au.\*:("MEINECKE P")
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DAS WAARDENBURG SYNDROM TYP I AUTOSOMAL DOMINANT ERBLICHE KOMBINATION MULTIPLER FAZIALER ANOMALIEN MIT INNENOHRSCHWERHOERIGKEIT = LE SYNDROME DE WAARDENBURG DE TYPE I, ASSOCIATION A TRANSMISISON AUTOSOMIQUE DOMINANTE D'ANOMALIES FACIALES MULTIPLES AVEC SURDITE DE L'OREILLE INTERNEMEINECKE P.1982; KLIN. PAEDIATR.; ISSN 0300-8630; DEU; DA. 1982; VOL. 194; NO 2; PP. 112-116; ABS. ENG; BIBL. 24 REF.Article
Confirmation of a particular but nonspecific metacarpophalangeal pattern profile in patients with the Smith-Magenis Syndrome due to interstitial deletion of 17pMEINECKE, P.American journal of medical genetics. 1993, Vol 45, Num 4, pp 441-442, issn 0148-7299Article
Syndrome identification case report 113: unmasked as an example of the martin-bell (fragile X) syndromeMEINECKE, P.Dysmorphology and clinical genetics. 1989, Vol 3, Num 2, pp 54-55Article
Evidence that the neurofibromatosis-Noonan syndrome is a variant of von Recklinghausen neurofibromatosisMEINECKE, P.American journal of medical genetics. 1987, Vol 26, Num 3, pp 741-745, issn 0148-7299Article
PARTIELLE TRISOMIE 18 (TRISOMIE 18 P) ALS FOLGE EINER FAMILIAEREN BALANCIERTEN TRANSLOKATION T(14;18) = TRISOMIE 18 PARTIELLES (TRISOMIE 18 P) DUE A UNE TRANSLOCATION FAMILIALE BALANCEE T(14;18)MEINECKE P; KOSKE WESTPHAL T.1981; KLIN. PAEDIATR.; ISSN 0300-8630; DEU; DA. 1981; VOL. 193; NO 6; PP. 433-438; ABS. ENG; BIBL. 24 REF.Article
RING CHROMOSOME 15 IN A MALE ADULT WITH RADIAL DEFECTS. EVALUATION OF THE PHENOTYPEMEINECKE P; KOSKE WESTPHAL T.1980; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1980; VOL. 18; NO 6; PP. 428-433; BIBL. 1 P.Article
Multiple malformation syndrome including cleft lip and palate and cardiac abnormalities due to an interstitial deletion of chromosome 12qMEINECKE, P; MEINECKE, R.Journal of medical genetics. 1987, Vol 24, Num 3, issn 0022-2593, 187Article
The Fryns syndrome: diaphragmatic defects, craniofacial dysmorphism, and distal digital hypoplasia: further evidence for autosomal recessive inheritanceMEINECKE, P; FRYNS, J. P.Clinical genetics. 1985, Vol 28, Num 6, pp 516-520, issn 0009-9163Article
Intrauterine growth retardation, mild frontonasal dysplasia, phocomelic upper limbs with absent thumbsMEINECKE, P; PEPER, M.Genetic counseling. 1992, Vol 3, Num 1, pp 53-56, issn 1015-8146Article
A specific syndrome due to deletion of the distal long arm of chromosome 1MEINECKE, P; VOGTEL, D.American journal of medical genetics. 1987, Vol 28, Num 2, pp 371-376, issn 0148-7299Article
Brief historical note on the Brachmann-de Lange syndrome : a patient closely resembling the case described by Brachmann in 1916MEINECKE, P; HAYEK, H.American journal of medical genetics. 1990, Vol 35, Num 3, pp 449-450, issn 0148-7299Article
Fetal brain disruption sequence: a milder variantBONNEMANN, C. G; MEINECKE, P.Journal of medical genetics. 1990, Vol 27, Num 4, pp 273-274, issn 0022-2593, 2 p.Article
Orofaciodigital syndrome type IV (Mohr-Majewski syndrome) with severe expression expanding the known spectrum of anomaliesMEINECKE, P; HAYEK, H.Journal of medical genetics. 1990, Vol 27, Num 3, pp 200-202, issn 0022-2593Article
