ; 59(4): 246-52, 1992.

Artigo em Tcheco | MEDLINE | ID: mdl-20483094

7.

[Arthrogryposis Multiplex Congenita - Part II.]. / Arthrogryposis multiplex congenita (2. cást).

Marík, I; Kuklík, M; Kraus, J; Schejbalová, A; Kubát, R.

Acta Chir Orthop Traumatol Cech ; 59(2): 67-76, 1992.

Artigo em Tcheco | MEDLINE | ID: mdl-20483061

8.

[Dermatoglyphic characteristics of the Czech population]. / Dermatoglyfické charakteristiky ceské populace.

Kuklík, M.

Cas Lek Cesk ; 130(20-21): 606-9, 1991 Nov 18.

Artigo em Tcheco | MEDLINE | ID: mdl-1769057

9.

[Ectodermal dysplasia with alopecia, a higher rate of chromosome breaks and normal dentition]. / Ektodermální dysplázie s alopecií, vyssí frekvencí chromosomových zlomu a normální denticí.

Kuklík, M.

Cas Lek Cesk ; 129(40): 1266-70, 1990 Oct 05.

Artigo em Tcheco | MEDLINE | ID: mdl-2257571

10.

[The ADAM syndrome]. / Syndrom ADAM.

Kuklík, M.

Cas Lek Cesk ; 129(24): 757-60, 1990 Jun 15.

Artigo em Tcheco | MEDLINE | ID: mdl-2393884

11.

[Clinical and genetic characteristics of the Klippel-Trenaunay syndrome]. / Klinická a genetická charakteristika syndromu Klippel-Trenaunay.

Kuklík, M; Krejcík, J; Marík, J.

Cas Lek Cesk ; 129(36): 1133-7, 1990 Sep 07.

Artigo em Tcheco | MEDLINE | ID: mdl-2171774

12.

[Deviations in dermatoglyphic signs in juvenile hypertensives]. / Odchylky dermatoglyfických znaku u juvenilních hypertoniku.

Palyzová, D; Kuklík, M; Beránková, M; Karhan, T.

Cas Lek Cesk ; 129(14): 438-42, 1990 Apr 06.

Artigo em Tcheco | MEDLINE | ID: mdl-2344601

13.

[An unusual case of primary hyperparathyroidism in a woman with Gorlin-Goltz syndrome]. / Neobvyklý prípad primární hyperparatyreózy u nemocné se syndromem Gorlina-Goltze.

Zofková, I; Kuklík, M; Novák, Z; Betka, J; Dorazilová, V.

Vnitr Lek ; 46(6): 347-9, 2000 Jun.

Artigo em Tcheco | MEDLINE | ID: mdl-15645841

14.

[Osteogenesis imperfecta. I. Clinico-genetic characteristics]. / Osteogenesis imperfecta. I. Klinicko-genetická charakteristika.

Marík, I; Kuklík, M; Kubát, R.

Acta Chir Orthop Traumatol Cech ; 55(4): 318-26, 1988 Jul.

Artigo em Tcheco | MEDLINE | ID: mdl-3176797

15.

[Osteogenesis imperfecta. II. Differential diagnosis and therapy]. / Osteogenesis imperfecta. II. Diferenciální diagnostika a terapie.

Marík, I; Kuklík, M; Kubát, R.

Acta Chir Orthop Traumatol Cech ; 55(4): 327-34, 1988 Jul.

Artigo em Tcheco | MEDLINE | ID: mdl-3176798

16.

[Primary dysplastic ossification of the hip joints]. / Primární dysplastická osifikace kycelních kloubu.

Marík, I; Zeman, J; Kuklík, M.

Acta Chir Orthop Traumatol Cech ; 51(3): 241-7, 1984 Jun.

Artigo em Tcheco | MEDLINE | ID: mdl-6433608

17.

[The 48 XXYY syndrome]. / Syndrom 48, XXYY.

