DIE INNEREN WUERMZEITLICHEN SANDER IN SCHLESWIG-HOLSTEIN. = LES FORMATIONS SABLEUSES INTERIEURES WURMIENNES DU SCHLESWIG-HOLSTEINGRIPP K.1976; MEYNIANA; ALLEM.; DA. 1976; VOL. 28; PP. 29-32; H.T. 1; ABS. ANGL.; BIBL. 7 REF.Article

NEUE FUNDE AUS DEM MIOZAEN UND PLIOZAEN VON AMRUM UND SYLT.GRIPP K.1968; MEYNIANA; DEU; 1968(10), VOL. 18, P. 1 A 8Miscellaneous

EISRANDSTUDIEN, AUSGEHEND VON SERMEQ, SW-GROENLAND. = ETUDE DES BORDURES GLACIAIRES, A PARTIR DE L'EXEMPLE DE SERMEQ, SW DU GROENLANDGRIPP K.1975; MEDD. GR NONONLAND; DANM.; 1975, VOL. 195, NUM. 0008, P. 1 A 19Serial Issue

HOCHSANDER-SATRMORAENE-ENDMORAENENVERTRETER. = SABLES SUPERIEURS MORAINES EN SERIE, RESTES DE MORAINES FRONTALESGRIPP K.1975; Z. GEOMORPHOL.; DTSCH.; 1975, VOL. 19, NUM. 0004, P. 490 A 496Serial Issue

0 ANS D'ETUDES SUR CE QUI SE PASSE A LA BORDURE DE LA CALOTTE GLACIAIRE DE L'EUROPE SEPTENTRIONALEGRIPP K.1975; EISZEITALTER U. GEGENW.; DTSCH.; DA. 1975; VOL. 26; PP. 31-73; H.T. 8; ABS. ANGL.; BIBL. 4 P.; 13 ILL.Article

FOSSILIEN AUS NORDDEUTSCHLAND. (FOSSILES DU NORD DE L'ALLEMAGNE).GRIPP K.1969; MEYNIANA; DEU; 1969, VOL. 19, P. 80 A 89Miscellaneous

UNTERMORAENE-GRUNDMORAENE-GRUNDMORAENENLANDSCHAFT. = MORAINE INFERIEURE-MORAINE DE FOND-PAYSAGE DU AUX MORAINES DE FONDGRIPP K.1974; EISZEITALTER U. GEGENW.; DTSCH.; 1974, VOL. 25, P. 5 A 9Serial Issue

TROPFENBOEDEN, RAEUMLICH UNTERSUCHT. = STRUCTURES D'INVOLUTION; DESCRIPTION SPATIALE.GRIPP K.1971; MEYNIANA; DEU; 1971, VOL. 21, P. 9 A 16Miscellaneous

Der Ablauf der Würm-Vereisung in der Senkungszone am Südrand Skandinaviens = Le processus de glaciation du Würm dans la zone d'affaissement en bordure sud de la ScandinavieGRIPP, K.Meyniana. 1981, Vol 33, pp 9-22, issn 0076-7689Article

EINE PREHNIT ENTHALTENDE MEHRFACH-BRECCIE ALS EISZEIT-GESCHIEBE. = UNE BRECHE A PREHNITE: DES BLOCS ERRATIQUESGRIPP K; TUFAR W.1975; MEYNIANA; DTSCH.; 1975, VOL. 27, P. 15 A 18Serial Issue

Glazigene Press-Schuppen, frontal und lateral. in Moraines and varves. Origin/Genesis/Classification. (Lames de poussée glacigènes, frontales et latérales)GRIPP, K; SCHLUCHTER, C.1979, pp 157-166, isbn 90-6191-039-0, isbn 90-6191-039-0Book

Apparently new syndrome of congenital cataracts, sensorineural deafness, Down-syndrome-like facial appearance, short stature, and mental retardationGRIPP, K. W; NICHOLSON, L; SCOTT, C. I et al.American journal of medical genetics. 1996, Vol 61, Num 4, pp 382-386, issn 0148-7299Article

Common fragile sites in couples with recurrent spontaneous abortionsSCHLEGELBERGER, B; GRIPP, K; GROTE, W et al.American journal of medical genetics. 1989, Vol 32, Num 1, pp 45-51, issn 0148-7299, 7 p.Article

Chiari malformation and tonsillar ectopia in twin brothers and father with autosomal dominant spondylo-epiphyseal dysplasia tardaGRIPP, K. W; SCOTT, C. I; NICHOLSON, L et al.Skeletal radiology. 1997, Vol 26, Num 2, pp 131-133, issn 0364-2348Article

Decreased elastin deposition and high proliferation of fibroblasts from Costello syndrome are related to functional deficiency in the 67-kD elastin-binding proteinHINEK, A; SMITH, A. C; CUTIONGCO, E. M et al.American journal of human genetics. 2000, Vol 66, Num 3, pp 859-872, issn 0002-9297Article

TWIST gene mutation in a patient with radial aplasia and craniosynostosis : Further evidence for heterogeneity of Baller-Gerold syndromeGRIPP, K. W; STOLLE, C. A; CELLE, L et al.American journal of medical genetics. 1999, Vol 82, Num 2, pp 170-176, issn 0148-7299Article

Diaphragmatic hernia-exomphalos-hypertelorism syndrome : A new case and further evidence of autosomal recessive inheritanceGRIPP, K. W; DONNAI, D; CLERICUZIO, C. L et al.American journal of medical genetics. 1997, Vol 68, Num 4, pp 441-444, issn 0148-7299Article

Aphallia as part of urorectal septum malformation sequence in an infant of a diabetic motherGRIPP, K. W; BARR, M. JR; ANADIOTIS, G et al.American journal of medical genetics. 1999, Vol 82, Num 5, pp 363-367, issn 0148-7299Article

Chromosomal mapping of the genes GPRK5 and GPRK6 encoding G protein-coupled receptor kinases GRK5 and GRK6BULLRICH, F; DRUCK, T; BENOVIC, J. L et al.Cytogenetics and cell genetics. 1995, Vol 70, Num 3-4, pp 250-254, issn 0301-0171Conference Paper

Identification of a genetic cause for isolated unilateral coronal synostosis : A unique mutation in the fibroblast growth factor receptor 3GRIPP, K. W; MCDONALD-MCGINN, D. M; GAUDENZ, K et al.The Journal of pediatrics. 1998, Vol 132, Num 4, pp 714-716, issn 0022-3476Article

Imaging studies in a unique familial dysmyelinating disorderGRIPP, K. W; ZIMMERMAN, R. A; WANG, Z. J et al.American journal of neuroradiology. 1998, Vol 19, Num 7, pp 1368-1372, issn 0195-6108Article

Lateral meningocele syndrome : Three new patients and review of the literatureGRIPP, K. W; SCOTT, C. I; MILLER, F et al.American journal of medical genetics. 1997, Vol 70, Num 3, pp 229-239, issn 0148-7299Article

A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndromeMUENKE, M; GRIPP, K. W; LOSKEN, H. W et al.American journal of human genetics. 1997, Vol 60, Num 3, pp 555-564, issn 0002-9297Article

Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndromeSHEEN, V. L; JANSEN, A; VAID, R. R et al.Neurology. 2005, Vol 64, Num 2, pp 254-262, issn 0028-3878, 9 p.Article