Fehlbildungs-Retardierungssyndrom infolge inkompletter Triploidie = Syndrome de malformations-arriération dû à une triploïdie incomplète = Multiple congenital anomalies/mental retardation syndrome due to incomplete triploidyMEINECKE, P; ENGELBRECHT, R.Monatsschrift für Kinderheilkunde. 1988, Vol 136, Num 4, pp 206-209, issn 0026-9298Article
Bilateral porencephaly, cerebellar hypoplasia, and internal malformations : Two siblings representing a probably new autosomal recessive entityBÖNNEMANN, C. G; MEINECKE, P.American journal of medical genetics. 1996, Vol 63, Num 3, pp 428-433, issn 0148-7299Article
Encephalopathy of infancy with intracerebral calcification and chronic spinal fluid lymphocytosis - another case of the aicardi-goutières syndromeBÖNNEMANN, C. G; MEINECKE, P.Neuropediatrics. 1992, Vol 23, Num 3, pp 157-161, issn 0174-304XArticle
FG-Syndrom bei zwei HalbbrüdernWIEG, C; MEINECKE, P.Monatsschrift für Kinderheilkunde. 1991, Vol 139, Num 10, pp 687-689, issn 0026-9298Conference Paper
Encephalopathy with intracerebral calcification, white matter lesions, growth hormone deficiency, microcephaly, and retinal degeneration : two sibs confirming a probably distinct entityBÖNNEMANN, C. G; MEINECKE, P; REICH, H et al.Journal of medical genetics. 1991, Vol 28, Num 10, pp 708-711, issn 0022-2593Article
Further delineation of the ichthyosis follicularis, atrichia, and photophobia syndromeHAMM, H; MEINECKE, P; TRAUPE, H et al.European journal of pediatrics. 1991, Vol 150, Num 9, pp 627-629, issn 0340-6199Article
Kniepterygium-Syndrom bei einem Neugeborenen = Syndrome de pterygium poplité chez un nouveau-né = Popliteal pterygium syndrome in a newbornMEINECKE, P; MENZEL, J; FROSTER-ISKENIUS, U et al.Monatsschrift für Kinderheilkunde. 1989, Vol 137, Num 4, pp 228-230, issn 0026-9298Article
Limb anomalies in the CHARGE associationMEINECKE, P; POLKE, A; SCHMIEGELOW, P et al.Journal of medical genetics. 1989, Vol 26, Num 3, pp 202-203, issn 0022-2593, 2 p.Article
Coffin-Siris-Syndrom bei einem 5jährigen Mädchen = Coffin Siris syndrome chez une fillette de 5 ans = The Coffin Siris syndrome in a 5 years old girlMEINECKE, P; ENGELBRECHT, R; SCHAEFER, E et al.Monatsschrift für Kinderheilkunde. 1986, Vol 134N9, pp 692-695, issn 0026-9298Article
Normal hands and feet in the ulnar-mammary syndromeMEINECKE, P; STIER, U; BLUNCK, W et al.Dysmorphology and clinical genetics. 1989, Vol 3, Num 3, pp 61-64, 4 p.Article
Cerebro-costo-mandibuläres Syndrom ohne cerebrale Beteiligung bei einem 4 jährigen Jungen = Syndrome cérébrocostomandibulaire sans atteinte cérébrale chez un garçon de 4 ans = Cerebrocostomandibular syndrome without cerebral involvement in a 4 years old boyMEINECKE, P; WOLFF, G; SCHAEFER, E et al.Monatsschrift für Kinderheilkunde. 1987, Vol 135, Num 1, pp 54-58, issn 0026-9298Article
Balanced t(6;8)(6p8p;6q8q) and the CHARGE associationHURST, J. A; MEINECKE, P; BARAITSER, M et al.Journal of medical genetics. 1991, Vol 28, Num 1, pp 54-55, issn 0022-2593, 2 p.Article