Kuklík, M; Handzel, J; Klán, Z.

Cas Lek Cesk ; 125(30): 944-6, 1986 Jul 25.

Artigo em Tcheco | MEDLINE | ID: mdl-3731234

18.

[Statistical study of quantitative dactyloscopy and dermatologic signs in families with Down's syndrome]. / Statistická studie kvantitativních daktyloskopických a dermatoglyfických znaku v rodinách s morbus Down.

Kuklík, M; Srajer, J; Padysák, P.

Cas Lek Cesk ; 125(4): 106-10, 1986 Jan 24.

Artigo em Tcheco | MEDLINE | ID: mdl-2936455

19.

[Dermatoglyphic findings in families with spontaneous abortions]. / Dermatoglyfické nálezy v rodinách se spontánními potraty.

Kuklík, M; Losan, F; Srajer, J; Maresová, H.

Cas Lek Cesk ; 125(8): 240-4, 1986 Feb 21.

Artigo em Tcheco | MEDLINE | ID: mdl-3955616

20.

[The mosaic form of Down's syndrome]. / Mozaiková forma Downova syndromu.

Losan, F; Maresová, H; Kuklík, M; Macek, M; Subrt, I.

Cas Lek Cesk ; 125(30): 933-6, 1986 Jul 25.

Artigo em Tcheco | MEDLINE | ID: mdl-2942258

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Polymorphisms associated with low bone mass and high risk of atraumatic fracture.

Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism.

Poland-Möbius syndrome and disruption spectrum affecting the face and extremities: a review paper and presentation of five cases.

Precision grip with congenital hypoplasty or hypofunction of the thumb.

[Arthrogryposis multiplex congenita. I.]. / Arthrogryposis multiplex congenita.

[Flexional adduction contracture of the thumbs in distal arthrogryposis type I.]. / Flekcne addukcní kontraktura palcu rukou u distální artrogrypózy typu I.

[Arthrogryposis Multiplex Congenita - Part II.]. / Arthrogryposis multiplex congenita (2. cást).

[Dermatoglyphic characteristics of the Czech population]. / Dermatoglyfické charakteristiky ceské populace.

[Ectodermal dysplasia with alopecia, a higher rate of chromosome breaks and normal dentition]. / Ektodermální dysplázie s alopecií, vyssí frekvencí chromosomových zlomu a normální denticí.

[The ADAM syndrome]. / Syndrom ADAM.

[Clinical and genetic characteristics of the Klippel-Trenaunay syndrome]. / Klinická a genetická charakteristika syndromu Klippel-Trenaunay.

[Deviations in dermatoglyphic signs in juvenile hypertensives]. / Odchylky dermatoglyfických znaku u juvenilních hypertoniku.

[An unusual case of primary hyperparathyroidism in a woman with Gorlin-Goltz syndrome]. / Neobvyklý prípad primární hyperparatyreózy u nemocné se syndromem Gorlina-Goltze.

[Osteogenesis imperfecta. I. Clinico-genetic characteristics]. / Osteogenesis imperfecta. I. Klinicko-genetická charakteristika.

[Osteogenesis imperfecta. II. Differential diagnosis and therapy]. / Osteogenesis imperfecta. II. Diferenciální diagnostika a terapie.

[Primary dysplastic ossification of the hip joints]. / Primární dysplastická osifikace kycelních kloubu.

[The 48 XXYY syndrome]. / Syndrom 48, XXYY.

[Statistical study of quantitative dactyloscopy and dermatologic signs in families with Down's syndrome]. / Statistická studie kvantitativních daktyloskopických a dermatoglyfických znaku v rodinách s morbus Down.

[Dermatoglyphic findings in families with spontaneous abortions]. / Dermatoglyfické nálezy v rodinách se spontánními potraty.

[The mosaic form of Down's syndrome]. / Mozaiková forma Downova syndromu.